|Exon skipping of hepatic APOB pre-mRNA with splice-switching oligonucleotides reduces LDL cholesterol in vivo.|
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|PMID: 23319054 Owner: NLM Status: MEDLINE|
|Familial hypercholesterolemia (FH) is a genetic disorder characterized by extremely high levels of plasma low-density lipoprotein (LDL), due to defective LDL receptor-apolipoprotein B (APOB) binding. Current therapies such as statins or LDL apheresis for homozygous FH are insufficiently efficacious at lowering LDL cholesterol or are expensive. Treatments that target APOB100, the structural protein of LDL particles, are potential therapies for FH. We have developed a series of APOB-directed splice-switching oligonucleotides (SSOs) that cause the expression of APOB87, a truncated isoform of APOB100. APOB87, like similarly truncated isoforms expressed in patients with a different condition, familial hypobetalipoproteinemia, lowers LDL cholesterol by inhibiting very low-density lipoprotein (VLDL) assembly and increasing LDL clearance. We demonstrate that these "APO-skip " SSOs induce high levels of exon skipping and expression of the APOB87 isoform, but do not substantially inhibit APOB48 expression in cell lines. A single injection of an optimized APO-skip SSO into mice transgenic for human APOB resulted in abundant exon skipping that persists for >6 days. Weekly treatments generated a sustained reduction in LDL cholesterol levels of 34-51% in these mice, superior to pravastatin in a head-to-head comparison. These results validate APO-skip SSOs as a candidate therapy for FH.|
|Petra Disterer; Raya Al-Shawi; Stephan Ellmerich; Simon N Waddington; James S Owen; J Paul Simons; Bernard Khoo|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2013-01-15|
|Title: Molecular therapy : the journal of the American Society of Gene Therapy Volume: 21 ISSN: 1525-0024 ISO Abbreviation: Mol. Ther. Publication Date: 2013 Mar|
|Created Date: 2013-03-01 Completed Date: 2013-10-22 Revised Date: 2014-02-20|
Medline Journal Info:
|Nlm Unique ID: 100890581 Medline TA: Mol Ther Country: United States|
|Languages: eng Pagination: 602-9 Citation Subset: IM|
|APA/MLA Format Download EndNote Download BibTex|
Apolipoproteins B / genetics*, metabolism
Cholesterol, LDL / blood*
Genetic Therapy / methods
Hep G2 Cells
Hyperlipoproteinemia Type II / blood, genetics, therapy
Lipoproteins, VLDL / antagonists & inhibitors, blood
Liver / metabolism
Oligonucleotides / genetics*, metabolism
RNA Precursors / genetics*, metabolism
Receptors, Lipoprotein / genetics, metabolism
Sequence Analysis, RNA
|G0802469//Medical Research Council; G0802469(90972)//Medical Research Council; PG/12/20/29469//British Heart Foundation|
|0/Apolipoproteins B; 0/Cholesterol, LDL; 0/Lipoproteins, VLDL; 0/Oligonucleotides; 0/RNA Precursors; 0/Receptors, Lipoprotein; 0/apolipoprotein B receptor|
Journal ID (nlm-journal-id): 100890581
Journal ID (pubmed-jr-id): 21793
Journal ID (nlm-ta): Mol Ther
Journal ID (iso-abbrev): Mol. Ther.
