In vivo delivery is a major barrier to the use of molecular tools for gene modification. Here we demonstrate site-specific gene editing of human cells in vivo in hematopoietic stem cell-engrafted NOD.Cg-PrkdcscidIL2rγtm1Wjl (abbreviated NOD-scid IL2rγnull) mice, using biodegradable nanoparticles loaded with triplex-forming peptide nucleic acids (PNAs) and single-stranded donor DNA molecules. In vitro screening showed greater efficacy of nanoparticles containing PNAs/DNAs together over PNA-alone or DNA-alone. Intravenous injection of particles containing PNAs/DNAs produced modification of the human CCR5 gene in hematolymphoid cells in the mice, with modification confirmed at the genomic DNA, mRNA and functional levels. Deep sequencing revealed in vivo modification of the CCR5 gene at frequencies of 0.43% in hematopoietic cells in the spleen and 0.05% in the bone marrow: off-target modification in the partially homologous CCR2 gene was two orders of magnitude lower. We also induced specific modification in the β-globin gene using nanoparticles carrying β-globin-targeted PNAs/DNAs, demonstrating this method’s versatility. In vivo testing in an enhanced green fluorescent protein-β-globin reporter mouse showed greater activity of nanoparticles containing PNAs/DNAs together over DNA only. Direct in vivo gene modification, such as we demonstrate here, would allow for gene therapy in systemic diseases or in cells that cannot be manipulated ex vivo.
While viral vectors or plasmid delivery vehicles have been used for many gene therapy applications in vivo, the clinical use of these methods has been limited partially because of the nonspecific nature of gene editing and delivery: delivered genes are integrated into random sites, or expressed in plasmids where they are not under their normal regulation. In contrast, site-specific editing of genes at their endogenous loci could be used to treat monogenic disorders or introduce advantageous genomic changes. Genes edited in this manner remain under their normal regulatory control, unlike genes delivered via plasmids or inserted as cDNA constructs into other genomic loci. Site-specific editing by homologous recombination does not pose the dangers of nonspecific integration inherent to gene therapy dependent on delivery by viral vectors.1 Despite these advantages, efficient non-toxic intracellular delivery remains a barrier to the clinical use of triplex-forming oligonucleotides, small fragment homologous recombination, transcription activator-like effector nucleases (TALENs) and zinc-finger nucleases (ZFNs), although several delivery strategies have been developed for these systems, ranging from microinjection to direct addition of reagents to cells. The most commonly used methods are standard nucleofection or electroporation, which leads to cell death when applied ex vivo,2, 3, 4 and cannot be readily applied in vivo. Direct in vivo gene editing would eliminate the expense and risk of cell harvests, opening the doors for gene therapy in cells that cannot be manipulated outside the body.
Previous studies have demonstrated site-specific editing of the mouse genome or reporter genes in vivo,5, 6, 7 ex vivo editing of human cells followed by transplant into murine models3, 8 or in vivo knock-in of cDNA fragments.9 Small fragment homologous recombination has been used for site-specific editing of the human globin and cystic fibrosis transmembrane receptor genes,10, 11 and TALENs have been successfully used for targeted mutagenesis in several model systems. ZFNs represent a promising technology for site-specific gene editing, with clinical trials in progress for use of this technology in the treatment of HIV-1 infection. ZFNs have been used for both ex vivo editing of CCR5 in hematopoietic cells and subsequent transplant into mouse models conferring HIV-1 resistance,3 and insertion of whole cDNA fragments in vivo in mice with high efficiency using viral vectors.9 However, none of the current technologies for site-specific gene editing have been used directly to edit human genes in human cells in vivo. Our study is unique in its combination of two technologies—synthetic triplex-forming oligonucleotides and polymer nanoparticles—to modify human cells after systemic delivery into chimeric mice.
Triplex-forming peptide nucleic acids (PNAs) are an effective chemical tool that can mediate the recombination of donor DNA fragments with genomic DNA to introduce gene modifications.12 These PNA molecules form a PNA–DNA–PNA triplex that provokes the cell’s own DNA repair machinery12, 13 and thereby stimulates recombination with donor DNAs to cause heritable changes in targeted genes. Mechanisms of DNA repair and recombination induced by triplex structures have been reviewed previously.14, 15 Current evidence suggests that nucleotide excision repair has a role in recognizing and repairing triplex-induced DNA helical alterations12, 13, 16, 17 and that triplex structures are recognized by the xeroderma pigmentosum group A (XPA) and replication protein A (RPA) repair factors.17 However, further work is needed to fully elucidate the mechanism of PNA triplex promotion of homologous recombination events. In earlier work, we developed PNA/DNA combinations that modify the human CCR5 gene, leading to the production of HIV-resistant cells,8 along with PNA/DNA molecules to correct the human β-globin gene at the location of a common thalassemia splice-site mutation.13 In both of these systems, co-delivery of the PNAs and DNAs led to much higher levels of genome modification than delivery of DNAs alone. However, delivery of PNAs remains a challenge. Previous studies have shown that systemic administration of naked triplex-forming PNAs led to minimal levels of mutagenesis above background in a mouse reporter system.7 Novel delivery techniques, such as conjugation with cell penetrating peptides7 or use of new delivery vehicles, such as we report here, will be needed to improve the in vivo activity of triplex-forming PNAs.
