|ZAK negatively regulates RhoGDIbeta-induced Rac1-mediated hypertrophic growth and cell migration.|
|Jump to Full Text|
|PMID: 19538723 Owner: NLM Status: MEDLINE|
|RhoGDIbeta, a Rho GDP dissociation inhibitor, induced hypertrophic growth and cell migration in a cultured cardiomyoblast cell line, H9c2. We demonstrated that RhoGDIbeta plays a previously undefined role in regulating Rac1 expression through transcription to induce hypertrophic growth and cell migration and that these functions are blocked by the expression of a dominant-negative form of Rac1. We also demonstrated that knockdown of RhoGDIbeta expression by RNA interference blocked RhoGDIbeta-induced Rac1 expression and cell migration. We demonstrated that the co-expression of ZAK and RhoGDIbeta in cells resulted in an inhibition in the activity of ZAK to induce ANF expression. Knockdown of ZAK expression in ZAK-RhoGDIbeta-expressing cells by ZAK-specific RNA interference restored the activities of RhoGDIbeta.|
|Chih-Yang Huang; Li-Chiu Yang; Kuan-Yu Liu; I-Chang Chang; Pao-Hsin Liao; Janet Ing-Yuh Chou; Ming-Yung Chou; Wei-Wen Lin; Jaw-Ji Yang|
Related Documents :
|23698633 - Pertuzumab counteracts the inhibitory effect of erbb2 on degradation of erbb3.
23486593 - Manifestation of multidrug resistance protein 3 (mrp3) in liver and kidney cells in cho...
15111313 - Tumor necrosis factor-alpha induces fractalkine expression preferentially in arterial e...
|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2009-06-18|
|Title: Journal of biomedical science Volume: 16 ISSN: 1423-0127 ISO Abbreviation: J. Biomed. Sci. Publication Date: 2009|
|Created Date: 2009-06-30 Completed Date: 2009-09-01 Revised Date: 2013-06-02|
Medline Journal Info:
|Nlm Unique ID: 9421567 Medline TA: J Biomed Sci Country: England|
|Languages: eng Pagination: 56 Citation Subset: IM|
|Graduate Institute of Chinese Medical Science, China Medical University, Taichung 404, Taiwan. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Guanine Nucleotide Dissociation Inhibitors / genetics, metabolism*
Protein Kinases / metabolism*
rac1 GTP-Binding Protein / metabolism*
rho-Specific Guanine Nucleotide Dissociation Inhibitors
|0/Guanine Nucleotide Dissociation Inhibitors; 0/rho-Specific Guanine Nucleotide Dissociation Inhibitors; EC 2.7.-/Protein Kinases; EC 188.8.131.52/rac1 GTP-Binding Protein|
Journal ID (nlm-ta): J Biomed Sci
Publisher: BioMed Central
Copyright © 2009 Huang 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: 15 Month: 6 Year: 2008
Accepted Day: 18 Month: 6 Year: 2009
collection publication date: Year: 2009
Electronic publication date: Day: 18 Month: 6 Year: 2009
Volume: 16 Issue: 1
First Page: 56 Last Page: 56
Publisher Id: 1423-0127-16-56
PubMed Id: 19538723
|ZAK negatively regulates RhoGDIβ-induced Rac1-mediated hypertrophic growth and cell migration|
|Chih-Yang Huang123||Email: firstname.lastname@example.org|
|Li-Chiu Yang456||Email: email@example.com|
|Kuan-Yu Liu4||Email: KYLiu@imb.sinica.edu.tw|
|I-Chang Chang7||Email: firstname.lastname@example.org|
|Pao-Hsin Liao46||Email: email@example.com|
|Janet Ing-Yuh Chou8||Email: firstname.lastname@example.org|
|Ming-Yung Chou46||Email: email@example.com|
|Wei-Wen Lin9||Email: firstname.lastname@example.org|
|Jaw-Ji Yang4||Email: email@example.com|
1Graduate Institute of Chinese Medical Science, China Medical University, Taichung 404, Taiwan
2Graduate Institute of Basic Medical Science, China Medical University, Taichung 404, Taiwan
3Department of Health and Nutrition Biotechnology, Asia University, Taichung 413, Taiwan
4School of Dentistry, Chung-Shan Medical University, Taichung 402, Taiwan
5Institute of Medicine, Chung-Shan Medical University, Taichung 402, Taiwan
6Chung-Shan Medical University Hospital, Chung-Shan Medical University, Taichung 402, Taiwan