nihms-submitted publication date: Day: 29 Month: 11 Year: 2012
Electronic publication date: Day: 15 Month: 1 Year: 2013
Print publication date: Month: 3 Year: 2013
pmc-release publication date: Day: 01 Month: 9 Year: 2013
Volume: 21 Issue: 3
First Page: 602 Last Page: 609
PubMed Id: 23319054
|Exon Skipping of Hepatic APOB pre-mRNA with Splice-switching Oligonucleotides Reduces LDL Cholesterol In Vivo|
|Simon N. Waddington5|
|James S Owen1|
|J Paul Simons34|
1Institute for Liver and Digestive Health, Division of Medicine, UCL, London, UK
2Endocrinology, Division of Medicine, UCL, London, UK
3Centre for Biomedical Science, Division of Medicine, UCL, London, UK
4Wolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, Division of Medicine, UCL, London, UK
5Institute for Women’s Health, Division of Medicine, UCL, London, UK, Honorary Reader, School of Pathology, University of the Witwatersrand, Johannesburg, South Africa
|Correspondence: Correspondence should be addressed to B.K. (email@example.com), Dr Bernard Khoo, Division of Medicine (2nd Floor), UCL Medical School, Royal Free Campus, Rowland Hill Street, London NW3 2PF, UK. Tel: + 44 20 77940500 ext 33383
Familial hypercholesterolemia (FH) is a condition characterized by extremely high concentrations of low-density lipoprotein (LDL) cholesterol, most commonly due to genetic defects in the hepatic LDL receptor (LDLR). Patients with the most severe form, homozygous FH, develop life-threatening cardiovascular disease in early adulthood.1 Lowering LDL cholesterol is known to reduce mortality and morbidity, delaying the onset of cardiovascular disease. However, current drug treatments for FH such as statins are insufficiently efficacious and are unable to reduce LDL cholesterol and the risks of cardiovascular disease to baseline. Another therapy in use is LDL apheresis which is highly effective at reducing cholesterol levels, but is expensive and requires patients to attend specialist centres for treatment every 1-2 weeks.2 Alternative therapies to lower LDL cholesterol are needed.
Apolipoprotein B (APOB) has emerged as a key target for LDL cholesterol-lowering therapies. Two natural protein isoforms are generated from the APOB gene, APOB100 and APOB48. The principal structural apolipoprotein in LDL particles is the full-length APOB100 isoform. APOB100 is expressed in the liver and assembled into very low-density lipoprotein (VLDL) particles. These are catabolised to form LDL particles, which are normally recycled via the liver when APOB100 binds to the LDLR. Disruption of this interaction, e.g. due to mutations in LDLR or APOB100, cause accumulation of LDL particles in the circulation and hypercholesterolemia, ultimately leading to atherosclerosis and cardiovascular disease. APOB48 is generated by cell-specific RNA editing of a CAA codon to a premature UAA termination codon in intestinal enterocytes, and is identical to the N-terminal 48% of APOB100 (Figure 1). APOB48 is not assembled into VLDL particles but instead into chylomicrons, whose function is to transport dietary fat and fat-soluble vitamins from the intestine. Disruption of intestinal APOB48 expression and chylomicron assembly is characterised by fat intolerance and malabsorption of fat and fat-soluble vitamins such as Vitamins A, D, E and K.3, 4 Ideally any treatment aimed at reducing LDL cholesterol by interfering with APOB should be selective for APOB100, and should have no effect on APOB48.
In contrast to familial hypercholesterolemia, the antithetical phenotype of familial hypobetalipoproteinemia results from expression of mutant, C-terminally truncated APOB isoforms and is characterised by very low LDL cholesterol, protection from cardiovascular disease, and increased longevity. These shortened APOB100 isoforms reduce VLDL assembly and secretion, and increase LDL clearance from the bloodstream, leading to profoundly low LDL cholesterol levels typically <1.8 mmol/L, protection from atherosclerosis and a longer lifespan.5,6 In order to mimic hypobetalipoproteinemia for therapy, we have developed ‘APO-skip’ splice-switching oligonucleotides (SSOs) that induce the skipping of APOB exon 27 to generate a truncated APOB isoform, APOB87.7
Here, we show that sequence optimization of our previously published SSOs7 is able to increase the in vitro exon skipping efficiency of APO-skip SSOs by up to 15-fold. We confirm that treatment induced expression of the truncated isoform APOB87, and that this did not affect APOB48 production. In mice transgenic for human APOB, intravenous injection of APO-skip SSOs resulted in exon 27 skipping which persisted for at least 6 days after a single dose. Weekly administration resulted in reduced LDL cholesterol compared to controls.