We have previously engineered poly(lactic-co-glycolic acid) (PLGA), an FDA-approved biocompatible material, to produce nanoparticles that deliver nucleic acid cargo.18, 19 Most recently, we showed that PLGA nanoparticles carrying PNA/DNA can introduce site-specific genomic modifications in human hematopoietic stem and progenitor cells (HSPCs) in vitro, with higher efficiency and lower toxicity than nucleofection.2 In this recent study, we found that particles containing both PNAs and DNAs were more effective than particles with DNAs alone, or than a combination of particles separately containing the two molecules. We report here that this technology can also produce in vivo gene editing in human hematopoietic cells, which was demonstrated by intravenous injection of PNA/DNA-containing nanoparticles in a humanized mouse model that is relevant to clinical medicine.
PLGA nanoparticles encapsulating PNAs/DNAs for the introduction of modifications in the CCR5 gene were formulated using a double-emulsion solvent evaporation technique, yielding particles approximately 150 nm in diameter (Figure 1a). Two donor DNA molecules were used (donor 1 and donor 2), each capable of introducing a different 6 bp modification that inserts an in-frame stop codon into the CCR5 gene. Nanoparticles coated with a cell-penetrating peptide derived from HIV-1 transactivating protein (TAT) or from the Drosophila antennapedia peptide (AP) were also produced, using a surface-modification approach that has been described previously.20
Both unmodified (CD) and DSPE-polyethylene glycol (PEG) (DP) surface-modified particles were formulated and tested. Addition of DSPE-PEG to nanoparticles in the aqueous phase of the second emulsion results in partitioning of the DSPE phospholipid in the polymer, with PEG being displaced on the surface of the nanoparticle along with any moiety attached to the PEG,20 such as TAT or AP. This surface modification technique was chosen because of previous success in using DSPE-PEG-modified particles to deliver small interfering RNA to a cell line reporter and tumor xenografts.20 Loading of nucleic acids in nanoparticles (Figure 1b) and nucleic acid release over 48 h (Figure 1c) was determined for all particle types, showing efficient loading and release of nucleic acids. The biodegradation of PLGA polymer has been extensively studied in the past: hydrolysis of the polymer follows first-order kinetics, with degradation occurring over the span of weeks, with initial PLGA molecular weight and pH of the incubating media both affecting the duration of breakdown.21 In addition, to show degradability of our particles, we examined the loss of the PLGA nanoparticles over 10 days when incubated at 37 °C, and found approximately 50% loss of material over 10 days (Supplementary Figure 1).
In vitro nanoparticle screening was performed to determine which particles to use in in vivo studies. Consistent with our previous studies,22 we found that combined PNA/DNA nanoparticles had greater in vitro activity than DNA-alone nanoparticles (Figure 2a). In addition, we found that PNAs and DNAs released from the particles during controlled release could be nucleofected into cells and still mediate modification, showing that released PNAs/DNAs are still active. Finally, released nucleic acid simply added to the cells did not lead to levels of modification as high as with nanoparticle delivery or nucleofection, confirming that the delivery step is key. As we have observed before, PNA/DNA nanoparticles were more effective than introduction of PNAs/DNAs by nucleofection. Cell survival was also greater with nanoparticle addition than with nucleofection, consistent with our previous studies.22 DSPE-PEG, DSPE-PEG-TAT and DSPE-PEG-AP nanoparticles carrying the donor DNAs alone were compared with unmodified nanoparticles (equivalent nucleic acid doses). In CD34+ HSPCs, both AP- and TAT-modified particles were found to be slightly more active (Figure 2b). Our results with TAT were most consistent and thus TAT-modified particles were tested in subsequent experiments in animals. In addition, TAT has been shown to increase uptake of payloads to HSPCs.23
NOD-scid IL2rγnull mice exhibit complete reconstitution of the hematopoietic system after transplantation of human CD34+ cells into newborns, with a significant presence of human cells in peripheral blood, bone marrow, spleen, lung, liver, thymus and small intestine.3 Our basic experimental design using this mouse model is outlined in Figure 2c. Untreated wild-type human CD34+ HSPCs were injected into NOD-scid IL2rγnull neonatal mice and reconstitution of the hematolymphoid system was confirmed 12 weeks post-transplant to be at normal levels (Figure 3a). PNA/DNA-containing nanoparticles or naked PNAs/DNAs were then injected via the tail vein. At 10 days post-treatment, mice were killed and analyzed for the presence of the targeted modifications in whole organs and sorted cells.