7Department of Orthopedics Surgery, Chung-Shan Medical University, Taichung 402, Taiwan
8Midwestern University Chicago College of Osteopathic Medicine, Chicago, USA
9Cardiovascular Center, Veterans General Hospital, Taichung 407, Taiwan
The mitogen-activated protein kinase (MAPK) signaling pathway consists of the sequentially acting upstream kinases MAPK kinase kinase (MAP3K) and MAPK kinase (MAP2K), and the downstream MAPKs, p38MAPK, extracellular signal-regulated kinase (ERK1/2), and c-jun N-terminal kinase (JNK). The mixed lineage kinases are a family of serine/threonine kinases, all of which are classified as MAP3Ks. The seven mixed lineage kinases cloned over the past several years can be classified into three subfamilies based on domain organization and sequence similarity: the MLKs (MLK1–4), the dual leucine zipper-bearing kinases (DLK and LZK), and the zipper sterile-α-motif (SAM) kinases (ZAKα and ZAKβ) [1,2]. ZAK can activate the JNK pathway and the nuclear factor κB (NFκB) pathway , and it induces JNK activation through a dual phosphorylation kinase, JNKK2/MKK7 . Overexpression of wild-type ZAK induced apoptosis in a hepatoma cell line , and a recent report indicated that ZAK expression in a rat cardiac cell line, H9c2, induced hypertrophic growth and re-expression of atrial natriuretic factor (ANF) . ZAK also mediates TGF-β-induced cardiac hypertrophic growth via a novel TGF-β signaling pathway . In our previous study , we showed that the leucine zipper of ZAK mediates homodimerization and promotes autophosphorylation and JNK activation.
We identified RhoGDIβ(Rho GDP dissociation inhibitor beta) as a ZAK effector. RhoGDIβ, also known as Ly-GDI or D4-GDI, belongs to a family of Rho GDP dissociation inhibitors, and it is thought to regulate the activity and localization of Rho family proteins [7-10]. The RhoGTPase family includes Rho, Rac, and Cdc42, which differentially regulate the actin cytoskeleton [11-13] and function as molecular switches in cellular signal transduction by alternating between an inactive GDP-bound form that is maintained in cytosolic complexes with GDIs and a GTP-bound form that usually associates with the plasma membrane and interacts with downstream target proteins therein [14,15]. RhoGTPases regulate the reorganization of the actin cytoskeleton and the integrity of the integrin-associated adhesion complexes . Rho facilitates stress fiber and focal adhesion assembly, Rac regulates the formation of lamellipodia and membrane ruffles at the leading edge of migrating cells, and Cdc42 triggers filopodia at the cell periphery . RhoGDIs regulate RhoGTPase activity by inhibiting GDP dissociation to keep RhoGTPases in an inactive state.
A recent study indicated that stimulation of T lymphocytes and myelomonocytic cells with phorbol esters leads to RhoGDIβ phosphorylation on serine/threonine residues , raising the question of whether RhoGDIβ is involved in a signal transduction pathway in these cells. Thus, RhoGDIβ may play numerous roles in the regulation of biological activities; however, many details of the regulatory roles of RhoGDIβ remain to be elucidated.
Trizol reagents (Life Technologies) were used to isolate total RNA from H9c2 cells transiently transfected with the recombinant RhoGDIβ plasmids or from cells stably expressing RhoGDIβ. Total RNA (20 μg) was separated on a formaldehyde agarose gel, transferred to a nylon filter, and then hybridized with a probe corresponding to the full-length Rac1 cDNA labeled using the NEBlot random labeling kit (New England BioLabs) in the presence of [α-32P]dCTP. The blot was washed with SSC/SDS solutions (Sodium Chloride, Sodium Citrate/SDS) before autoradiography. Ethidium bromide staining was used to check the integrity of all samples.