In the treatment of Duchenne Muscular Dystrophy with SSOs, targeting sequences within the exon is more effective than targeting splice sites.8 However, this strategy was not notably successful for inducing skipping of exon 27 in the APOB gene (Supplementary Figure S1). As previously demonstrated, SSOs can induce significantly more skipping of APOB exon 27 when directed against branch point binding sites, the polypyrimidine tract and the 3′ splice site of APOB exon 27.7
Therefore, starting with the most effective previously published oligonucleotide skip27-3B, herein designated SSO 1, we systematically optimized the SSO sequence and backbone modifications to increase efficiency. All SSOs were 2′-O-methyl RNA oligonucleotides unless otherwise stated.
For accurate quantification of the full-length (APOB100) and skipped (APOB87) mRNAs, we developed two reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) assays specific for the APOB26-27 and APOB26-28 exon-exon junctions. As recommended by Vandenbroucke et al.9, each assay used a single standard curve generated from a plasmid containing both the APOB26-27 and APOB26-28 PCR products. The plasmid was serially diluted resulting in a 7 point standard curve of 107-101 copies per reaction under the assay conditions. The use of a single common standard curve in both assays ensures direct proportionality of the RT-qPCR copy number values and allows calculation of skipping efficiency as a ratio within each sample without the need for reference genes for normalization.
We selected the human hepatocellular carcinoma cell line HepG2 as our model system because these cells express APOB100 and have been shown to support exon skipping and production of the APOB87 isoform.7 Cells were transfected with the various SSOs as described in the methods and exon skipping efficiency was analysed 48 h later using the RT-qPCR assays described above. As shown in Figure 2, the prototype SSO 1 targets the 3′ splice site (splice acceptor) and two potential branch point sites in intron 26-27. The newly developed RT-qPCR assay demonstrated that SSO 1 has a relatively low skipping efficiency of 4.14% in comparison to its scrambled control, SSO sc1, or mock-transfected control (Figure 2). Attempts to reduce the SSO length or further illuminate the essential target sequences resulted in severe reductions in skipping efficiency in all cases (Figure 2 - SSOs 3-13, 17-21). Addition of the intron 27-28 5′ splice site (splice donor) to the target sequence led to a significant increase in efficiency (SSO 14: 14.17%), while modification of the 5′ end with fluorescein (SSO 1-F) or biotin (SSO 1-B) also increased the skipping efficiency compared with the parental SSO 1 (Figure 2). Similarly, the SSO 14 sequence modified with 5′ fluorescein (SSO 14-F) and biotin (SSO 14-B) showed increased skipping efficiency in comparison to SSO 14. However, the largest rise in skipping efficiency occurred when the backbone of SSO 14 was modified with 5 phosphorothioate modifications (PS) on the 5′ and 3′ ends (SSO 14-53P: 58.73%). In comparison to the respective non-PS modified SSOs, full PS modification of SSO 14 (SSO 14-P) resulted in reduced efficiency, while full PS modification of SSO 1 (SSO 1-P) resulted in increased efficiency. Additional 5′ fluorescein modification on fully PS modified SSOs did not lead to further improvement in skipping levels for either the SSO 1 (SSO 1-PF) or the SSO 14 (SSO 14-PF) sequence.
As previously reported, the exon 27-skipped APOB mRNA isoform escapes nonsense mediated decay and is translated into a secreted protein, APOB87, in HepG2 cells.7 Here, we confirm this finding in cultured Caco-2 cells, a human epithelial colorectal adenocarcinoma line, which after reaching confluence differentiate to resemble enterocytes of the small intestine.10 These cells have been used as a model for lipoprotein synthesis in the intestine and, in addition to APOB100 synthesis, express both the APOB100 and APOB48 protein isoforms once cell confluence and differentiation is achieved.11, 12 As with HepG2 cells, secretion of apolipoproteins can be stimulated by incubation with oleic acid.13 However, achieving efficient transfection on differentiated, fully confluent cells proved impossible, so we reverse transfected near-confluent Caco-2 cells, plated at high density, and incubated for 72 h before collection of supernatant for Western blotting and extraction of cellular RNA. Differential toxic effects of transfection resulted in different cell densities, in turn leading to inconsistent differentiation and consequent variation in the levels of APOB expression. Nevertheless, as shown in Figure 3a, transfection with each functional SSO (14, 1-F, 14-F, 14-53P and 14-53PF) clearly resulted in expression of the intended APOB87 isoform, while transfection with control scrambled SSOs sc14-53P and sc14-53PF did not. Mock-transfected cells also did not express the APOB87 isoform.