We previously developed an allele-specific polymerase chain reaction (AS-PCR) to reliably detect CCR5 modifications at the DNA level: detection of gene modification by AS-PCR corresponded well to mRNA and protein expression of the modified gene.8 A different primer set can be used to detect separately each of the two introduced modifications. Quantitative AS-PCR (qAS-PCR) can be used to determine the relative levels of gene modification between treatment groups, and relative gene modification can be calculated using the 2−ΔΔCt method.24 As controls, non-reconstituted mice (which lack human cells) treated with CCR5-targeted nanoparticles did not exhibit detectable gene modification, consistent with the absence of the target sequence in the mouse genome (Figure 3b), confirming that any gene modifications observed are in the CCR5 gene in human cells. Also, genomic DNA from reconstituted NOD-scid IL2rγnull mice spiked with the CCR5 donor DNAs did not lead to spurious amplification, showing that possible persistence of donor DNA does not lead to any PCR artifact (Figure 3b).
In the mice engrafted with human hematopoietic cells, we detected CCR5 modification in the bone marrow, spleen, thymus, small intestine, liver and lung of nanoparticle-treated mice, with only low to negligible gene modification detected when naked oligonucleotides were used (Figure 4a). These results suggest that PLGA nanoparticles become widely distributed throughout the mouse, where they are taken up in human cells, allowing for reliable gene modification, which was not achievable with equivalent dosages of naked oligonucleotide. These results are consistent with previous studies that demonstrate rapid clearance of free oligonucleotides after intravenous injection.25
To show that site-specific gene modification occurs in relevant human cell populations, CD4+ human T cells and CD34+ human HSPCs were sorted from the spleens and bone marrow, respectively, of reconstituted mice that had been treated with nanoparticles or naked oligonucleotides (Figures 4b and c). Modification was detected in sorted cells, with nanoparticle-treated mice showing significantly greater levels of gene modification than the mice injected with naked PNAs/DNAs (Figures 4d and e). Unlike what was seen in vitro, we have not seen significant differences between unmodified nanoparticles and nanoparticles surface-modified with TAT in vivo. This may be due to reduced release kinetics of TAT-modified nanoparticles as shown in Figure 1c. However, because of the robust activity of unmodified nanoparticles, we continued using the unmodified delivery system.
We used additional methods to confirm modification with the nanoparticles, and also tested for toxicity and effects on pluripotency. Mononuclear cells harvested from the bone marrow and spleens of the treated mice were able to form both myeloid and erythroid colonies with the same frequency and morphology as untreated controls (Figures 5a and b). This suggests that the nanoparticle treatment is not toxic to hematopoietic progenitors and does not affect their ability to differentiate, consistent with our previous finding that nanoparticle treatment does not affect the survival or differentiation capacity of human HSPCs in vitro.2 Individual colonies were picked for genomic DNA extraction and AS-PCR, and as each colony is theoretically derived from a single HSPC, we were able to estimate absolute modification frequencies, which were as high as 4% in the bone marrow and 19% in the spleen in this small sample set (Table 1). We confirmed the presence of the modification in one of these colonies by direct sequencing of genomic DNA (Figure 5c). Gene modification was observed in both myeloid and erythroid colonies, suggesting that gene modification using this method does not affect the differentiation capacity or survival of hematopoietic progenitors.
The treatment produced minimal off-target genotoxicity: a section of the CCR2 gene with significant homology to our target site was subjected to PCR and sequencing, and no mutations were detected in any of the 93 assayed colonies (Table 2). In addition, we performed deep sequencing to determine absolute frequencies of CCR5 gene modification and off-target CCR2 effects in cell populations within the treated mice after the in vivo nanoparticle treatments. These results are shown in Table 3. In human hematopoietic cells contained within the spleen, modification of CCR5 was 0.43%, and off-target modification of CCR2 was only 0.004%. In the bone marrow, modification of CCR5 was 0.05%, and off-target modification was more than 80 times less.
