|Integrin alpha6Bbeta4 inhibits colon cancer cell proliferation and c-Myc activity.|
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|PMID: 19586553 Owner: NLM Status: MEDLINE|
|BACKGROUND: Integrins are known to be important contributors to cancer progression. We have previously shown that the integrin beta4 subunit is up-regulated in primary colon cancer. Its partner, the integrin alpha6 subunit, exists as two different mRNA splice variants, alpha6A and alpha6B, that differ in their cytoplasmic domains but evidence for distinct biological functions of these alpha6 splice variants is still lacking. METHODS: In this work, we first analyzed the expression of integrin alpha6A and alpha6B at the protein and transcript levels in normal human colonic cells as well as colorectal adenocarcinoma cells from both primary tumors and established cell lines. Then, using forced expression experiments, we investigated the effect of alpha6A and alpha6B on the regulation of cell proliferation in a colon cancer cell line. RESULTS: Using variant-specific antibodies, we observed that alpha6A and alpha6B are differentially expressed both within the normal adult colonic epithelium and between normal and diseased colonic tissues. Proliferative cells located in the lower half of the glands were found to predominantly express alpha6A, while the differentiated and quiescent colonocytes in the upper half of the glands and surface epithelium expressed alpha6B. A relative decrease of alpha6B expression was also identified in primary colon tumors and adenocarcinoma cell lines suggesting that the alpha6A/alpha6B ratios may be linked to the proliferative status of colonic cells. Additional studies in colon cancer cells showed that experimentally restoring the alpha6A/alpha6B balance in favor of alpha6B caused a decrease in cellular S-phase entry and repressed the activity of c-Myc. CONCLUSION: The findings that the alpha6Bbeta4 integrin is expressed in quiescent normal colonic cells and is significantly down-regulated in colon cancer cells relative to its alpha6Abeta4 counterpart are consistent with the anti-proliferative influence and inhibitory effect on c-Myc activity identified for this alpha6Bbeta4 integrin. Taken together, these findings point out the importance of integrin variant expression in colon cancer cell biology.|
|Anders Bondo Dydensborg; Inga C Teller; Jean-François Groulx; Nuria Basora; Fréderic Paré; Elizabeth Herring; Rémy Gauthier; Dominique Jean; Jean-François Beaulieu|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2009-07-09|
|Title: BMC cancer Volume: 9 ISSN: 1471-2407 ISO Abbreviation: BMC Cancer Publication Date: 2009|
|Created Date: 2009-07-27 Completed Date: 2009-12-11 Revised Date: -|
Medline Journal Info:
|Nlm Unique ID: 100967800 Medline TA: BMC Cancer Country: England|
|Languages: eng Pagination: 223 Citation Subset: IM|
|CIHR Team on the Digestive Epithelium, Department of Anatomy and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Québec, J1H 5N4, Canada. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Aged, 80 and over
Cell Line, Tumor
Colonic Neoplasms / metabolism*, therapy
Epithelial Cells / cytology
Fluorescent Antibody Technique, Indirect
Gene Expression Regulation, Neoplastic*
Integrin alpha6beta4 / metabolism, physiology*
Proto-Oncogene Proteins c-myc / metabolism*
RNA, Messenger / metabolism
|0/Integrin alpha6beta4; 0/Proto-Oncogene Proteins c-myc; 0/RNA, Messenger|
Journal ID (nlm-ta): BMC Cancer
Publisher: BioMed Central
Copyright © 2009 Dydensborg et al; licensee BioMed Central Ltd.
open-access: This is an Open Access article distributed under the terms of the Creative Commons Attribution License (), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received Day: 27 Month: 1 Year: 2009
Accepted Day: 9 Month: 7 Year: 2009
collection publication date: Year: 2009
Electronic publication date: Day: 9 Month: 7 Year: 2009
Volume: 9First Page: 223 Last Page: 223
Publisher Id: 1471-2407-9-223
PubMed Id: 19586553
|Integrin α6Bβ4 inhibits colon cancer cell proliferation and c-Myc activity|
|Anders Bondo Dydensborg1||Email: firstname.lastname@example.org|
|Inga C Teller1||Email: email@example.com|
|Jean-François Groulx1||Email: firstname.lastname@example.org|
|Nuria Basora1||Email: email@example.com|
|Fréderic Paré1||Email: firstname.lastname@example.org|
|Elizabeth Herring1||Email: email@example.com|
|Rémy Gauthier1||Email: firstname.lastname@example.org|
|Dominique Jean1||Email: email@example.com|
|Jean-François Beaulieu1||Email: Jean-Francois.Beaulieu@USherbrooke.ca|
1CIHR Team on the Digestive Epithelium, Department of Anatomy and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Québec, J1H 5N4, Canada
Integrins are heterodimeric, transmembrane receptors composed of an α and a β subunit that transmit signals from extracellular matrix components to the cell interior. Integrins do not possess intrinsic signalling capacities, but rather mediate positional information by interacting with a large range of scaffolding proteins resulting in activation of several signalling molecules, such as Ras and PI3K, leading to subsequent activation of, among other molecules, JNK, Jun, Erk and CyclinD . The net result of this integrin mediated intracellular signalling is control of cellular functions such as proliferation, migration, invasion and survival, all of which are pivotal events in cancer progression . The existence of 18 α subunits and 8 β subunits leads to the formation of at least 24 distinct integrins, which are further diversified by extensive alternative splicing and post-translational modifications .