H9c2 cells seeded on 10-cm plates were cultured to confluency. They were then scratched with a 200 μl pipette tip and further incubated in DMEM supplemented with 10% FBS. Images were taken at 24, 48, and 72 h with a Zeiss Axiovert 200 microscope. The Image-Pro image analysis system was used to measure the lesion area. The data were expressed as the percentage of recovery (WC%) using the equation: WC% = [1 - (wounded area at Tt/wounded area at T0)] × 100%, where Tt is the number of hours post-injury and T0 is the time of injury.
H9c2 cells were cultured with 1 μg/ml doxycycline for 48 h and then treated with lysis buffer (20 mM Tris-HCl, pH 7.5, 100 mM NaCl, 5 mM EDTA, 2 mM PMSF, 1× protease inhibitor) at 4°C for 30 min. The samples were centrifuged at 500 × g at 4°C for 10 min, and the pellets were dissolved in lysis buffer plus 0.1% (w/v) Triton X-100 for the membrane fractions. The supernatants were re-centrifuged at 15,000 rpm at 4°C for 20 min, and the supernatants were saved as cytosolic fractions.
The RhoGTPases act as molecular switches by cycling between the inactive GDP-bound form located in the cytoplasm and an active membrane-associated GTP-bound form. The activities of Rho family proteins are regulated by various proteins, such as guanine nucleotide exchange factors (GEFs), GTPase activating proteins (GAPs), and GDIs. The functions and binding of RhoGDIα to RhoA, Rac1, and Cdc42 are well studied; however, the functions and targets for RhoGDIβ remain unclear, as it binds poorly to RhoA, Rac1, and Cdc42. We therefore sought to determine whether RhoGDIβ stimulates the expression or activities of these GTPases in cardiac cells by western blotting. The total RhoA and Cdc42 levels remained the same; however, cells overexpressing RhoGDIβ had increased levels of Rac1 (Figure 1A). Moreover, the expression of RhoGDIα in H9c2 cells was not affected by the overespression RhoGDIβ (Figure 1A). The expression levels of Rac1 may be causally linked to RhoGDIβ expression or merely an epiphenomenon of the selection of a stable clone. If the former is the case, then Rac1 might be a functionally important downstream target of RhoGDIβ. Northern blot analysis of total RNA indicated that cardiac cells either stably or transiently overexpressing RhoGDIβ had increased Rac1 mRNA levels (Figure 1B). We therefore concluded that RhoGDIβ plays a role in the transcriptional regulation of Rac1 and that the increased level of Rac1 mRNA was not a secondary effect of the selection of a stable RhoGDIβ-expressing clone. Rac1 association with membranes reflects its biological activity . To further address the question of whether induction of Rac1 may also influence Rac1 activity, a detergent-insoluble membrane fraction was prepared from RhoGDIβ-overexpressing cells, and the levels of membrane-associated Rac1 were determined by western blotting. Both the levels of membrane-associated Rac1 and cytosolic Rac1 increased in RhoGDIβ-overexpressing cells (Figure 1C). Furthermore, the membrane-associated and cytosolic forms of Cdc42 remained unchanged in RhoGDIβ-expressing cells when compared to parental cells. We further detect the amount of GTP-bound Rac1 in H9c2 RhoGDIβ-overexpressing cells. We found that RhoGDIβ increased GTP loading in Rac1 (Figure 1D). Therefore, overexpression of RhoGDIβ in H9c2 cells increases the level of membrane-associated Rac1 and GTP loading in RAC1 by upregulating Rac1 transcripts. However, the increase in membrane-associated Rac1 in RhoGDIβ-expressing cells may be a secondary effect of increased expression of Rac1, as we were not able to detect any physical interaction between RhoGDIβ and Rac1 by co-immunoprecipitation.