We also found that nanoparticles were capable of modifying true hematopoietic stem cells, as confirmed by serial transplant. Mice were treated as described above with PNA/DNA-containing nanoparticles by tail vein injection, or left untreated, and after 8 days (to allow for targeted modification), bone marrow was harvested from six mice (three per group) to transplant into secondary recipients (two per group) (Figure 6a). Donors had engraftment of human hematopoietic cells at high levels as determined by quantitative flow cytometry of peripheral blood (Figure 6b). The donor mice that had been treated with PNA/DNA-containing nanoparticles showed the presence of both targeted modifications in the bone marrow, consistent with results above (Figure 6c, lane 2). Of the recipient mice, one mouse receiving cells from the untreated mice and one mouse receiving cells from the nanoparticle-treated mice had engraftment of human cells as determined by the presence of the human CCR5 gene by flow cytometry (Figure 6c, lanes 4 and 5). The engrafted mouse receiving cells from the treated donor also showed the presence of the DNA donor 2-targeted modification in cells from the bone marrow, showing that this modification was present in the engrafting cells in the serial transplant, indicating persistence in the stem/progenitor cell compartment (Figure 6c, modification 2, lane 5). In addition, deep sequencing of DNA from the bone marrow obtained from this recipient mouse confirmed the presence of the CCR5 modification, with 8 out of 43 857 sequenced alleles showing the targeted change.
Next, we confirmed that nanoparticle treatment leads to CCR5 modification at the mRNA and functional levels (based on HIV-1 resistance), and does so with minimal induced inflammatory response (Figure 7). We first confirmed the expression of sequence-modified CCR5 mRNA in blood cells of treated mice by AS-reverse-transcription (RT)-PCR (Figure 7a). Next, adult NOD-scid IL2rγnull mice were engrafted with primary human peripheral blood mononuclear cells (PBMCs) heterozygous for the Δ32 mutation in the CCR5 gene. This PBMC model was used because T cells from primary human PBMCs are activated, resulting in high levels of CCR5 expression. Also, cells heterozygous with the Δ32 mutation only require one more additional CCR5 allele to be modified for total CCR5 knockout and HIV-1 resistance. After engraftment, these mice were treated with PNA/DNA-containing nanoparticles or blank nanoparticles (no oligonucleotides), and challenged with HIV-1 infection. Importantly, the mice treated with the PNA/DNA nanoparticles showed some resistance to infection, with preservation of CD4+ cell counts, consistent with resistance to HIV-1-mediated cytotoxicity of CD4+ lymphocytes (Figure 7b). As shown, mice treated with PNA/DNA nanoparticles showed preservation of CD4+ counts at levels more than twice as high as control mice that had been treated with blank nanoparticles containing no oligonucleotide therapeutic. In addition, there was no difference in the expression levels of two inflammatory cytokines after nanoparticle treatment (Figure 7c, d), suggesting relatively low inflammatory response in these mice.
To demonstrate the flexibility of our approach, we produced nanoparticles targeting a different gene, human β-globin (Figure 8). We formulated nanoparticles encapsulating PNA/DNA sequences designed to introduce a 6 bp modification at a site commonly associated with thalassemia in the human β-globin gene using previously designed donor DNA and PNA molecules (Figure 8a).13 The targeted modification was detected only by AS-PCR in mice reconstituted with human cells (Figure 8b). In addition as a control, β-globin-specific particles did not mediate site-specific modification in CCR5, or vice versa (Figure 8c). Mice that were killed both 5 and 10 days post-treatment had detectable β-globin gene modification in human blood cells in the bone marrow, spleen and lung (Figure 8d).
In addition, we synthesized nanoparticles containing PNAs and DNAs targeting another common mutation in β-thalassemia, a C to T mutation in βIVS2-654. We tested these nanoparticles in transgenic mice, enhanced green fluorescent protein (EGFP)-654,26 whose cells ubiquitously express a modified EGFP gene, which contains the aberrantly spliced intron from human β-globin, preventing EGFP expression. Correction of the IVS-654 splice-site mutation in the β-globin sequences in the fusion gene results in correct splicing and production of EGFP. After treatment with nanoparticles by tail vein injection, treated mice showed EGFP expression in cells from the bone marrow (Figure 8e), using both antisense and sense-sequence donor DNA molecules. For both antisense and sense DNA, when the nanoparticles also contained triplex-forming PNAs, there was substantially increased EGFP expression, with PNA no. 1 being more effective than PNA no. 2.