The accumulated findings of an association between high expression levels of the α6 integrin subunit and carcinoma cell invasion, metastatic capacity, apoptosis evasion and negative patient outcome [4-6] strongly argue in favor of a role for α6 containing integrins in human cancers. While the α6 subunit can dimerize with either β1 or β4 subunits, it preferentially dimerizes with the β4 subunit. In fact, in cells that express significant amounts of β4, such as human intestinal epithelial cells , the formation of α6β1 is nominal. Recent work from our laboratory has demonstrated an overall up-regulation of the expression of the β4 integrin subunit in primary tumors of the human colon  strongly supporting the notion that the α6β4 integrin is an important player in the migration and invasion of colon cancer cells [4,9]. These observations, taken together with the reported presence of this major laminin receptor at the invasive front of colorectal cancers , argue for an important role for the α6β4 integrin in colon cancer progression .
The α6 integrin subunit exists as two distinct variants, α6A and α6B, that differ in their cytoplasmic domains as the result of alternative splicing of a single exon . Thus, the inclusion of an alternatively spliced exon results in the formation of the α6A variant, while exclusion leads to a reading frame shift, use of an alternative stop codon and formation of the α6B variant. These two variants show dissimilar spatial and temporal patterns of expression in various human organs and tissues [13,14]. For example, the α6A variant is exclusive to the mammary gland, basal keratinocytes and peripheral nerves, while the α6B variant is strongly favored in the kidney . These distinct expression patterns, in combination with the conservation of the two variants in all mammalian species studied, suggest a biological importance for the existence of both molecules . These arguments are supported by the divergent capacities of the α6A and -B subunits to initiate intracellular biochemical events, namely tyrosine phosphorylation of paxillin  and activation of the Ras-MEK-ERK pathway . However, further evidence for the biological role of these α6 integrin splice variants is still lacking.
In the present study, we sought to establish the expression patterns and possible functions of the α6A and α6B integrin subunits in the normal human and adenocarcinoma cells of the colon. Our data show that these two variants are differentially expressed according to cell state. The A variant was predominant in the progenitor cells of the normal colon while the B variant was predominant in mature differentiated colonocytes. Significantly, we show a diminishment of α6B variant expression in primary colon carcinomas and adenocarcinoma cell lines. Interestingly, forced expression of the α6B variant revealed a specific ability of this variant to inhibit colonocyte proliferation and c-Myc activity.
Samples of adult colon were obtained from patients between the ages of 49 and 86 years undergoing surgical treatment for colon adenocarcinoma. For each patient, samples from the primary tumor and from non-diseased areas (at least 10 cm distant from the lesion) corresponding to the resection margin were obtained. Diagnoses of adenocarcinoma were confirmed by pathologists. Staging of the carcinomas was according to Astler and Coller . Resection margins of colon specimens obtained from patients undergoing surgery for pathologies other than colon cancer (bowel obstruction, diverticulosis, etc.) were also used for immunofluorescence. All tissues were obtained in accordance with protocols approved by the local Institutional Human Research Review Committee for the use of human material. The preparation and embedding of tissues for cryosectioning and RNA extraction was performed as described previously . Additional paired samples (resection margin and confirmed carcinomas) were obtained from the Cooperative Human Tissue Network (Midwestern Division, Ohio State University, OH) which is funded by the National Cancer Institute.
Cryosections 3 μm thick were fixed in 2% paraformaldehyde (α6A, Ki67 and Rbm19) or -20°C ethanol (α6B). Nonspecific protein-protein interactions were blocked for one hour at room temperature by immersion of slides in 10% goat serum (α6A) or 2% BSA (α6B) in PBS followed by incubation with the primary antibodies diluted 1:200 in their respective blocking solutions overnight at room temperature. Following extensive washing in PBS, the slides were incubated with either FITC or rhodamine conjugated secondary antibodies raised against mouse and rabbit IgG (Chemicon), respectively, for one hour at room temperature before being washed in PBS. The slides were stained with Evan's blue (0.01% in PBS) before being mounted in glycerol:PBS (9:1) containing 0.1% paraphenylenediamine and observed for fluorescence with a Leica Reichart Polyvar 2 microscope (Leica Canada, Saint-Laurent, QC) equipped with a Leica DFC300 FX digital color camera. In all cases, no immunofluorescent staining was observed when a mix of mouse and rabbit non-immune sera replaced primary antibodies.
Two antibodies recognizing integrin α6A (1A10) and α6B (6B4)  were originally generous gifts from Dr. A. Sonnenberg (Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands). Subsequently, these antibodies were obtained from Chemicon (Temecula, CA; 1A10) and MUbio Products (Maastricht, The Netherlands; 6B4). Mabs 1A10 and 6B4 were used for western blots and co-immunoprecipitation. For indirect immunofluorescence, 6B4 and a rabbit polyclonal α6A (α6-cytoA)  antibody was obtained and employed in place of 1A10. This antibody was a generous gift from Dr. de Curtis (Department of Molecular Pathology and Medicine, San Raffaele Scientific Institute, Milan, Italy). The anti-Ki67 monoclonal antibody KiS5 and the polyclonal anti-lysozyme antiserum were from Chemicon and DAKO Cytomation (Glostrup, Denmark). The anti-progenitor cell Rbm19 antibody  was a kind gift from Dr. Alan M. Mayer (Department of Pediatrics, Medical College of Wisconsin, WI). To probe for β-actin, the antibody C4 from Chemicon was employed.