The APOB48 isoform is clearly visible in the blots of cells treated with SSO 14, 1-F and 14-F showing that transfection with these oligonucleotides, and the resulting exon skipping, does not substantially inhibit APOB48 expression. The greater non-specific toxicity resulting from Lipofectamine 2000 transfection of the longer PS modified SSOs resulted in a lower cell density and lower level expression of both APOB100 and APOB48 by Caco-2 cells treated with SSOs 14-53P and 14-53PF, sc14-53P and sc14-53PF (Figure 3a). Despite this, the data show that APOB48 expression was not substantially diminished, relative to APOB100, in the cells treated with functional SSOs 14-53P and 14-53PF when compared with their respective negative controls, sc14-53P and sc14-53PF.
Similar Western blotting and skipping efficiency data are shown for HepG2 cells (Figure 3b). As expected, APOB48 was not expressed in these cells, but treatment with the functional SSOs 1, 14 and 14-F also resulted in the expression of the APOB87 isoform, whereas non-functional, scrambled control SSO sc1 and mock-transfected cells showed only the APOB100 isoform. The respective skipping efficiencies are given below each blot and clearly demonstrate that as little as 3% skipping results in detectable APOB87, while skipping levels of more than 10% lead to substantial expression and secretion of this isoform (Figure 3a,b).
Having shown that our best SSO candidates cause up to 60% skipping in HepG2 and Caco-2 cells, we proceeded to evaluate the skipping efficiency of selected SSOs in transgenic mice expressing human APOB.14 We chose to use SSO 14-53PF for these studies because it is a fluorescently labelled version of SSO 14-53P and thus allowed tracking of SSO delivery to the liver using fluorescence microscopy.
A standard IV injection of naked SSO 14-53PF (25 mg/kg) via the tail-vein resulted in minimal delivery and skipping efficiencies not significantly above background, with little improvement seen with hydrodynamic injection (Supplementary Figure S2). Examination of tissues and urine with fluorescence microscopy showed that SSO 14-53PF was cleared rapidly in the urine (data not shown). This is likely to be due to the length of the SSO and the relatively small number of PS modifications used, leading to insufficient serum protein binding. In order to achieve efficient hepatic uptake, a cationic complexing reagent, Invivofectamine 2.0 (IVF2.0), was used which allowed efficient delivery to all hepatocytes at both 12.5 and 25 mg/kg doses (Supplementary Figure S2).
Measuring skipping efficiencies after IVF2.0 delivery (Figure 4a), the lower dose of 12.5 mg/kg resulted in relatively low efficiency 24 h after injection (~6%). Doubling the dose to 25 mg/kg increased skipping efficiency by nearly 5-fold (~29%), although the highest dose of 50 mg/kg did not provide further increases. As expected, control mice injected with vehicle only showed background level skipping. To investigate the hepatotoxicity of the treatment, we measured AST and ALT levels. The vehicle only controls (IVF2.0 without SSO) showed a massive increase of AST (>3500 U/L) and ALT (>2800 U/L) levels over baseline (95 ± 23 U/L, n=11 and 62 ± 17 U/L, n=11; respectively). Similarly large increases of AST and ALT levels were observed with the 50 mg/kg dose, but encouragingly for the 25 mg/kg group the increases were smaller (AST 959 ± 433 U/L, ALT 511 ± 316 U/L, n=5) and for the 12.5mg/kg group were close to baseline values (AST 134 ± 35 U/L, ALT 60 ± 13 U/L, n=3).
Based on these results we selected the 25 mg/kg dose as the best combination of high efficiency and acceptable liver toxicity. We then investigated the persistence of the effects of SSO treatment. After injection of a 25 mg/kg dose, exon skipping levels were highest after 24 h (29%), dropped by only a third within 72 h, and after 144 h (6 days) exon skipping levels still remained above 5% (Figure 4b).