We next examined whether Rac1 mediates RhoGDIβ-induced hypertrophic growth. We found that H9c2 cells stably expressing a dominant-negative form of Rac1 (Rac1N17) and RhoGDIβ significantly reduced the twofold increase in cell size (Figure 2A) and actin organization induced by RhoGDIβ. Moreover, overexpression of wild-type or a constitutively active (V12) Rac1 in H9c2 cells was sufficient to induce hypertrophic growth (Figure 2A) and actin organization. These findings indicate that the RhoGDIβ-induced hypertrophic growth in H9c2 cells is mediated through increased expression of Rac1, and probably through increased levels of membrane-associated Rac1.
Rac1 is able to regulate cell migration . To test whether the effect of RhoGDIβ on cell migration is Rac1 dependent, confluent monolayers of cells stably expressing RhoGDIβ, RhoGDIβ and Rac1, or RhoGDIβ and Rac1N17 were scrape-wounded with a sterile plastic pipette, and the migration of cells into the wound was monitored. The RhoGDIβ-expressing cells closed the wound area faster than control cells (Figure 2B). RhoGDIβ-expressing cells that also expressed a dominant-negative form of Rac1N17 migrated slower than RhoGDIβ-expressing or RhoGDIβ- and Rac1-expressing cells (Figure 2B), suggesting that Rac1 plays a key role in mediating cell migration in RhoGDIβ-expressing cells.
To determine whether Rac1 might play a role in the RhoGDIβ-mediated cell cycle arrest, we examined the growth rate of cells expressing both RhoGDIβ and Rac1N17 and found that it was substantially slower than the growth rate of RhoGDIβ-expressing cells or control cells (Additional file 1). Therefore, the RhoGDIβ-regulated cell arrest was not mediated through increased levels of membrane-bound active Rac1.
Since the cyclin-dependent kinase inhibitors p21Waf1/Cip1 and p27Kip1 were expressed in RhoGDIβ-expressing cells at higher levels than they were in control cells, we examined p21Waf1/Cip1 and p27Kip1 levels in RhoGDIβ- and Rac1N17-expressing cells to study the effects of this dominant-negative form of Rac1 on the expression of p21 and p27. RacN17 was unable to block the expression of p21Waf1/Cip1 and p27Kip1 induced by RhoGDIβ in H9c2 cardiac cells (Additional file 2), suggesting that the RhoGDIβ-induced cell cycle arrest was not mediated through Rac1.
To this point, our results indicated that RhoGDIβ stimulates cell migration through the induction of Rac1 expression due to a proportional increase in the activity of Rac1 in H9c2 cells. To confirm the role of RhoGDIβ in cell migration, two RhoGDIβ knockdown cell lines were used to assess whether RhoGDIβ directly stimulates Rac1 expression to induce cell migration. The specific knockdown of RhoGDIβ using siRNA in H9c2 cells was confirmed by immunoblotting (Fig. 2C). We found that targeted disruption of RhoGDIβ by siRNA effectively blocked expression of Rac1 (Fig. 2C); therefore, RhoGDIβ depletion is associated with Rac1 downregulation. We used migration assays to confirm the role of RhoGDIβ in cell migration. Cells were seeded in an upper chamber of a Transwell on a porous filter, and the migration through the filter pores of H9c2 cells expressing RhoGDIβ and cells expressing both RhoGDIβ and RhoGDIβ- specific siRNA was compared. RhoGDIβ-expressing cells showed increased migration compared to parental cells, whereas migration was inhibited in the siRNA RhoGDIβ knockdown cells relative to the RhoGDIβ-expressing cells (Additional file 3). These results suggest that RhoGDIβ may play a critical role in the regulation of Rac1 expression and H9c2 cell migration.