Although it is known that polymer nanoparticles similar to those used here have extensive in vivo biodistribution,27, 28 the mechanism of nucleic acid delivery via biodegradable nanoparticles is largely unknown. We have previously shown uptake of fluorescent nanoparticles into cells in the bone marrow after intravenous injection.29 Here, we again found particle uptake in the bone marrow 6 h after injection (Figure 9), which was not detectable after 24 h, suggesting clearance over this time period. As nucleic acid cargo from the PNA/DNA nanoparticles is released relatively rapidly in aqueous solution,2 we assume that intracellular nucleic acid delivery occurs within the first few hours after nanoparticle administration. This is consistent with previous biodistribution studies demonstrating that PLGA nanoparticles are rapidly cleared from the blood (half-life of seconds to hours), with longer persistence in the bone, lung, spleen and liver.30
We report here the development of a new technology for direct in vivo site-specific gene editing for the treatment of human disease, using synthetic biodegradable nanoparticles containing triplex-forming PNAs and donor DNAs. This work provides the first demonstration of direct in vivo site-specific gene editing in human cells in a chimeric mouse, and we were able to modify difficult-to-target hematopoietic progenitor cells. We have shown that intravenous injection of PLGA nanoparticles loaded with PNAs/DNAs can produce specific gene modification in the CCR5 gene in human hematopoietic cells and in clinically relevant cell types throughout a humanized mouse, including CD34+ hematopoietic progenitors, CD4+ T cells and engraftment-capable hematopoietic stem cells.
By deep sequencing, we determined the frequency of editing after direct in vivo treatment to be at least 0.05% in the bone marrow and 0.43% in the spleen, with off-target effects in the CCR2 gene 80 to 100 times less. In comparison, ex vivo treatment of human PBMCs with ZFNs led to much higher levels of modification, on the order of 35%, but the off-target mutagenesis in the CCR2 gene was on the order of 5%, only seven times less than the on-target gene disruption.31 Despite this relatively higher proportion of off-target modification, ZFNs targeting CCR5 have been approved for use in clinical trials. Hence, the much lower off-target effects of triplex-mediated gene editing should not pose a barrier to possible clinical development. While deep sequencing of the 80% homologous CCR2 gene gives an upper limit of off-target (or ‘partial-target’) gene modification, with both our technology and others, more sophisticated genome-wide screens will be necessary to determine true rates of nonspecific induction of mutations.
PCR analysis of individually picked hematopoietic colonies suggested that the targeting frequencies could be at a higher level in certain cell types as modification frequencies were higher in colony-forming cells from both the spleen and bone marrow than the frequencies determined by deep sequencing of DNA from the whole spleen and bone marrow cell populations. Several possibilities may help to explain this discrepancy. First, the smaller sample size in the colony-forming cell assay may have led to falsely inflated modification rates due to the statistical fluctuations inherent in small samples sizes. Second, it may be possible that certain cell types, such as myeloid colony-forming cells, are more susceptible to modification than other cell types. As colony-forming progenitors form a small subpopulation within the bone marrow and spleen, it is feasible that modification frequencies could be higher in these cells without significantly increasing the overall modification rate. If this is the case, the mechanism of increased modification remains to be determined, and further studies in both the chimeric and transgenic model systems may help identify other cell types that may also exhibit increased susceptibility to modification. Nonetheless, the modified progenitors were able to differentiate into various hematopoietic colony types and the injected mice showed no inflammatory response in the lung, an indication that nanoparticle treatment in vivo was relatively non-toxic.
While simple unmodified PLGA nanoparticles proved to be effective, there was no additional advantage to using cell-penetrating peptides on the surface of the particles, possibly due to slower release kinetics from these nanoparticles. Multiple methods, including direct sequencing and mRNA expression (AS-RT-PCR), were used to confirm the presence of the targeted modification using the PLGA nanoparticles.
We were also able to use this technology for site-specific editing of the β-globin gene in vivo, both in human cells and in a transgenic EGFP reporter system, demonstrating the versatility of our method. The frequency of gene editing achieved in CCR5, as determined by deep sequencing, was similar to those we achieved in the EGFP reporter, as determined by quantitative flow cytometry. In the EGFP reporter system, the activity of nanoparticles containing both donor DNAs and PNAs was higher than that of nanoparticles containing donor DNA only. The increase in gene modification with PNA addition in vivo is consistent with our previous findings in vitro with both CCR5 and β-globin gene modification. However, it is important to note that, both in vitro and in vivo, some gene modification occurs even without the addition of PNA molecules to the nanoparticles. This finding suggests that the nanoparticle system may be useful for delivery of DNA molecules alone for small fragment homologous recombination, which has been used by other groups for gene modification in several model systems including human β-globin,32 or for delivery of other nucleic acid molecules such as mRNAs or plasmids expressing ZFNs or TALENs.