The c-Myc responsive luciferase reporter plasmid, pMyc-TA-Luc (Clontech, Mountain View, CA), carries six c-Myc binding sequences in front of the minimal TATA box from the herpes simplex thymidine kinase (HSV-TK) promoter. An Rb responsive luciferase reporter plasmid, pRb-TA-Luc (Clontech) was also used. An expression vector containing the cDNA of integrin α6A, pRc/CMV-α6A , was a generous gift from Dr. Sonnenberg (Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands). The α6A cDNA was subcloned into the viral expression vector pLPCX (BD Bioscience Clontech, Mississauga, ON) by a non-directional strategy using Hind III. Correct orientation was verified by restriction enzyme analysis. cDNA originating from a preparation of fetal epithelial enterocytes separated from the mesenchyme using Matrisperse (BD Biosciences, Mississauga, ON) as described previously  was used as a template for PCR amplification of the cytoplasmic tail of the α6B subunit using Pwo polymerase (Roche, Laval, QC). The upstream primer (5' TGCTGAAAGAAAATACCAGA 3') spanned an endogenous XbaI site, while the downstream primer (5' GC TCTAGAGAAAAAGCAGTTTGGGTACT 3') introduced another (underlined sequence.) The amplified DNA was ligated into pPCR-Script (Stratagene, La Jolla, CA) and verified for fidelity by sequencing. Subsequently, the cDNA encoding the cytoplasmic tail of the integrin α6A subunit in pRc/CMV-α6A was replaced by the cDNA encoding the cytoplasmic tail of the integrin α6B subunit by XbaI digestion of the recipient (pRc/CMV-α6A) and donor (pPCR-Script-α6B) vectors followed by ligation, generating pRc/CMV-α6B. The cDNA encoding the integrin α6B subunit was subcloned into the pLPCX vector using the same strategy as for α6A. A mammalian episomal expression vector, pEEP1, was used to generate populations of Caco-2/15 cells over-expressing the two integrin α6 splice variants. Integrin α6A or α6B subunit cDNA was excised from pRc/CMV-α6A and pRc/CMV-α6B, respectively, using HindIII, Klenow filled and blunt-end ligated into a Klenow filled NotI site in pEEP1, generating pEEP1-α6A and pEEP1-α6B.
The colon cancer cell line, Caco-2/15 was grown in DMEM (GIBCO, Burlington, ON) supplemented with 10% fetal bovine serum (ICN Biomedicals, Aurora, OH), 1% HEPES and 1% Glutamax (both from GIBCO, Burlington, ON) as described previously . The colon cancer cell lines HT-29, COLO 201, DLD-1, HCT 116, T84, SW480 and SW620 were grown in accordance with instructions provided by the ATCC (Rockville, MD). All cells were grown in an atmosphere of 95% air and 5% CO2 at 37°C.
The pEEP1-α6A and pEEP1-α6B plasmids were introduced into 1 × 106 Caco-2/15 cells by nucleofection using the Amaxa Biosystem Nucleofection kit (ESBE Scientific, St. Laurent, QC) using the T-20 setting. Immediately following nucleofection, the cells were seeded onto collagen coated cell culture dishes (Falcon, Franklin Lakes, NJ). 24 hours post-nucleofection the cells were subjected to hygromycin (Multicell, St. Bruno, QC) selection at a concentration of 200 μg/ml for 10 days. This selection pressure was maintained throughout the experimental period to ensure continuous replication and transfer of the episomal plasmid. Forced expression of the α6A and α6B subunits was monitored by western blot.
BrdU incorporation and staining was performed according to the manufacturer's (Roche Applied Science, Laval, QC) instructions. Briefly, 24 hours after plating of cells in LabTeks (Nalge Nunc, Rochester, NY) the cells were incubated for two hours with normal medium containing BrdU then immediately subjected to anti-BrdU and DAPI staining. For each condition, two random fields per well were counted for DAPI and BrdU positive cells and the BrdU positive cell population was determined as a percentage of total DAPI positive cells. All experiments were performed in quadruplicate and repeated three times.
Western blots were performed as SDS-PAGE under non-denaturing conditions using 120 μg of whole cell lysate per lane. After transfer of the separated samples to a nitrocellulose membrane (BioRad, Hercules, CA) unspecific protein binding to the membrane was blocked by 5% skim milk-powder in PBS-0.1% Tween followed by incubation with the α6A 1A10 monoclonal antibody. Following detection, the membrane was stripped of antibody by incubation in stripping solution (50 mM Tris (pH 6.8), 2% SDS, 100 mM β-mercaptoethanol) at 50°C for 20 minutes after which the membrane was reprobed with the α6B 6B4 antibody using 2% BSA/0.1% Tween as blocking solution. Finally, the membrane was restripped and reprobed with a β-actin antibody as input control.
For immunoprecipitation of α6β4 and α6β1, newly confluent Caco-2/15 cells and keratinocytes (a kind gift of Dr L. Germain, LOEX, Université Laval, Québec, QC) were metabolically labeled using Promix [35S]methionine and cystine (Amersham Pharmacia Biotech), 200 μCi/ml for 6 h. Cells were lysed and processed as previously described  for immunoprecipitation of α6-containing integrins with the antibody G0H3 and Protein-G Sepharose (Invitrogen). Radioactive samples were analyzed under reduced and nonreduced conditions by SDS PAGE .
First strand cDNA synthesis was performed with 2 μg total RNA using oligo(dT)12–18 (Amersham Pharmacia, Bay d'Urfé, QC) as primer and Omniscript reverse transcriptase (Qiagen, Mississauga, ON) for synthesis. Primers used to co-amplify the α6A and α6B transcripts using 1/50 of the synthesized cDNA above were sense: 5'-CTAACGGAGTCTCACAACTC-3' and antisense: 5'-AGTTAAAACTGTAGGTTCG-3'. Each cycle was composed of template denaturation at 94°C for 1 minute, primer annealing at 65°C for 1 minute and elongation at 72°C for 1 minute. The primer annealing temperature was decreased by 0.5°C after each round of amplification for 40 cycles followed by a final 15 cycles at an annealing temperature of 45°C.