To allow for the possibility that in vivo exon skipping efficiencies are only partly predictive of the results of in vitro experiments, we compared several SSOs from our in vitro screen by measuring exon skipping 6 days after a single injection with SSO. As shown in Figure 4c, only SSOs 14-53P and 14-53PF demonstrated efficacy at this time point with no significant difference in efficiency between them. We performed relative quantification of splice variant expression levels between successful treatment (SSO 14-53P and 14-53PF) and control/unsuccessful treatment (SSO sc14-53PF/1-F and 14-F). Murine B2M and ACTB were used as reference genes after geNORM analysis established these as the two most stable (V2/3=0.103).15 Calculation with the REST software16 demonstrated significant 10-fold up-regulation of the exon 27 skipped isoform (huAPOB26-28 assay; p=0.001) whereas the expression levels of the exon 27 included isoform (huAPOB26-27), total human APOB (huAPOB25-26) and murine APOB did not change (Figure 4d).
Having determined that exon skipping persists for at least 6 days after a single dose, we investigated whether 8 weekly treatments would change the plasma lipid profile. To reduce toxicity, we elected to decrease the dose slightly from 25 mg/kg to 20 mg/kg. This proved successful, as no significant differences in AST or ALT levels were found when comparing treatment groups (SSO 14-53P, SSO sc14-53P and Pravastatin) with the untreated control group. With the functional SSO 14-53P this regimen resulted in a modest 6.76% skipping efficiency when sampled 72 h after the last injection (Figure 5a). As anticipated, skipping levels after treatment with control SSO sc14-53P or 0.25 mg/ml Pravastatin in drinking water did not differ from levels in the untreated control group.
Relative quantification of treatment with SSO 14-53P versus the control SSO sc14-53P using murine GAPDH, HPRT, SDHA, B2M and ACTB as reference genes (geNORM V4/5=0.007) showed statistically significant 18-fold up-regulation of the exon 27 skipped isoform (p=0.001). The expression levels of the exon 27 included isoform, total human APOB and murine APOB did not differ between SSO 14-53P and control treatments (Figure 5b).
To assess the effects of SSO treatments on lipid concentrations, we measured LDL cholesterol in serum before commencing treatment and after 3, 6 and 8 weekly doses of SSO/IVF2.0 complex. The lipid analysis was complicated by a confounding non-specific effect of IVF2.0, which results in an increase in measured LDL cholesterol (Supplementary Figure S3). Nevertheless, by baseline-correcting the delta LDL values achieved during treatment (SSO 14-53P and Pravastatin) with their respective control values (delta LDL of SSO sc14-53P and no treatment, respectively) we show that APO-skip treatment with SSO 14-53P resulted in a 51% relative reduction after three injections and a sustained 34% relative reduction over the rest of the test period (Figure 5c). In contrast, treatment with Pravastatin decreased LDL cholesterol by 8-12% over time.
