Induced pluripotent stem cells (iPSCs) generated from patient fibroblasts could potentially be used as a source of autologous cells for transplantation in retinal disease. Patient-derived iPSCs, however, would still harbor disease-causing mutations. To generate healthy patient-derived cells, mutations might be repaired with new gene-editing technology based on the bacterial system of clustered regularly interspersed short palindromic repeats (CRISPR)/Cas9, thereby yielding grafts that require no patient immunosuppression. We tested whether CRISPR/Cas9 could be used in patient-specific iPSCs to precisely repair an RPGR point mutation that causes X-linked retinitis pigmentosa (XLRP). Fibroblasts cultured from a skin-punch biopsy of an XLRP patient were transduced to produce iPSCs carrying the patient’s c.3070G > T mutation. The iPSCs were transduced with CRISPR guide RNAs, Cas9 endonuclease, and a donor homology template. Despite the gene’s repetitive and GC-rich sequences, 13% of RPGR gene copies showed mutation correction and conversion to the wild-type allele. This is the first report using CRISPR to correct a pathogenic mutation in iPSCs derived from a patient with photoreceptor degeneration. This important proof-of-concept finding supports the development of personalized iPSC-based transplantation therapies for retinal disease.
Stem cell-derived cell transplantation in the eye is one therapy being explored for inherited retinal degenerations such as retinitis pigmentosa (RP). Recent clinical trials evaluating allogeneic retinal grafts derived from human embryonic stem cells (hESCs) show the procedure to be safe and potentially effective1. However, hESC-based treatments involve the controversial use of human embryos and pose a risk of immune-mediated rejection. Using a patient’s own cells for transplantation would avoid these pitfalls and is possible with induced pluripotent stem cells (iPSCs). Through established protocols2, fibroblasts from a skin biopsy can be returned to a pluripotent state and serve as a renewable, autologous source of replacement cells that avoids the ethical complications of hESCs.
Although the original disease-causing mutation would still be present in patient iPSCs, precise mutation correction is possible through gene editing techniques adapted from the bacterial clustered regularly interspersed short palindromic repeats (CRISPR)/Cas9 system3. The advantage of CRISPR is that its specificity depends largely on a guide RNA (gRNA) that can be readily programmed to target different genomic loci. In this study, we generated iPSCs from a patient with a mutation in the retinitis pigmentosa GTPase regulator (RPGR) gene, which causes an aggressive, X-linked variant of RP (XLRP). We tested whether CRISPR could precisely edit the pathogenic mutation and produce gene-corrected iPSCs for eventual use in autologous transplantation.
All experimental protocols, including informed consent were apporved by the Institutional Review Board approval (AAAF1849) at Columbia University were obtained and all experiments were performed in accordance with relevant approved guidelines and regulations. Informed consent was obtained for all subjects. Autofluorescent imaging and optical coherence tomography were performed as described4. To generate iPSCs, dermal fibroblasts were cultured from the skin biopsy sample and transduced according to previously described protocols5. Pluripotency was demonstrated by teratoma assay conducted in immunodeficient mice (Charles River, Wilmington, MA) and immunocytochemistry staining for pluripotency markers.
CRISPR gRNAs were selected to minimize the off-target profile and to maximize the degree of homology with a target sequence directly centered on the mutation site. Candidates g58 and g59, (G58: GAAGTGGAAGGGGAGGTGGAAGG) and g59 (G59: AAGTGGAAGGGGAGGTGGAAGGG), were each inserted into the gRNA/Cas9 expression vector pBT-U6-Cas9-2A-GFP and transfected into a 293 cell line. Genomic DNA from test cells was amplified by PCR using primers for the RPGR region, and the PCR products were analyzed by the SURVEYOR® assay (Transgenomic, Omaha, NE) for DNA cleavage activity. The expression plasmid containing the g58 sequence and Cas9 were then transfected into the patient-derived C1145-11* iPSC line alongside a single-stranded donor oligonucleotide (ssODN) template. Ten days after transfection, cells were collected for PCR followed by targeted amplicon sequencing to assess for gene correction in the open reading frame-15 (ORF15) region containing the mutation. Deep sequencing templates were obtained by PCR of the genomic sequence, which also detects some non-specific PCR products (not apparent on the gel) due to the very high deep sequencing coverage. These non-specific sequences were categorized under “non-specific/error”. Cells not transfected were used as controls.
We reported previously on the diagnosis of RPGR-associated XLRP in two brothers with significant vision loss6. Fundus examination and imaging showed a bull’s eye lesion with photoreceptor cell death near the fovea (Fig. 1A–D). Whole exome sequencing with Sanger sequencing confirmation uncovered a novel RPGR mutation (c.3070G > T, pGlu1024X) within the ORF15 exon6, a lengthy and repetitive, purine-rich region of the gene that accounts for >60% of all XLRP mutations7. We then cultured fibroblasts from a skin-punch biopsy and transformed them into patient-specific iPSCs. We confirmed that they were capable of differentiating into all three germ layers and expressed the pluripotency markers Oct-4, Sox2, SSEA-4, TRA-1-60, and alkaline phosphatase (Fig. 1E–L). In this state, they can be induced into retinal cells, but a critical limiting factor for transplantation is that they still carry a disease-causing mutation.