Quantitative RT-PCR was performed as previously described). Three different primer pairs for the integrin α6 subunit were tested for amplification efficiency and fidelity. The primer pair termed α6PD-2 was chosen for amplification of cDNA coding for the integrin α6 subunit based on a superior amplification efficiency and lack of primer dimer formation as assessed by melting curve analysis. The Ct-values were converted into relative expression values compared to a pooled RNA standard (QPCR Human Reference Total RNA, Stratagene, La Jolla, CA) before normalization of α6 expression against a weighted average of three normalizing genes (B2M, MTR & MAN1B1) using the geNorm applet . Briefly, this algorithm normalizes a gene of interest against several normalizing genes, rather than against a single gene, thus obtaining an analysis of expression that is less likely to be impacted by any random fluctuations in the expression level of the normalizing gene(s). The sequences of the α6PD-2 primer were: sense 5' TGGGATATGCCTCCAGGTT 3', antisense 5' TGTAGCCACAGGGTTTCCTC 3'. Primer pairs for B2M, MAN1B1, and MTR have been described previously). The annealing temperatures of the reactions were 57°C (α6) or 58°C (B2M, MAN1B1 and MTR) and the amplification efficiencies of the reactions were 100.7%, 105.7%, 98.9% and 96.8% for α6, B2M, MTR and MAN1B1, respectively, as determined by standard curve analysis.
Equal numbers of Caco-2/15 cells were seeded in 24-well plates (Falcon, Franklin Lakes, NJ) and grown to 40–60% confluence before being transiently transfected in serum-free medium using FuGENE transfection agent (Roche, Indianapolis, IN) in a μg DNA to μl transfection agent ratio of 1:9. Cells were kept under normal growth conditions after transfection and harvested for analysis 48 hours post-transfection. All transfections were performed as co-transfections using a renilla luciferase expression plasmid to establish an internal control for transfection efficiency; thus allowing for normalization of cell number and viability. Promoter activities of the various reporter plasmids were expressed using the arbitrary unit "RLU" (relative luciferase units). Numeric values of CMV promoters in control transfections (empty vector) were kept equal to experimental (α6A and α6B) numeric values by adjusting the absolute level of plasmid as measured by μg. DNA concentrations in transfections were kept constant with the addition of pBluescript SK+ (Stratagene, Cedar Creek, TX). Equal amounts (25 ng) of reporter plasmid and expression vector (pRc/CMV-α6A and pRc/CMV-α6B) were cotransfected with 2 ng of pCMV-Renilla per well. Firefly and renilla luciferase activity was measured using the Dual-Luciferase® Reporter Assay System (Promega Corporation, Madison, WI) according to the manufacturer's instructions using an Orion microplate luminometer from Berthold (Montreal Biotech, Kirkland, QC) for detection of the chemiluminescent signal. Individual experimental results were normalized to the average of the RLU of the empty vector cotransfectant in the corresponding experiment.
We previously showed the ubiquitous presence of the α6 dimerization partner β4 along the glandular unit of the human colon . We, therefore, proceeded directly to delineate the specific expression patterns of the α6A and α6B splice variants in the normal human adult colonic mucosa (Figure 1). The α6A subunit was expressed in the basal membrane of epithelial cells concentrated in the lower half of the glands (Figure 1A), a region that contains the progenitor cells as identified by co-immunodetection with the proliferative antigens Ki67 and Rbm19 (Figure 1B, C, G, H, I). Staining for the α6B subunit on serial sections revealed its presence in the epithelium located in the upper half of the glands and at the base of the surface epithelium (Figure 1D, E), while it was not detected in the lower crypt (Figure 1F). The association of α6A with the actively growing cell population and α6B with the mature differentiated population supports the hypothesis that each variant possesses a specific distinct function, necessary for intestinal homeostasis.
The α6β4 integrin is frequently up-regulated in several cancer types . As in our previous study on the β4 subunit , using quantitative PCR we observed a significant up-regulation of total α6 expression in paired primary tumor samples versus patient matched normal resection margins (RM) (Figure 2A). We then assessed whether modulation of α6 splice-variant expression accompanied the overall up-regulation of total α6 in primary tumors. Competitive RT-PCR using primers that amplify the transcripts of both α6 variants showed an overall dominance of α6B expression in the healthy resection margins (Figure 2B – RM). Furthermore, a clear down-regulation of expression of the α6B variant in conjunction with a possible increase in the α6A variant were observed in patient matched tumors (Figure 2B, C). Overall, 81% of the 21 pairs showed the same change in expression in the tumor sample, resulting in a statistically significant shift towards a diminished α6B/A-ratio in primary cancers compared to healthy resection margins (Figure 2D). However, no correlation was noted between tumor grade or stage and α6B down-regulation (data not shown). A predominant expression of the α6B variant in normal colonic tissue is in accordance with the fact that the quiescent cell population outsizes the proliferative cell population in the normal colon. Correspondingly, a shift towards higher expression of the A variant in hyperproliferative colon carcinomas correlated with the association of this variant with the proliferative compartment of the healthy colon.
The patterns of expression of α6A and α6B were analyzed in situ by indirect immunofluorescence on 8 primary tumors and their corresponding resection margins (Figure 3). All specimens were well- to moderately-differentiated tumors. In all examined resection margins the differential distribution of α6A in the lower half of the gland and α6B in the upper half of the gland and in the surface epithelium was comparable to that observed in normal colon specimens (data not shown). Analyses of frozen serial sections from primary tumors revealed that the A variant was now found almost ubiquitously expressed at the base of carcinoma cells (Figure 3A, C, E, and 3G) while the B variant was detected in most, but not all, corresponding regions (Figure 3B, D, F and 3H). These results exposed the widespread overlap of expression between the two α6 variants in colon cancer epithelia suggesting the loss of segregated expression found in normal colon tissue. In addition, extensive expression of α6A in carcinoma cells was consistent with the observed up-regulation of α6A at the transcript level (Figure 2B, D).