In addition, preliminary studies in activated, PBMC-engrafted mice showed functional effects of CCR5 modification in terms of resistance to HIV-1 depletion of CD4+ T cells, although further experiments will be necessary to fully characterize efficacy and toxicity in this system. Because of the short-lived time span of human cell proliferation in the PBMC-engrafted mice, we were limited in the ability to perform multiple nanoparticle treatments, but our experiments here suggest that multiple treatments over a longer time span could help develop even larger populations of cells resistant to HIV-1 infection. When our biodegradable nanoparticles are used, multiple treatments are possible, and gene editing frequencies may be cumulative. Thus, although the CCR5 modification frequencies are less than those reported for ZFNs, the simplicity and gentleness of this treatment system offer the possibility for multiple treatments to achieve more significant effects. Nonetheless, we were able to observe some preservation of CD4+ T-cell levels in the nanoparticle-treated mice in the face of HIV-1 infection, so even the low frequencies of modification produced in short-term nanoparticle treatment was seen to yield measurable functional effects in vivo.
In comparison, ex vivo treatment with ZFNs was able to achieve higher levels of CCR5 disruption, with subsequent production of HIV-resistant chimeric mice after transplant of the modified human cells.3, 31 However, several advantages do exist for PNA/DNA-containing nanoparticles for gene modification, including the more favorable on-to-off target modification ratio discussed above. In addition, the nanoparticle delivery technology may be useful for diseases in which ex vivo harvest and re-transplantation of modified cells is not an option, such as in cystic fibrosis. Finally, our technology is designed for specific modification of base pairs, rather than simple gene disruption or full-gene knock-in, for treatment of diseases in which regulation of the mutant gene is important for patient survival.
Several avenues still exist for the possible improvement of this nanoparticle delivery system. Once genome modification occurs, it will persist in the cell progeny, so we do not necessarily need sustained release of our nucleic acid cargo. However, sustained release of nucleic acid cargo may allow more opportunity for genome modification as cells go through multiple rounds of cell division. The use of new polymer blends or polymers such as PLGA with poly-L-lysine,19 PBAE/PLGA blends33 or new poly-(amine-co-ester) formulations34 could help tune release kinetics of our nanoparticles. In addition, our group has developed methods for extensive surface modification, which may enhance cell-specific targeting and/or uptake of nanoparticles.20, 35
In summary, we have developed a nanoparticle-mediated approach for gene editing that is virus-free, non-toxic, has low genotoxicity, can be readily re-engineered to target different genes, targets cells in multiple organs with simple injection and mediates site-specific modification rather than gene knock-in. This type of direct in vivo gene editing technology could be used to target cells that are difficult to grow ex vivo, treat diseases that involve multiple organ systems or easily perform multiple treatments to increase overall gene modification frequency. This technology could also be expanded to deliver nucleic acid payloads such as plasmids, small interfering RNA or microRNAs to difficult-to-target human cells in vivo, providing a new methodology that could open up many new avenues of research in both the study and treatment of human disease.
All donor DNA are 5′ and 3′ end protected by three phosphorothioate internucleoside linkages. In the PNA, ‘O’ represents the 8-amino-2,6-dioxaoctanoic acid linker and ‘J’ stands for pseudoisocytosine, a replacement for cytosine that allows pH-independent triplex formation. Donor DNA was purchased from Midland Certified Reagent Company (Midland, TX, USA) and PNA was purchased from Bio-Synthesis (Lewisville, TX, USA), or Panagene (Daejeon, South Korea). CCR5- and β-globin-targeted PNA and DNA sequences are given in Figures 1 and 8. Sequences for PNA and DNA targeting the IVS2-654 site are as follows: donor DNA, 5′-IndexTermAAAGAATAACAGTGATAATTTCTGGGTTAAGGCAATAGCAATATCTCTGCATATAAATAT-3′; 654PNA1, N terminus-KKK-JTTTJTTTJTJT-OOO-TCTCTTTCTTTCAGGGCA-KKK-C terminus; and 654PNA2, N terminus-KKK-JJJTJJTTJT-OOO-TCTTCCTCCCACAGCTCC-KKK-C terminus.