The potential therapeutic use of SSOs to modify splicing was first described in 1993, to correct aberrant processing of mutant beta-globin pre-mRNAs,17 but has been developed furthest for treatment of Duchenne muscular dystrophy (DMD) where promising data from a Phase 2 study have been published recently.18 For exon skipping in DMD, SSOs targeting exonic sequences such as exonic splice enhancers (ESEs) have been more efficient than SSOs targeting donor and acceptor sites in the flanking introns.8 In the case of APOB exon 27, the converse appears to be true, as to date a number of SSOs targeting exon sequences, some of them designed according to guidelines published by Aartsma-Rus,19 have shown little activity (Khoo et al.7 and Supplementary Figure S1). This may reflect the lack of alternative splicing of APOB and/or the extraordinary length of APOB exon 26; notably, the first half of exon 27 contains curiously few matches for ESEs and many for splicing silencer motifs according to Human Splicing Finder.20
RNA structure modelling of the exon 27 sequence plus 50 nucleotides from the flanking introns with mfold21 and RNAstructure22 suggests that the 3′ end of intron 26-27 remains single stranded, allowing effective binding of 3′ spliceosome components. The beginning of exon 27 shows a high probability of a short stem-loop structure with the actual splice site situated at the apex of the loop followed by a 10 nucleotide unstructured region and a more complex stem-loop presenting a SRp55 ESE motif. The 3′ half of exon 27 largely is predicted to form double-stranded structures with the beginning of intron 27-28, but again displaying the 5′ splice site in a short loop. Bimolecular RNA folding with various SSOs suggests that the exon-internal SSOs do not change the single-stranded nature of the intron 26-27 3′ end, the 3′ splice site loop or the double stranded exon 27/intron 27-28 region. Although the SRp55 ESE motif can be masked with exonic SSOs, this is clearly not sufficient for effective exon skipping. In contrast, SSO 1 is predicted to sequester the 3′ end of intron 26-27 into a double strand, forcing the 3′ splice site loop to move along into the exon 27 sequence closer to the SRp55 ESE. Thus, the actual 3′ splice site is hidden while SRp55 binding may be inhibited by the proximity of the 3′ loop. Still, the double-stranded nature of exon 27/intron 27-28 border region remains unchanged. Only when this border region is modified to a more open single-stranded formation and the 5′ splice site is blocked in addition, as is predicted to be the case with SSO 14-53P, could we achieve significantly higher exon skipping efficiencies.
We found that two types of modification appear to increase SSO exon-skipping efficiency. Firstly, partial PS modification increased exon-skipping, whereas full PS modification seemed to reduce this somewhat. PS modification increases oligonucleotide stability to nucleases23 but reduces binding affinity to RNA. This can be overcome using a ‘mixed-backbone’ strategy as applied here with the partial PS modification to the 5′ and 3′ ends of our SSOs.24 Secondly, SSOs bearing 5′ fluorescein or biotin compared to non-modified SSOs of the same sequence were more efficient at exon-skipping. This observation has not been reported before for other exons. A possible explanation for this phenomenon might be that the 5′ fluorescein group is more hydrophobic and enables charged SSO translocation across the membrane, although this cannot explain the effectiveness of 5′ biotinylation, as biotin is a relatively polar moiety. A more unifying explanation for our observations is that the presence of these groups near the 5′ splice site of exon 27 interferes with recognition of this splice site, consistent with our structural view of APOB exon 27 skipping. Although early attempts to reduce the length of the resulting 50-mer SSO led to severe efficiency losses, our more recent experiments which take RNA structure modelling into account suggest that exon skipping efficiencies comparable to 14-53P can be achieved with much shorter SSOs (unpublished). These shorter SSOs, together with more extensive PS modification, should also lead to more efficient hepatocyte delivery when given ‘naked’ without the requirement for a delivery reagent. However, the extent of PS modifications must be balanced against the propensity of these polyanionic modifications to trigger non-specific effects by binding to other plasma proteins.24
However achieved, the down-regulation of APOB100 expression is a validated means of reducing LDL cholesterol. This is particularly important in homozygous FH patients who present with extremely high LDL cholesterol levels, resulting in premature CVD morbidity and mortality in late childhood or early adulthood.25 Unfortunately, aggressive treatment with potent statins achieves only around 25% decline in LDL in this population since statins mainly work through upregulation of LDLR in the liver, which is non-functional in FH patients. Nevertheless, even small LDL cholesterol reductions that do not come close to achieving normal levels are directly related to significant survival benefits, and further decreases are likely to accrue even more benefits.25 Our in vivo data demonstrate that APO-skip SSOs resulted in a sustained 34-51% drop in LDL levels in human transgenic APOB mice, compared to control SSOs. This large reduction was associated with a relatively low exon skipping efficiency of 6.8%. This seemingly paradoxical finding may be explained by the similarity of APOB87 to truncated human APOB100 isoforms such as APOB89 and APOB87-Padova. In subjects expressing these truncated isoforms, cholesterol levels are well below normal, typically <1.7 mmol/L,26-28 due to greater catabolic rates of particles containing the shortened APOB isoforms29. Aguilar-Salinas et al.30 also report that production rates of VLDL-APOB100 and LDL-APOB100 particles in truncated APOB heterozygotes were ~30% of normal, suggesting a dominant negative effect. Thus, even low levels of exon skipping will likely be enough for significant therapeutic effects, suggesting that lower doses of APO-skip treatment will achieve clinically relevant effects compared to other oligonucleotide-based therapies in development.