We next investigated the relative α6A and α6B levels in 6 well established colon cancer cell lines to see if this characteristic was conserved. All six cell lines tested predominantly expressed the A-variant (Figure 4A). However, at least one exception to this exists since the Colo 320 cell line has been previously shown to predominantly express the B-variant  suggesting that, as observed herein for the primary tumors where 4 out of the 21 pairs analyzed did not show an α6A subunit increase (Figure 2D), the relation between high α6A expression and a pro-proliferative state is not absolute in colon cancer cell lines of human origin although quite frequent. To further investigate the phenomenon, we used the two colon cancer cell lines, Caco-2/15 and HT-29 that share the trait of undergoing a differentiation program, characterized by a significant decline in proliferation, as a consequence of culture method. These two cell types express both β1 and β4 subunits but because the affinity of α6 for β4 is much greater than for β1, it can be assumed based on studies performed on keratinocytes and other cell types that the α6A/B variants mainly combine with β4 [7,13,26]. This was confirmed by immunoprecipitating the α6B complex from metabolically labeled Caco-2/15 or primary keratinocytes with [35S] methionine and cystine using the α6 subunit-specific G0H3 antibody and analysis by SDS-PAGE under reduced and non-reduced conditions. As shown in Figure 4B, both keratinocytes and Caco-2/15 cells display bands at approximately 205 kD and 150 kD and 205 kD and 120 kD corresponding to the β4 and α6 subunits under non-reduced and reduced conditions, respectively. The β1 subunit remained below detection level in Caco-2/15 cells confirming that α6 predominantly associates with β4 in intestinal cells. We thus used the two intestinal cell models Caco-2/15 and HT-29 to monitor the expression of the α6A and B variants during the course of proliferation arrest accompanied by the induction of differentiation. Competitive RT-PCR revealed that the ratio of α6A to α6B was altered as a function of cell state, reflecting the situation in vivo. Higher levels of α6A were associated with actively growing cells and a subsequent switch in favour of α6B was found to be associated with cells that had undergone cell cycle arrest (Figure 4C, D). This trend was mirrored in protein levels as well when detected with variant specific antibodies (Figure 3E).
Elevated levels of unligated integrins can provoke intracellular signalling resulting in apoptosis . Consequently, we focused our experiments on the well-characterized colon cancer cell line Caco-2/15 which has the ability to constitutively deposit significant amounts of laminins , the α6β4 ligands. To evaluate the hypothesis that an altered α6A/α6B ratio could be of functional importance for the proliferative status of colon cancer cells we attempted to create stable cell lines over-expressing α6A and α6B. However, we were repeatedly unable to maintain the α6B cells in long term cultures suggesting that over-expression of the α6B variant impaired cell proliferation. We were unable to perform complementary studies using RNAi since the only difference between the mRNA of the α6A and α6B variants is the inclusion of an alternatively spliced exon in the α6A transcript. As no region of the transcript is unique to the α6B variant it was not possible to exclusively target the α6B transcript for RNAi.
We consequently opted to perform studies on nucleofected cell populations over-expressing the two variants despite the difficulty in maintaining the α6B over-expressing cells, analyzing the cells shortly following the 10-day antibiotic selection period ensuring that all cells expressed their respective episomal vectors (Figure 5A). Proliferation was assessed using BrdU incorporation assays. With this strategy we consistently observed that the proportion of α6B transfectants entering S-phase was significantly diminished compared to the α6A transfectants and the empty vector control (Figure 5B), suggesting that predominant expression of the α6B subunit inhibits S-phase entry in intestinal epithelial cells in accordance with the predominant expression of this subunit in the non-proliferative compartment of the colon and it's relative down-regulation in colon carcinomas. Consistent with these observations, a specific reduction in transcriptional Rb activity was observed in luciferase assays (Figure 6A) supporting the observation that the α6B-expressing cells are exiting cell cycle in G1 .
Colon cancer cells and glandular proliferative cells require the activity of the proto-oncogene c-Myc for proliferation . We next evaluated the ability of the α6B subunit to modulate c-Myc activity by performing co-transfections of the two integrin α6 variants with a luciferase reporter plasmid responding to c-Myc activity (pMyc-Ta-Luc). Experiments performed in colon cancer cells (Caco-2/15) demonstrated that pMyc-TA-luc activity was significantly down-regulated by α6B over-expression (Figure 6B), but was not altered by α6A. The decrease in c-Myc activity in the α6B co-transfections was not due to any changes in c-Myc protein levels as determined by western blot analyses (Fig 6C).
The functional importance of the instructive interactions between the epithelial cell compartment with the surrounding extracellular milieu has long been recognized in the intestinal tract [31,32]. Our observations that the α6A and α6B splice variants are differentially expressed in progenitor and mature cells of the colonic epithelium, located in the lower and upper half of the glands respectively , are consistent with previous findings showing the existence of distinct microenvironments between the proliferative and differentiation compartments in the gut [7,34]. More importantly, it suggests that the intrinsic role of each α6 variant is distinct. In this context, our finding that the α6B variant exclusively repressed proliferation concurs with its low level of expression in the proliferative zone and its predominance in the non-proliferative compartments of the colon as shown herein, as well as in the small intestine . The effect of the α6B variant on cell proliferation in vitro appeared sufficient to prevent expansion of these cultures although the potential low grade contribution of apoptosis or autophagy cannot be excluded at the present time.