Our experiments demonstrated that RhoGDIβ increased the rate of wound closure. However, our data also suggested that the physical association of ZAK with RhoGDIβ and phosphorylation of RhoGDIβ by ZAK could abolish RhoGDIβ function. To identify the regulatory role of ZAK on cell migration responses in RhoGDIβ-expressing cells, a wound-healing assay was performed using cells expressing RhoGDIβ, ZAK and RhoGDIβ, or ZAKdn and RhoGDIβ. After wounding, control, ZAK-expressing, and ZAKdn-expressing cells closed the gap at a similar rate (Figure 3A). As demonstrated above, RhoGDIβ-expressing cells were highly migratory, but ZAK- and RhoGDIβ-expressing cells were substantially slower to close the wound than ZAKdn- and RhoGDIβ-expressing cells. At 36 h post-wounding, control, ZAK-expressing, ZAKdn-expressing, and ZAK- and RhoGDIβ-expressing cells closed the gap by about 20%, 24%, 25%, and 22%, respectively (Figure 3B). RhoGDIβ-expressing cells and ZAKdn- and RhoGDIβ-expressing cells closed 50% and 39% of the gap. These data suggested a negative regulatory role for ZAK in RhoGDIβ cell migratory function.
To elucidate the role of RhoGDIβ in controlling the localization of Rac1, we performed confocal microscopy. The majority of Rac1 was present in the perinuclear region with some present at the plasma membrane of the control, ZAK-expressing, and ZAKdn-expressing cells (Additional file 4). More Rac1 was present at both the plasma membrane and the perinuclear region in RhoGDIβ-expressing cells. However, co-expression of ZAK, but not ZAKdn, with RhoGDIβ in H9c2 cardiac cells decreased the amount of Rac1 at the plasma membrane (Additional file 4). These data also suggested that ZAK might decrease the total amount of cellular Rac1, probably due to ZAK binding and phosphorylation of RhoGDIβ. To determine whether ZAK negatively regulates RhoGDIβ through expression of Rac1, especially membrane-associated Rac1, we performed western blotting. Consistent with the above experiment, membrane-associated Rac1 increased in RhoGDIβ-expressing cells, whereas, in ZAK- and RhoGDIβ-expressing cells, the levels of membrane-associated Rac1 decreased. However, co-expression of ZAKdn and RhoGDIβ had no such effect (Figure 4A). In this regard, it was of interest whether RhoGDIβ increases the amount of Rac1 at the plasma membrane as a consequence of increasing the total cellular levels of Rac1 or whether RhoGDIβ facilitates the translocation of Rac1 to the plasma membrane. We attempted to co-immunoprecipitate RhoGDIβ and Rac1to investigate this possibility; however, the antibody used was insufficient for this purpose (data not shown). This suggests that it is unlikely that RhoGDIβ facilitates translocation of Rac1 to the plasma membrane.
To test the importance of ZAK in regulating RhoGDIβ-mediated membrane-associated Rac1 and hypertrophic growth, we reduced the levels of ZAK using siRNA. We were able to reduce the levels of ZAK by expressing two different human ZAK siRNAs: ZAKGRi1 (ZAK-RhoGDIβ U6-460i) and ZAKGRi2 (ZAK-RhoGDIβ U6-1712i) (data not shown). The reduced levels of ZAK in these two individual clones were able to restore the levels of membrane-associated Rac1 to levels similar to those of RhoGDIβ-expressing cells, whereas the introduction of a scrambled ZAK siRNA (GRCi) into ZAK- and RhoGDIβ-expressing cells had no effect (Figure 4B). These results confirmed the importance of ZAK as a negative regulator of the effect of RhoGDIβ on the expression of Rac1 and membrane-associated Rac1. We found that ZAK was able to regulate ANF expression. We then studied the effects of RhoGDIβ on the regulation of ANF expression by ZAK by examining the levels of ANF mRNA in ZAK- and RhoGDIβ-expressing cells when compared with ZAK-expressing cells. The levels of ANF mRNA induced by ZAK were decreased in cells expressing both ZAK and RhoGDIβ (Fig. 4C). We also found that ZAK-RhoGDIβ cells has less total amount of Rac1 than RhoGDIβ cells. (Figure 4D). This result suggested that RhoGDIβ negatively regulates the functions of ZAK. Moreover, the data presented here (and consistent with our previous studies) indicate that both ZAK and RhoGDIβ may be hypertrophic growth inducers; however, ZAK physically interacts with RhoGDIβ and phosphorylates RhoGDIβ, thus inhibiting the ability of RhoGDIβ to induce Rac1 expression. The levels of Rac1 induced by RhoGDIβ are associated with the closure rate of wound healing (Figure 2B) and hypertrophic growth (Figure 2A), but they are not associated with cell cycle inhibition (Additional file 1). Thus, RhoGDIβ appears to play a role in signaling pathways regulating Rac1 expression that govern wound healing and hypertrophic growth in cardiac cells.