Current approaches to the reduction of APOB100 expression include antisense gap-mer oligonucleotides such as mipomersen,31 locked nucleic acid oligonucleotides developed by Santaris,32 and RNA interference variants such as an AAV-delivered shRNA33 or liposome-packed siRNA.34 None of these approaches is selective for APOB100, and each could potentially cause down-regulation of all APOB expression, including the APOB48 isoform necessary for fat and fat-soluble vitamin absorption. It is claimed that this is not an issue due to tissue tropism33 or the natural distribution to liver when SSO is injected subcutaneously.35 However, a study in mice, using the mouse equivalent of mipomersen, showed a 54% down-regulation of intestinal APOB100 mRNA, although curiously APOB48 protein levels appeared unchanged.36
A conceivable future oral formulation of SSO or siRNA to replace subcutaneous injections would certainly bring the SSO or siRNA in contact with intestinal cells. Down-regulation of APOB48 in the intestine would thus expose patients to the side-effect of fat and fat-soluble vitamin malabsorption. In contrast, our approach does not interfere with APOB48 expression, thus avoiding these potential side effects. This is consistent with the fact that normal APOB48 expression is found in subjects with familial hypobetalipoproteinemia expressing a truncated APOB89 isoform.37
In summary, APO-skip SSOs are able to reduce LDL cholesterol significantly even at relatively low exon skipping efficiencies and offer advantages over other therapies in current development. At the present early stage the SSO designs presented here are not practical therapies due to the length of the SSO and requirement for vehicle. To translate the APO-skip concept to the bedside, we anticipate that shortening the SSOs with sequence optimization and consideration of other oligonucleotide chemistries will eventually enable hepatic delivery without vehicle and with reduced manufacturing costs; our designs offer a basis from which to develop these newer-generation APO-skip SSOs.
HepG2 (85011430) and Caco-2 (86010202) cells were acquired from the European Collection of Cell Cultures (Salisbury, UK) and used for no more than 25 passages. Cell culture media, FBS, GlutaMAX, non-essential amino acids, Lipofectamine 2000, Opti-MEM, pCR2.1, Invivofectamine 2.0 and all Western blotting reagents were obtained from Life Technologies (Paisley, UK); phosphate-buffered saline (PBS) from the Royal Free Hospital Pharmacy; insulin (Actrapid®) from Novo Nordisk (Crawley, UK); and all other reagents from Sigma Aldrich (Gillingham, UK) except where stated. All reagents, machines and consumables for RNA extraction and RT-qPCR were from Qiagen (Crawley, UK) unless otherwise noted. Splice-switching oligoribonucleotides and DNA primers were purchased from Eurogentec (Fawley, UK) or Integrated DNA Technologies (Coralville, IA, USA) and their sequences can be found in Figure 2, Supplementary Figure S1 and Supplementary Table S1. Human APOB100 transgenic mice14 (B6.SJL-Tg(APOB)1102Sgy N20+?) were obtained from Taconic (Germantown, NY, USA) and given standard chow and water ad libitum. All studies were approved by the UK Home Office under the Animals Scientific Procedures Act 1986. Mice were intravenously injected via the tail vein and killed by cervical dislocation.
These methods have been described in detail in Disterer and Khoo,38 but may also be found in the supplementary methods. MIQE guideline39 compliant data are available in Supplementary Tables S1, S2 and Supplementary Figure S4.