Colon cancer is the third leading cause of cancer related mortality in the United States . The occurrence and development of most colon cancers follows a stereotypical pattern of a progressive accumulation of gain- and loss of function mutations of oncogenes and tumor suppressor genes . It is also clear that neoplastic cells tend to up-regulate the expression of integrins favoring their migration, survival and proliferation during the complex multistep generation of tumors . The mechanistic and biochemical roles of the α6β4 integrin in carcinoma biology are well documented[4,38]. Our results describe novel aspects of the biology of the α6β4 integrin variants in colon cancer. Thus, after having identified that distinct forms of the integrin β4 subunit were expressed in normal intestinal proliferative vs cancer cells , we observed herein a shift in α6 variant expression from a predominantly high α6B/α6A ratio in the normal colon to a predominantly low α6B/α6A ratio in primary tumors.
c-Myc is a key player in cancer formation and progression due to the numerous roles it plays in proliferation control and apoptosis . Indeed, c-Myc expression has been demonstrated to be up-regulated in 70% of colon cancers  and its well documented effects include stimulation of cyclinD expression, inhibition of p21cip1 and p27kip1 expression and inactivation of Rb, leading to enhanced G1 to S-phase transition . Given the central role of c-Myc in the control of critical cellular events, its transcriptional functions are tightly regulated by several molecular pathways . Prototypically, the control of cellular c-Myc levels are largely attributed to the canonical activity of the Wnt-pathway . However, the activity and expression levels of c-Myc are regulated by several other molecular mechanisms including distinct signalling pathways and interaction with binding partners [39,43]. For instance, the nucleoshuttling scaffold protein bridging integrator-1 (Bin1) has been shown to strongly inhibit c-Myc transcriptional activity in a Wnt-pathway independent manner [44,45]. Interestingly, Bin1 can selectively interact with the cytoplasmic domain of the α6B integrin subunit in yeast two-hybrid studies  and its expression has been reported to be associated with the non-proliferative cell population in the normal intestine  suggesting a possible mechanism for the inhibitory effect of α6Bβ4 on c-Myc activity.
While there is substantial evidence for the differential capacity of the α6Aβ1 and α6Bβ1 integrins to initiate intracellular signalling [15,16] and facilitate migration on laminin , these studies have all found that the α6Aβ1 integrin functions as the "active" integrin, whereas the α6Bβ1 integrin appears to have no major active role in these events [15,16,48-50]. In this context it is noteworthy that over-expression of the α6A variant in colon cancer cells did not stimulate proliferation as compared to the control cells, but rather the α6B variant actively inhibited proliferation and c-Myc activity, under conditions where integrin/ligand interactions occurred. It is furthermore noteworthy that the α6A/B splice variants can dimerize with both the β1 and the β4 subunits to form two distinct functional integrins, α6β1 and α6β4, but that the α6 subunit preferentially dimerizes with the β4 subunit [7,13,26], as confirmed herein. Thus, the specific ability of the α6B subunit to inhibit proliferation, in accordance with its predominant expression in the quiescent compartment of the normal colon and its down-regulation in primary colon cancers and adenocarcinoma cell lines, strongly suggests that the expression and ratio of the α6A and α6B splice variants are inherent to normal intestinal homeostasis and exploited by colon cancer cells.
In this study, we provide the first functional evidence that the α6Bβ4 integrin can exert distinct biological functions compared to its α6Aβ4 counterpart. Analyzing the expression of the two α6 variants in the human normal colon led to the discovery that the A and the B variants are differentially expressed in proliferative and differentiated cells, respectively. More significantly, a net shift toward a predominant A variant expression was observed in primary colorectal tumors and in adenocarcinoma cell lines suggesting that a high α6A/B ratio is required for both normal and cancer cell proliferation. To test this hypothesis, we forced α6A and α6B expression and found that re-establishing predominant α6B subunit expression inhibited colon cancer cell proliferation and c-Myc activity. Taken together, these findings point out the importance of integrin variant expression in colon cancer cell biology.
The authors declare that they have no competing interests.
ABD carried out most of the cell and molecular biology studies and drafted the manuscript. ICT carried out the immunofluorescence and related experimental set-up. JFG participated in the luciferase assays and immunofluorescence of the colon cancer specimens. NB carried out the immunoprecipitation studies and participated in the writing of the manuscript. FP participated with the luciferase and BrdU assays. RG performed the proliferation studies. DJ designed the episomal vectors. JFB conceived the study, participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
The authors thank Drs. J. Gosselin, M. Lessard and J. Poisson (CHUSherbrooke) for their cooperation in providing matched colon cancer specimens and pathological expertise. We acknowledge the collaboration of the Cooperative Human Tissue Network, funded by the National Cancer Institute, in obtaining additional sets of matched colon cancer specimens. We are particularly grateful to Drs. A. Sonnenberg, I. de Curtis and A.M. Mayer, for sharing antibodies and/or constructs.
The work was supported by the Canadian Institutes of Health Research Grants MOP 62914 (to JFB). JFB is the recipient of a Canadian Research Chair in Intestinal Physiopathology and a member of the FRSQ-funded Centre de Recherche Clinique Étienne Lebel of the CHUS. ABD was supported by a studentship from the Danish Agency for Science, Technology and Innovation (642-02-0055).