Upon introduction of RhoGDIβ into rat cardiac H9c2 cells, the cells exhibited hypertrophic growth, had a slower cell cycle, and migrated to a greater extent. We previously demonstrated that RhoGDIβ is phosphorylated by ZAK in vitro. It is striking that the co-expression of ZAK and RhoGDIβ in H9c2 cardiac cells results in the inhibition of the biological functions of RhoGDIβ, indicating that not only does RhoGDIβ possibly physically interact with ZAK, but it may also be negatively regulated by ZAK, and this regulation might occur via phosphorylation. These phenomena regulated by ZAK were correlated with Rac 1 expression and especially with the levels of membrane-associated Rac1 in H9c2 cells.
In H9c2 cells transiently and stably expressing RhoGDIβ, the levels of Rac1 transcripts increased compared with control cells. In this study, we described these surprising findings and, to our knowledge, the first demonstration that expression of RhoGDIβ induces Rac1 transcripts and increases the levels of membrane-associated Rac1. The results from western blotting and confocal microscopy experiments indicate that RhoGDIβ regulates Rac1 expression, which leads to increased levels of membrane-associated Rac1. We propose either that the increased levels of membrane-associated Rac1 in RhoGDIβ cells are merely a consequence of RhoGDIβ-induced expression of Rac1 or that RhoGDIβ regulates membrane translocation of Rac1. We were unable to detect an association between RhoGDIβ and Rac1 using co-immunoprecipitation; therefore, it is unlikely that RhoGDIβ andRac1 directly interact. However, we still have not ruled out the possibility that RhoGDIβ regulates Rac1 translocation. However, the signaling pathway between RhoGDIβ and Rac1 has not yet been elucidated, and there is currently no evidence that RhoGDIβ can directly bind to any gene promoter. RhoGDIβ can be translocated into the nucleus upon certain stimuli , leaving the possibility that RhoGDIβ can regulate gene expression directly. It is also possible that RhoGDIβ regulates Rac1 expression via signaling pathway effector proteins. Studies have also demonstrated that RhoGDIβ is cleaved at its N-terminus during apoptosis in a caspase-dependent manner and that the cleaved RhoGDIβ is retained in the nuclear compartment . This suggests that RhoGDIβ could function in the nucleus.
We previously found that RhoGDIβ was able to associate with a mixed lineage kinase, ZAK, resulting in the phosphorylation of RhoGDIβ. To further study the role of ZAK in regulating the activities of RhoGDIβ, we used a bi-directional tet-on inducible system to express both ZAK and RhoGDIβ in H9c2 cardiac cells. Our results demonstrate that the levels of membrane-associated Rac1 and the hypertrophic growth phenotype were inhibited by co-expression of ZAK and RhoGDIβ; however, we did not observe the inhibitory effect with a dominant-negative form of ZAK. Clearly, the kinase activities of ZAK are necessary for the negative regulation of RhoGDIβ functions, including cell cycle arrest, hypertrophic growth, alterations in the amount of membrane-associated Rac1, and cell migration. Among all the biological functions that are regulated by RhoGDIβ, the phenomena of hypertrophic growth and cell migration are Rac1-dependent, whereas the regulation of the cell cycle arrest is Rac1-independent, as shown by the results of expression of a dominant-negative Rac1 (Rac1N17) in RhoGDIβ-expressing cells. It should be pointed out that the cell migration phenotype induced in RhoGDIβ-expressing cells seems to result primarily from the rate of migration rather than cell division. Therefore, RhoGDIβ may stimulate cell migration in a manner dissociated from its effects on cell cycle progression.