Caco-2 cells were seeded at 1×107 cells in 10 cm plates and transfected as described above. For protein extraction, plates were washed three times with PBS containing Complete Protease Inhibitor Cocktail tablets (Roche, Burgess Hill, UK) and then incubated with 5 ml Opti-MEM I containing 100 μg per ml oleic acid/BSA for 4 hours to encourage APOB synthesis and secretion. The supernatant was collected and stored at −80 °C. The supernatants were concentrated 10-fold using Vivaspin 2 columns with polyethersulfone membranes and a molecular weight cut-off of 30,000 Da (Sartorius Stedim, Binbrook, UK). Protein concentration was determined using a Novagen BCA kit from Merck (Feltham, UK) as per the provided instructions. The appropriate amount of total protein (20-25 μg) in water containing 1x NuPAGE LDS sample buffer and reducing agent was denatured at 70 °C for 10 min and then loaded onto a NuPAGE Novex 3-8% Tris-Acetate mini gel together with HiMark pre-stained protein standard and human APOB protein (ab77903, Abcam, Cambridge, UK). Gels were run in NuPAGE Tris-Acetate SDS running buffer containing 1x NuPAGE Antioxidant at a constant 150 V for 90-120 min. Proteins were transferred from the gel to a Immobilon-P PVDF membrane (Millipore, Watford, UK) in ice-cold CAPS buffer [pH 11.0] containing 10% ethanol, 0.01% SDS and 1x NuPAGE Antioxidant with an electric potential of 55 V for 10 min and 30 V for 1 h. Membranes were blocked overnight in 5% non-fat milk and 0.1% Tween-20 and then incubated with a polyclonal goat anti-human APOB antibody (ab742, Millipore) at a 1:3000 dilution for 1 h at RT. The membrane was then stained with anti-goat IgG-HRP (A5420, Sigma Aldrich) secondary antibody at a 1:10,000 dilution for 1 h at RT. Protein bands were visualised with the ECL western blot detection kit and ECL Hyperfilm (GE Healthcare, Chalfont St Giles, UK).
SSOs were complexed with Invivofectamine 2.0 (IVF2.0) for liver-specific delivery in vivo. SSOs at a concentration of 3 mg/ml were diluted with complexation buffer supplied with IVF2.0 to achieve 1.5 mg/ml. This was then added directly to an equal volume of IVF2.0 in 50 ml tubes to obtain a 1 ml IVF2.0 to 1.5 mg SSO ratio and immediately vortexed. This solution was then incubated at 50 °C under constant rotation for 30 min. After incubation 14-17 volumes of PBS were added and 12 ml of this was transferred into a pre-washed Amicon Ultra-15 Centrifugal Devices with Ultracel-50 membrane (Millipore). The Amicon filter was centrifuged at 1600 × g until the volume was reduced to <1 ml and another 12 ml of the diluted IVF2.0/SSO complexation solution were added. The process was repeated until the whole volume was concentrated to 2-4 mg/ml, as appropriate to achieve the required dose in 150-200 μl of injection volume.
For cholesterol profiles mice were fasted for 2 hours before blood collection. Blood was collected in microcentrifuge tubes and allowed to clot at room temperature for at least 2 h or at 4°C overnight (consistent within experiment). Samples were spun at 9500 × g at 4°C for 10 min and then the supernatant was carefully transferred to fresh tubes to avoid carry-over of erythrocytes. This step was repeated with the supernatant samples. Sera were aliquoted and stored at −80°C. For analysis, aliquots were sent to the MRC Mary Lyon Centre (Harwell, UK). Samples were diluted 1:3 and analysed on Olympus AU400 Clinical Chemistry platform assays.
Data analysis was performed using GraphPad Prism 5 (San Diego, CA). Values in text and figures reflect the mean ± standard deviation (S.D.) unless otherwise stated. Statistical significance was determined with one-tailed unpaired t-test when comparing 2 groups only or else with ANOVA using the Bonferroni post-hoc test.
FN1The authors declare no other conflict of interest.
The authors thank Xavier de Mollerat du Jeu (Life Technologies) for technical advice with IVF2.0 and Tertius Hough (MRC Mary Lyon Centre, Harwell, UK) for performing the serum analyses. This work was supported by the MRC Developmental Pathway Funding Scheme (G0802469) and by UCL Business. BK, JSO, JPS and PD are inventors of an associated patent.
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Keywords: apolipoprotein B, exon skipping, familial hypercholesterolemia, oligoribonucleotides, quantitative reverse-transcription polymerase chain reaction, splice-switching oligonucleotides.
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