PLGA nanoparticles were formulated by a double-emulsion solvent evaporation technique as described previously.2 In all, 40 nM of PNA and 40 nM of DNA in 61.6 μl dH2O were added dropwise to a polymer solution of 80 mg 50:50 ester-terminated PLGA dissolved in 800 μl dichloromethane, and then sonicated. This first emulsion was then added dropwise to 1.6 ml 5% polyvinyl alcohol, and sonicated again. The final mixture was added to 20 ml of 0.3% polyvinyl alcohol, stirred at room temperature for 3 h to evaporate the dichloromethane and then nanoparticles were collected, washed, frozen and lyophilized. Surface modifiers were added to the second emulsion at 4 nM DSPE-PEG-ligand per mg PLGA. Although equal nmoles of DNA were delivered to each treatment group, this corresponds to different milligram quantities of nanoparticles because of variability in loading. Loading of CD particles was 0.584±0.01 nM mg−1, loading of DP particles was 0.308±0.005 nM mg−1, loading of AP particles was 0.307±0.005 nM mg−1 and loading of TAT particles was 0.293±0.008 nM mg−1.
Animal use was in accordance with the guidelines of the Institutional Animal Care and Use Committee (IACUC) of the University of Massachusetts Medical School, Yale University and The Jackson Laboratories. NOD-scid IL2rγnul mice were obtained from the research colony maintained at The Jackson Laboratory. CD34-reconstituted NOD-scid IL2rγnull mice were generated by intracardiac injection of cord blood-derived human CD34+ cells into newborn mice as described previously.36 At 12 weeks post transplant, mononuclear cells from peripheral blood were harvested by eye bleeds for staining and flow cytometry analysis for the presence of human cell markers to confirm engraftment. In all, 5 mg of nanoparticles were resuspended in 200 μl phosphate-buffered saline (PBS) with brief water sonication, and injected via tail vein. Mice were killed 5 or 10 days post-treatment, and organs/cells harvested and frozen for subsequent analysis.
The 654EGFP transgenic mice were obtained from Ryszard Kole and Rudolph Juliano at the University of North Carolina, and bred and maintained at the Yale University animal facilities in the Boyer Center for Molecular Medicine according to the guidelines of the IACUC of Yale University.
The Miltenyi Beads Kit catalog no. 130-045-702 (Miltenyi Biotec, Auburn, CA, USA) was used to isolate human CD4+ cells from splenocytes from each homogenized mouse spleen as per the manufacturer’s protocol. Human CD34+ cells were isolated from mouse bone marrow using the Miltenyi Beads Kit catalog no. 130-045-702 as per the manufacturer’s protocol. For serial transplant experiments, mouse CD45+ cells were removed from the bone marrow using Miltenyi Beads Kit catalog no. 130-042-301.
Genomic DNA extraction
Genomic DNA was isolated from frozen cells or organs using a phenol–chloroform extraction method. Organs/cells were digested overnight in 10 mM Tris-HCl (pH 8), 150 mM NaCl, 20 mM ethylenediamine tetracetic acid and 1% sodium dodecyl sulfate, with proteinase K. Digests were subjected to extraction with phenol/chloroform/isoamyl alcohol followed by re-extraction with choloroform, precipitated with KoAc in EtOH, spun down and dried at room temperature and resuspended in dH2O.
Equal amounts of genomic DNA from each sample were subjected to AS-PCR, with a gene-specific reverse primer and an allele-specific forward primer in which the 3′ end corresponds to the 6 bp modified sequence; primers and reaction mixes are as described previously.813 Quantitative PCR was performed using a Stratagene Mx 3000P cycler (Agilent Technologies, Santa Clara, CA, USA); 0.2 μM donor DNA was used in spiking experiments. PCR products were separated on a 1% agarose gel and visualized using a gel imager. Primer sequences and cycler programs are available on request. Relative gene modification was calculated using the 2−ΔΔCt method, with the average of the untreated controls used as the reference groups.24
Bar-coded PCR amplicons were generated spanning a 100 bp region of the CCR5 or CCR2 gene, with the location of the targeted modification near the center of the amplicon. Samples were ligated to adapters and sequenced on an Illumina HiSeq platform (Illumina Inc., San Diego, CA, USA), with 75 base-pair paired-end reads, at the Yale West Campus Keck Sequencing Facility.