The authors declare that they have no competing interests.
CYH was responsible for the pull-down assay. LCY was responsible for the SiRNA knockdown. KYL was responsible for the cell migration assay. ICC, JIY, MYC and WWL were responsible for Western blot analysis. PHL was responsible for cell staining. JJY wrote the manuscript.
Figure S1. The growth rate of H9c2 cells expressing RhoGDIβ and Rac1N17 grown in 10% fetal bovine serum with doxycycline.
Click here for additional data file (1423-0127-16-56-S1.png)
Additional file 2
Figure S2. Expression levels of cyclin-dependent kinase inhibitors p21 and p27 in H9c2 RhoGDIβ-expressing cells and H9c2 cells expressing both RhoGDIβ and Rac1N17.
Click here for additional data file (1423-0127-16-56-S2.png)
Additional file 3
Figure S3. SiRNA knockdown of RhoGDIβ inhibited cell migration of H9c2 RhoGDIβ-expressing cells.
Click here for additional data file (1423-0127-16-56-S3.png)
Additional file 4
Figure S4. Confocal microscopy of H9c2 and H9c2 cells expressing the indicated proteins.
Click here for additional data file (1423-0127-16-56-S4.png)
This work was supported by grants to J. J. Y. from the National Science Council (NSC) (NSC96-2311-B-040-003-) and M. Y. C. from the National Science Council (NSC) (NSC97-2314-B-040-024-MY2), Taiwan.
|Gallo KA,Johnson GL. Mixed-lineage kinase control of JNK and p38 MAPK pathwaysNature Rev Mol Cell Biol 2002;3:663–672. [pmid: 12209126] [doi: 10.1038/nrm906]|
|Handley ME,Rasaiyaah J,Chain BM,Katz DR. Mixed lineage kinases (MLKs): a role in dendritic cells, inflammation and immunity?Int J Exp Pathol 2007;88:111–126. [pmid: 17408454] [doi: 10.1111/j.1365-2613.2007.00531.x]|
|Liu T-C,Huang C-J,Chu Y-C,Wei C-C,Chou C-C,Chou M-Y,Chou C-K,Yang J-J. Cloning and Expression of ZAK, a Mixed Lineage Kinase-Like Protein containing a Leucine-Zipper and a Sterile-Alpha MotifBiochem Biophy Research Communications 2000;274:811–816. [doi: 10.1006/bbrc.2000.3236]|
|Yang J-J. Mixed lineage kinase ZAK utilizing MKK7 and not MKK4 to activate the c-Jun N-terminal kinase and playing a role in the cell arrestBiochem Biophy Research Communications 2002;297:105–110. [doi: 10.1016/S0006-291X(02)02123-X]|
|Huang CY,Chueh PJ,Tseng CT,Liu KY,Tsai HY,Kuo WW,Chou MY,Yang JJ. ZAK re-programs atrial natriuretic factor expression and induces hypertrophic growth in H9c2 cardiomyoblast cellsBiochem Biophys Res Commun 2004;324:973–980. [pmid: 15485649] [doi: 10.1016/j.bbrc.2004.09.156]|
|Huang CY,Kuo WW,Chueh PJ,Tseng CT,Chou MY,Yang JJ. Transforming growth factor-beta induces the expression of ANF and hypertrophic growth in cultured cardiomyoblast cells through ZAKBiochem Biophys Res Commun 2004;324:424–431. [pmid: 15465036] [doi: 10.1016/j.bbrc.2004.09.067]|
|Dovas A,Couchman JR. RhoGDI: multiple functions in the regulation of Rho family GTPase activitiesBiochem J 2005;390:1–9. [pmid: 16083425] [doi: 10.1042/BJ20050104]|