|Giancotti FG,Tarone G. Positional control of cell fate through joint integrin/receptor protein kinase signalingAnnu Rev Cell Dev Biol 2003;19:173–206. [pmid: 14570568]|
|Guo W,Giancotti FG. Integrin signalling during tumour progressionNat Rev Mol Cell Biol 2004;5:816–826. [pmid: 15459662]|
|de Melker AA,Sonnenberg A. Integrins: alternative splicing as a mechanism to regulate ligand binding and integrin signaling eventsBioessays 1999;21:499–509. [pmid: 10402956]|
|Mercurio AM,Rabinovitz I. Towards a mechanistic understanding of tumor invasion – lessons from the alpha6beta 4 integrinSemin Cancer Biol 2001;11:129–141. [pmid: 11322832]|
|Friedrichs K,Ruiz P,Franke F,Gille I,Terpe HJ,Imhof BA. High expression level of alpha 6 integrin in human breast carcinoma is correlated with reduced survivalCancer Res 1995;55:901–906. [pmid: 7850807]|
|Chung J,Mercurio AM. Contributions of the alpha6 integrins to breast carcinoma survival and progressionMol Cells 2004;17:203–209. [pmid: 15179031]|
|Basora N,Herring-Gillam FE,Boudreau F,Perreault N,Pageot LP,Simoneau M,Bouatrouss Y,Beaulieu JF. Expression of functionally distinct variants of the beta(4)A integrin subunit in relation to the differentiation state in human intestinal cellsJ Biol Chem 1999;274:29819–29825. [pmid: 10514460]|
|Ni H,Dydensborg AB,Herring FE,Basora N,Gagne D,Vachon PH,Beaulieu JF. Upregulation of a functional form of the beta4 integrin subunit in colorectal cancers correlates with c-Myc expressionOncogene 2005;24:6820–6829. [pmid: 16007143]|
|Pouliot N,Nice EC,Burgess AW. Laminin-10 mediates basal and EGF-stimulated motility of human colon carcinoma cells via alpha(3)beta(1) and alpha(6)beta(4) integrinsExp Cell Res 2001;266:1–10. [pmid: 11339819]|
|Lohi J,Oivula J,Kivilaakso E,Kiviluoto T,Frojdman K,Yamada Y,Burgeson RE,Leivo I,Virtanen I. Basement membrane laminin-5 is deposited in colorectal adenomas and carcinomas and serves as a ligand for alpha3beta1 integrinApmis 2000;108:161–172. [pmid: 10752684]|
|Mercurio AM,Bachelder RE,Rabinovitz I,O'Connor KL,Tani T,Shaw LM. The metastatic odyssey: the integrin connectionSurg Oncol Clin N Am 2001;10:313–328. viii-ix. [pmid: 11382589]|
|Hogervorst F,Kuikman I,van Kessel AG,Sonnenberg A. Molecular cloning of the human alpha 6 integrin subunit. Alternative splicing of alpha 6 mRNA and chromosomal localization of the alpha 6 and beta 4 genesEur J Biochem 1991;199:425–433. [pmid: 2070796]|
|Hogervorst F,Admiraal LG,Niessen C,Kuikman I,Janssen H,Daams H,Sonnenberg A. Biochemical characterization and tissue distribution of the A and B variants of the integrin alpha 6 subunitJ Cell Biol 1993;121:179–191. [pmid: 7681434]|
|Thorsteinsdottir S,Roelen BA,Freund E,Gaspar AC,Sonnenberg A,Mummery CL. Expression patterns of laminin receptor splice variants alpha 6A beta 1 and alpha 6B beta 1 suggest different roles in mouse developmentDev Dyn 1995;204:240–258. [pmid: 8573717]|
|Shaw LM,Turner CE,Mercurio AM. The alpha 6A beta 1 and alpha 6B beta 1 integrin variants signal differences in the tyrosine phosphorylation of paxillin and other proteinsJ Biol Chem 1995;270:23648–23652. [pmid: 7559532]|
|Wei J,Shaw LM,Mercurio AM. Regulation of mitogen-activated protein kinase activation by the cytoplasmic domain of the alpha6 integrin subunitJ Biol Chem 1998;273:5903–5907. [pmid: 9488728]|
|Astler VB,Coller FA. The prognostic significance of direct extension of carcinoma of the colon and rectumAnn Surg 1954;139:846–851. [pmid: 13159135]|
|Beaulieu JF. Differential expression of the VLA family of integrins along the crypt-villus axis in the human small intestineJ Cell Sci 1992;102:427–436. [pmid: 1506425]|
|de Curtis I,Reichardt LF. Function and spatial distribution in developing chick retina of the laminin receptor alpha 6 beta 1 and its isoformsDevelopment 1993;118:377–388. [pmid: 8223267]|
|Lorenzen JA,Bonacci BB,Palmer RE,Wells C,Zhang J,Haber DA,Goldstein AM,Mayer AN. Rbm19 is a nucleolar protein expressed in crypt/progenitor cells of the intestinal epitheliumGene Expr Patterns 2005;6:45–56. [pmid: 16027046]|
|Delwel GO,Hogervorst F,Kuikman I,Paulsson M,Timpl R,Sonnenberg A. Expression and function of the cytoplasmic variants of the integrin alpha 6 subunit in transfected K562 cells. Activation-dependent adhesion and interaction with isoforms of lamininJ Biol Chem 1993;268:25865–25875. [pmid: 8245021]|
|Perreault N,Beaulieu JF. Primary cultures of fully differentiated and pure human intestinal epithelial cellsExp Cell Res 1998;245:34–42. [pmid: 9828099]|
|Beaulieu JF,Quaroni A. Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cellsBiochem J 1991;280:599–608. [pmid: 1764023]|
|Dydensborg AB,Herring E,Auclair J,Tremblay E,Beaulieu JF. Normalizing genes for quantitative RT-PCR in differentiating human intestinal epithelial cells and adenocarcinomas of the colonAm J Physiol Gastrointest Liver Physiol 2006;290:G1067–1074. [pmid: 16399877]|
|Vandesompele J,De Preter K,Pattyn F,Poppe B,Van Roy N,De Paepe A,Speleman F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genesGenome Biol 2002;3:RESEARCH0034. [pmid: 12184808]|