AS-RT-PCR for CCR5
RNA extraction was performed using the RNAeasy Plus Qiagen kit (Gaithersburg, MD, USA). cDNA was then made using the Superscript III First-Strand Kit (Invitrogen, Carlsbad, CA, USA). Forward primers were designed to bind in exon 2, with AS reverse primers binding in exon 3, to guarantee cDNA rather than genomic DNA amplification. PCR reactions contained cDNA, 20% betaine (Sigma, St Louis, MO, USA), 0.2 mM dNTPS (American Bioanalytical, Natick, MA, USA), advantage 2 polymerase mix (Clontech, Mountain View, CA, USA), 0.2 μM of each primer and 2% Platinum Taq (Invitrogen). Primer sequences and cycle programs are available on request.8
Colony-forming cell assay for human cells
Bone marrow or splenocytes were plated in MethoCult H4434 Classic methylcellulose medium with recombinant cytokines for human cells (Stemcell Technologies, Vancouver, BC, Canada), which is formulated to support the growth of human hematopoietic progenitor cells into erythroid, granulocyte, macrophage or mixed colonies. Colonies were counted and harvested after 1 and 2 weeks. All individual colonies were picked directly into lysis buffer for phenol–choloroform genomic DNA extraction and subsequent AS-PCR.
PBMC mouse model and HIV infection
A total of 5 × 106 Δ32 heterozygous PBMCs were injected into adult NOD-scid IL2rγnull mice by intraperitoneal injection in 400–500 μl. At 3, 5 and 7 days post-injection of PBMCs, mice were treated with 5 mg nanoparticles (in 200 μl PBS), either with (6 mice) or without (blank, 6 mice) the CCR5-modifying PNA and DNA molecules. And at 10 days post-injection of PBMCs, four mice in each treatment group were infected with 30 pore-forming unit HIV-1BaL by intraperitoneal injection in 100 μl volume. Blood was collected in heparin by retro-orbital bleeds at various time points post-injection, and mononuclear cells were stained for the analysis of CD4 expression by flow cytometry.
Measurement of production of inflammatory cytokines
Production of tumor necrosis factor-α and interleukin-6 mRNA was measured from RNA extracted from lungs using the RNAeasy Plus kit as above and cDNA was synthesized with SuperScript II First-Strand Kit (Invitrogen). Quantitative PCR was performed on cDNA with 20% betaine (Sigma), 0.2 mM dNTPS (American Bioanalytical), advantage 2 polymerase mix (Clontech), SybrGreen, ROX and 2% Platinum Taq (Invitrogen). These primers have previously been used37 and their sequences are as follows: TNF-α, 5′-IndexTermGTGGAGATCTCTTCTTGCAC-3′ and 3′-IndexTermAGTGCCCTTAACATTCTCAAG-5′; Interleukin-6, 5′-IndexTermACTCACCTCTTCAGAACGAA-3′ and 3′-IndexTermGTCTCCTCATTGAATCCAGA-5′; and glyceraldehyde 3-phosphate dehydrogenase sense, 5′-IndexTermGAAGGTGAAGGTCGGAGT-3′ and 3′-IndexTermGAAGATGGTGATGGGATTTC-5′. The cycle conditions were 94 °C 2 min, followed by 40 cycles of 94 °C 30s, 50 °C 30s and 72 °C 1 min The 2−ΔCt method was used to calculate relative mRNA expression, with glyceraldehyde 3-phosphate dehydrogenase as the reference gene.
Graphs and statistical analysis
Graphs were created using Microsoft Excel 2007. Data averaged for multiple samples is given as the mean±standard deviation.
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We thank Hanspeter Neiderstrasser and Faye Rogers for their technical assistance and helpful discussions. We also thank John Overton, Francesc Lopez and Jennifer Yamtich for assistance with deep sequencing and analysis. This work was supported by the NIGMS Medical Scientist Training Program T32GM07205 (to NAM), the NIH Genetics Training Grant T32 GM007499 (to EBS) and the National Institute of Health grants R01HL082655 (to PMG) and R01EB000487 (to WMS). This work was also supported by F30HL110372 from the National Heart, Lung and Blood institute, and the content is solely the responsibility of the authors and does not necessarily represent the official views of the NHLBI. This work was also supported by grants from National Institutes of Health Research AI46629 (DLG, LDS, MAB), AI083911 (MAB), HL077642 (LDS), CA34196 (LDS), AI073871 (DLG, LDS), DK32520 (DLG, LDS), P30 AI042845 (MAB), and grants from the Juvenile Diabetes Foundation, International (DLG, LDS, MAB) and the Helmsley Foundation (DLG, LDS, MAB). The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official views of the National Institutes of Health.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on Gene Therapy website
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McNeer, N., Schleifman, E., Cuthbert, A. et al. Systemic delivery of triplex-forming PNA and donor DNA by nanoparticles mediates site-specific genome editing of human hematopoietic cells in vivo. Gene Ther 20, 658–669 (2013). https://doi.org/10.1038/gt.2012.82
- gene modification
- peptide nucleic acid
- gene delivery
- triple-forming oligonucleotide
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