|Fauré J,Dagher MC. Interactions between Rho GTPases and Rho GDP dissociation inhibitor (Rho-GDI) Biochimie 2001;83(5):409–414. [pmid: 11368848] [doi: 10.1016/S0300-9084(01)01263-9]|
|Golovanov AP,Chuang TH,DerMardirossian C,Barsukov I,Hawkins D,Badii R,Bokoch GM,Lian LY,Roberts GC. Structure-activity relationships in flexible protein domains: regulation of rho GTPases by RhoGDI and D4 GDIJ Mol Biol 2001;305:121–135. [pmid: 11114252] [doi: 10.1006/jmbi.2000.4262]|
|Groysman M,Hornstein I,Alcover A,Katzav S. Vav1 and Ly-GDI Two Regulators of Rho GTPases, Function Cooperatively as Signal Transducers in T Cell Antigen Receptor-induced PathwaysJ Biol Chem 2002;277:50121–50130. [pmid: 12386169] [doi: 10.1074/jbc.M204299200]|
|Evers EE,Zondag GC,Malliri A,Price LS,ten Klooster JP,Kammen RA van der,Collard JG. Rho family proteins in cell adhesion and cell migrationEur J Cancer 2000;36:1269–1274. [pmid: 10882865] [doi: 10.1016/S0959-8049(00)00091-5]|
|Raftopoulou M,Hall A. Cell migration: Rho GTPases lead the wayDev Biol 2004;265:23–32. [pmid: 14697350] [doi: 10.1016/j.ydbio.2003.06.003]|
|Ridley AJ. Rho GTPases and cell migrationJ Cell Sci 2001;114:2713–2722. [pmid: 11683406]|
|Schmitz AA,Govek EE,Bottner B,Van Aelst L. Rho GTPases: signaling, migration, and invasionExp Cell Res 2000;261:1–12. [pmid: 11082269] [doi: 10.1006/excr.2000.5049]|
|Wennerberg K,Der CJ. Rho-family GTPases: it's not only Rac and Rho (and I like it)J Cell Sci 2004;117:1301–1312. [pmid: 15020670] [doi: 10.1242/jcs.01118]|
|Lozano E,Betson M,Braga VM. Tumor progression: Small GTPases and loss of cell-cell adhesionBioessays 2003;25:452–463. [pmid: 12717816] [doi: 10.1002/bies.10262]|
|Hall A. Rho GTPases and the Actin CytoskeletonScience 1998;279:509–514. [pmid: 9438836] [doi: 10.1126/science.279.5350.509]|
|Gorvel JP,Chang TC,Boretto J,Azuma T,Chavrier P. Differential properties of D4/LyGDI versus RhoGDI: phosphorylation and rho GTPase selectivityFEBS Lett 1998;422:269–273. [pmid: 9490022] [doi: 10.1016/S0014-5793(98)00020-9]|
|Moissoglu K,Slepchenko BM,Meller N,Horwitz AF,Schwartz MA. In Vivo Dynamics of Rac-Membrane InteractionsMol Biol Cell 2006;17:2770–2779. [pmid: 16597700] [doi: 10.1091/mbc.E06-01-0005]|
|Etienne-Manneville S,Hall A. Rho GTPases in cell biologyNature 2002;420:629–635. [pmid: 12478284] [doi: 10.1038/nature01148]|
|Zhou X,Suto S,Ota T,Tatsuka M. Nuclear translocation of cleaved LyGDI dissociated from Rho and Rac during Trp53-dependent ionizing radiation-induced apoptosis of thymus cells in vitroRadiat Res 2004;162:287–295. [pmid: 15332996] [doi: 10.1667/RR3220]|
|Ota T,Maeda M,Sakita-Suto S,Zhou X,Murakami M,Takegami T,Tatsuka M. RhoGDIbeta lacking the N-terminal regulatory domain suppresses metastasis by promoting anoikis in v-src-transformed cellsClin Exp Metastasis 2006;23:323–334. [pmid: 17111235] [doi: 10.1007/s10585-006-9041-y]|
Previous Document: Insights into female sperm storage from the spermathecal fluid proteome of the honeybee Apis mellife...
Next Document: Activation of calpain-1 in human carotid artery atherosclerotic lesions.