|Hemler ME,Crouse C,Sonnenberg A. Association of the VLA alpha 6 subunit with a novel protein. A possible alternative to the common VLA beta 1 subunit on certain cell linesJ Biol Chem 1989;264:6529–6535. [pmid: 2649503]|
|Stupack DG,Cheresh DA. Get a ligand, get a life: integrins, signaling and cell survivalJ Cell Sci 2002;115:3729–3738. [pmid: 12235283]|
|Vachon PH,Beaulieu JF. Extracellular heterotrimeric laminin promotes differentiation in human enterocytesAm J Physiol 1995;268:G857–867. [pmid: 7539221]|
|Harbour JW,Dean DC. Rb function in cell-cycle regulation and apoptosisNat Cell Biol 2000;2:E65–67. [pmid: 10783254]|
|Wetering, M van de;Sancho, E.;Verweij, C.;de Lau, W.;Oving, I.;Hurlstone, A.;Horn, K van der;Batlle, E.;Coudreuse, D.;Haramis, AP.,et al. The beta-catenin/TCF-4 complex imposes a crypt progenitor phenotype on colorectal cancer cellsCell 2002;111:241–250. [pmid: 12408868]|
|Beaulieu JF. Extracellular matrix components and integrins in relationship to human intestinal epithelial cell differentiationProg Histochem Cytochem 1997;31:1–78. [pmid: 9088045]|
|Teller IC,Beaulieu JF. Interactions between laminin and epithelial cells in intestinal health and diseaseExpert Rev Mol Med 2001;3:1–18. [pmid: 14585148]|
|Babyatsky M,Podolsky D. Yamada TGrowth and development in the gastrointestinal tractTextbook of Gastroenterology Volume 1 (2) 1995;Chapter 232. Philadelphia, USA: Lippincott, Williams and Wilkins; :475–501.|
|Basora N,Vachon PH,Herring-Gillam FE,Perreault N,Beaulieu JF. Relation between integrin alpha7Bbeta1 expression in human intestinal cells and enterocytic differentiationGastroenterology 1997;113:1510–1521. [pmid: 9352853]|
|Dydensborg AB,Teller IC,Basora N,Groulx JF,Auclair J,Francoeur C,Escaffit F,Paré F,Herring E,Ménard D,Beaulieu JF. Differential expression of the integrin alpha6Abeta4 and alpha6Bbeta4 along the crypt-villus axis in the human small intestineHistochem Cell Biol 2009;131:531–536. [pmid: 19107504]|
|Jemal A,Siegel R,Ward E,Hao Y,Xu J,Murray T,Thun MJ. Cancer statistics, 2008CA Cancer J Clin 2008;58:71–96. [pmid: 18287387]|
|Radtke F,Clevers H. Self-renewal and cancer of the gut: two sides of a coinScience 2005;307:1904–1909. [pmid: 15790842]|
|Shaw LM,Rabinovitz I,Wang HH,Toker A,Mercurio AM. Activation of phosphoinositide 3-OH kinase by the alpha6beta4 integrin promotes carcinoma invasionCell 1997;91:949–960. [pmid: 9428518]|
|Adhikary S,Eilers M. Transcriptional regulation and transformation by Myc proteinsNat Rev Mol Cell Biol 2005;6:635–645. [pmid: 16064138]|
|Erisman MD,Rothberg PG,Diehl RE,Morse CC,Spandorfer JM,Astrin SM. Deregulation of c-myc gene expression in human colon carcinoma is not accompanied by amplification or rearrangement of the geneMol Cell Biol 1985;5:1969–1976. [pmid: 3837853]|
|Cole MD,Nikiforov MA. Transcriptional activation by the Myc oncoproteinCurr Top Microbiol Immunol 2006;302:33–50. [pmid: 16620024]|
|Clevers H. Wnt/beta-catenin signaling in development and diseaseCell 2006;127:469–480. [pmid: 17081971]|
|Sakamuro D,Prendergast GC. New Myc-interacting proteins: a second Myc network emergesOncogene 1999;18:2942–2954. [pmid: 10378691]|
|Elliott K,Sakamuro D,Basu A,Du W,Wunner W,Staller P,Gaubatz S,Zhang H,Prochownik E,Eilers M,Prendergast GC. Bin1 functionally interacts with Myc and inhibits cell proliferation via multiple mechanismsOncogene 1999;18:3564–3573. [pmid: 10380878]|
|Kinney EL,Tanida S,Rodrigue AA,Johnson JK,Tompkins VS,Sakamuro D. Adenovirus E1A oncoprotein liberates c-Myc activity to promote cell proliferation through abating Bin1 expression via an Rb/E2F1-dependent mechanismJ Cell Physiol 2008;216:621–631. [pmid: 18348166]|
|Wixler V,Laplantine E,Geerts D,Sonnenberg A,Petersohn D,Eckes B,Paulsson M,Aumailley M. Identification of novel interaction partners for the conserved membrane proximal region of alpha-integrin cytoplasmic domainsFEBS Lett 1999;445:351–355. [pmid: 10094488]|
|DuHadaway JB,Lynch FJ,Brisbay S,Bueso-Ramos C,Troncoso P,McDonnell T,Prendergast GC. Immunohistochemical analysis of Bin1/Amphiphysin II in human tissues: diverse sites of nuclear expression and losses in prostate cancerJ Cell Biochem 2003;88:635–642. [pmid: 12532338]|
|Ferletta M,Kikkawa Y,Yu H,Talts JF,Durbeej M,Sonnenberg A,Timpl R,Campbell KP,Ekblom P,Genersch E. Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activationMol Biol Cell 2003;14:2088–2103. [pmid: 12802077]|
|Shaw LM,Mercurio AM. Regulation of alpha 6 beta 1 integrin-mediated migration in macrophagesAgents Actions Suppl 1995;47:101–106. [pmid: 7785489]|
|Gimond C,Baudoin C,Neut R van der,Kramer D,Calafat J,Sonnenberg A. Cre-loxP-mediated inactivation of the alpha6A integrin splice variant in vivo: evidence for a specific functional role of alpha6A in lymphocyte migration but not in heart developmentJ Cell Biol 1998;143:253–266. [pmid: 9763436]|
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