Next, we screened 21 gRNAs with high specificity to the region containing the patient’s RPGR mutation (see Supplementary Table). Two candidates were separately inserted into an expression vector also containing the Cas9 endonuclease responsible for mediating target DNA cleavage. A SURVEYOR® assay (Transgenomic, Omaha, NE) showed that one candidate, g58, had relatively high activity for the mutation site (Fig. 2). Because the RPGR sequence is highly repetitive, nonspecific bands were present (see methods). The calculation of cutting efficiency was based on the control band (before nuclease digestion) and the specific bands. The cutting efficiency was approximately 23% for g58. G59 was not active. Thus, g58 was used for gene editing.
Following gRNA validation, we sought to determine whether Cas9-mediated cleavage at the RPGR mutation site could lead to homology-directed gene repair (HDR) in the presence of a co-transfected ssODN. We transfected patient iPSCs with the g58 gRNA/Cas9 expression plasmid and an RPGR anti-sense ssODN. Deep sequencing of transfected cells showed that 13% of reads contained precise correction of the mutation, with replacement of the premature stop codon “TAG” by the wild-type “GAG” codon encoding glutamate at residue 1024 (Fig. 3). Correction of mutation was not seen in any untransfected control iPSCs.
The goal of autologous cell replacement for retinal degenerative disease depends on the ability to correct a patient’s pathogenic mutation before transplantation. Here we have generated patient-specific iPSCs from an XLRP patient and showed that transfection of CRISPR gRNA/Cas9 alongside a donor homology template corrects a point mutation within the RPGR gene ORF15 region, a challenging DNA sequence to manipulate. We believe this is the first report of successful gene correction in human iPSCs associated with inherited retinal degeneration. The present study is significant because it demonstrates that gene editing can be engineered to precisely target a repeat-rich region with high GC content. RPGR spans a 59,000-bp region8 in a human genome containing over 3 billion bases, yet 13% of sequencing reads had correction of a single nucleotide mutation within the repetitive, low-complexity ORF15 region, demonstrating that despite presumed technical hurdles based on the genomic sequence, the RPGR gene is open to CRISPR repair. This rate of repair indicates that CRISPR gene editing may reasonably be part of an autologous transplantation treatment for other photoreceptor degenerations in the future.
The alternative, and currently the more developed, therapeutic modality for genetic retinal disease is gene supplementation therapy. Clinical trials for RPE-associated Leber congenital amaurosis reported in 2008 that gene therapy9 is safe and beneficial for patients. However, recently published three-year follow-up data found that initial gains in retinal sensitivity waned over time and were not accompanied by meaningful improvements in objective measures of visual function10. Moreover, gene therapy in animal models may produce much greater and more sustained rescue in humans at comparable vector doses, suggesting that interspecies genetic differences could limit translation to humans. These and other limits of gene therapy—such as its relative inability to treat dominantly inherited or late-stage disease—might be better addressed through a regenerative gene-corrected iPSC transplantation approach.
The 13% correction rate that we achieved is comparable to other studies of homology-directed CRISPR editing11, and exceeds previous iPSC gene editing studies reporting correction rates closer to 1%12. Such a rate can provide sufficient therapeutic cells, but gene-editing technology is also rapidly improving. The piggyBac transposon is a mobile genetic element that can insert and excise exogenous constructs in a “footprint free” manner for CRISPR in iPSCs11. Minimizing error-prone non-homologous end-joining at DNA cleavage sites through inhibition of DNA ligase IV can also increase the yield of repaired cells13. Definitive analysis of off-targeting rates will be required before eventual clinical use. With repaired patient-specific iPSCs in hand, the next step for iPSCs transplantation therapy is differentiating clonally corrected iPSCs into photoreceptors capable of integrating within the retina. Although a number of challenges remain, significant progress has been made in preclinical transplantation experiments using post-mitotic photoreceptor precursor cells or iPSC-derived en bloc retinal tissue14,15.
Here, we report that patient-derived iPSCs harboring a pathogenic RP mutation are amenable to precise correction by CRISPR/Cas9 gene editing. Our finding represents a concrete first step towards combining CRISPR/Cas9-mediated gene editing with autologous iPSCs to develop a personalized transplantation strategy adaptable to a wide array of retinal diseases.
How to cite this article: Bassuk, A. G. et al. Precision Medicine: Genetic Repair of Retinitis Pigmentosa in Patient-Derived Stem Cells. Sci. Rep. 6, 19969; doi: 10.1038/srep19969 (2016).
This research was supported by the Cure RPGR Fund. VBM is supported by NIH grants [K08EY020530, R01EY024665, R01EY025225, R01EY024698 and R21AG050437], and Doris Duke Charitable Foundation Grant #:2013103, and Research to Prevent Blindness (RPB), New York, NY. The Barbara & Donald Jonas Stem Cell & Regenerative Medicine Laboratory and Bernard & Shirlee Brown Glaucoma Laboratory is supported by NIH core grants 5P30CA013696 and 5P30EY019007, unrestricted funds from RPB, New York, NY, USA. S.H.T. is a member of the RD-CURE Consortium and is supported by Tistou and Charlotte Kerstan Foundation, R01EY018213, New York State C029572, the RPB Physician-Scientist Award, the Foundation Fighting Blindness New York Regional Research Center Grant (C-NY05-0705-0312), the Joel Hoffman Fund, Charles Culpeper Scholarship, Irma T. Hirschl Charitable Trust, Gebroe Family Foundation, and by Foundation Fighting Blindness grant CF-CL-0613-0614-COLU. None of the above listed funding organizations played any role in the design or conduct of the study; data collection, management, analysis, or interpretation; preparation, review, or approval of the manuscript; or the decision to submit the manuscript for publication.