Virus free induction of pluripotency and subsequent excision of reprogramming factors
Reprogramming of somatic cells to pluripotency, thereby creating induced pluripotent stem (iPS) cells, promises to transform regenerative medicine. Most instances of direct reprogramming have been achieved by forced expression of defined factors using multiple viral vectors1-7. However, such iPS cells contain a large number of viral vector integrations1,8, any one of which could cause unpredictable genetic dysfunction. While c-Myc is dispensable for reprogramming9,10, complete elimination of the other exogenous factors is also desired since ectopic expression of either Oct4 or Klf4 can induce dysplasia11,12. Two transient transfection reprogramming methods have been published to address this issue13,14. However, the efficiency of either approach is extremely low, and neither has thus far been applied successfully to human cells. Here we show that non-viral transfection of a single multiprotein expression vector, which comprises the coding sequences of c-Myc, Klf4, Oct4 and Sox2 linked with 2A peptides, can reprogram both mouse and human fibroblasts. Moreover, the transgene can be removed once reprogramming has been achieved. iPS cells produced with this non-viral vector show robust expression of pluripotency markers, indicating a reprogrammed state confirmed functionally by in vitro differentiation assays and formation of adult chimeric mice. When the single vector reprogramming system was combined with a piggyBac transposon15,16 we succeeded in establishing reprogrammed human cell lines from embryonic fibroblasts with robust expression of pluripotency markers. This system minimizes genome modification in iPS cells and enables complete elimination of exogenous reprogramming factors, efficiently providing iPS cells that are applicable to regenerative medicine, drug screening and the establishment of disease models.
Efficient multiprotein expression has been reported in a variety of cell types, including human ES cells, using the 2A peptide sequence of foot-and-mouth disease virus (F2A), or 2A-like sequence from other viruses17,18. Recently, this multiprotein expression strategy has also been applied for reprogramming with transient transfection14 and doxycycline (dox)-inducible lentiviral vector19,20. Here we have taken advantage of the strategy to generate virus-free factor-removable iPS cells flanking a 2A-peptide-linked reprogramming cassette, c-Myc-Klf4-Oct4-Sox2 (MKOS)-ires-mOrange, by loxP sites (Supplementary Figure 1). Initially we investigated whether the 2A peptide-mediated multiprotein expression could achieve robust expression of c-Myc, Klf4, Oct4 and Sox2, when transcribed from the ubiquitously expressed synthetic CAG enhancer/promoter21. When the vector was transfected into HEK293 cells, expression of Klf4, Oct4 and Sox2 could be detected by immunoblotting (Supplementary Figure 2a). While high expression of endogenous c-Myc in HEK293 cells precluded clear identification of exogenous c-Myc, a phosphorylated form at Thr 58 that was subjected to subsequent ubiquitination22 was enriched in the transfectants, suggesting excess c-Myc was degraded (Supplementary Figure 2a, b). Appropriate nuclear localization of exogenous Oct4 and Sox2 was also observed in the transfected HEK 293 cells (Supplementary Figure 2c).
When the vector, pCAG2LMKOSimO, was introduced into MEFs, some mOrange positive cells converted to an ES cell-like morphology at day 5-6, and by day 9 colonies containing alkaline phosphatase positive cells appeared (data not shown). Moreover morphologically ES cell-like colonies picked between days 20-30 succeeded to grow maintaining an ES cell-like morphology on gelatin (Supplementary Figure 3a). We then went on to estimate the reprogramming efficiency using Nanog reactivation as a marker of reprogramming3,4. MEFs from TNG mice, which have a GFP reporter inserted at the Nanog start codon23, and MEFs from wild-type 129 mice were transfected with the pCAG2LMKOSimO plasmid and cultured on either γMEFs or gelatin. The number of transiently transfected mOrange positive cells was measured by flow cytometry at day 2. The number of reprogrammed colonies judged by GFP positivity (TNG MEFs) or anti-Nanog immunofluorescence (129 MEFs) (Supplementary Figure 3b) was scored at day 28 (Table 1). By comparing stable transfection efficiency with Nucleofection (3.6 % of transiently transfected cells, see Supplementary Figure 3c for details) and the number of reprogrammed colonies, we calculate overall reprogramming effiiency as average 2.5% (Supplementary Table 1). While the estimation method is different from that used in viral reprogramming systems (efficiency; ∼0.1% 2,3,7), this relatively high efficiency may depend on several factors in this non-viral method, including expression of the four reprogramming factors from a single transcript and use of the CAG enhancer/promoter, which may be less prone to silencing.
Stable cell lines were established by picking colonies derived from transfection of 129 MEFs (8/12 morphologically ES cell-like colonies picked) and TNG MEFs (5/9 GFP positive colonies picked) with pCAG2LMKOS
The number of vector integration sites was analyzed by Southern blotting in cell lines imO1-imO8, as well as 5 TNG iPS cell lines, TNGimO1-imO5 (strategy shown in Figure 2a). Of the 13 cell lines, imO7 and TNGimO5 were found to have a single vector integration in one site, indicating that a stable single-copy insertion of the non-viral expression vector can achieve direct reprogramming, effectively minimizing genome modification in iPS cells (Figure 2b). We did not find reprogrammed cell lines without vector integration. The integration sites of imO1, imO3 and imO7, as well as the tandem repeats in imO1 and imO3, were identified by inverse PCR and confirmed by genomic PCR (Supplementary Figure S5 and Figure 2c). All integration sites of the individual cell lines are different, supporting the notion that reprogramming does not depend upon vector integration at specific loci8. Expression of the genes at the integration sites was detectable in MEFs, ES cells, and all examined iPS cell lines, without significant influence imposed by vector integration (Supplementary Figure 5d). Adult cells (footpad fibroblasts) were also succesfully reprogrammed via definite single-copy vector integration (Supplementary Figure 6).
To remove the exogenous reprogramming factors, we performed transient Cre transfection and tracked the loss of fluorescent reporter expression. Surprisingly, many of the mOrange negative colonies started to differentiate after Cre transfection (Supplementary Figure 7a). This excision-mediated differentiation was prevented by culturing the cells in the presence of the Fgf receptor inhibitor, PD173074, which inhibits mouse ES cell differentiation25 (Figure 3a). The percentage of differentiated colonies after Cre-mediated excision differed among clones, possibly reflecting variable stability of the reprogrammed state (Figure 3b). All tested reprogramming cassette-excised clones, which were generated from imO2, imO3, imO7 and TNGimO5 and expanded in the presence of PD173074, could subsequently maintain an undifferentiated morphology for at least 5 passages after removal of PD173074 (data not shown). The presence of PD173074 may allow cells to adapt upon rapid loss of exogenous reprogramming factors in single cells at colony density. Whereas Cre-excised cell lines from imO7 and TNGimO5 could be maintained over 20 passages while maintaining an undifferentiated morphology, cell lines derived from imO2 and imO3 were prone to generate more differentiated cells at later passages in the absence of PD173074, suggesting a different reprogramming level for each clone (data not shown). The endogenous gene expression of c-Myc, Klf4, Sox2, and Oct4 was maintained in the
We next examined the differentiation ability of the cell lines before and after reprogramming cassette excision. Cre-excised cell lines imO3c8 and imO7c8 downregulated the pluripotency markers Oct4, Nanog and Rex1, and up-regulated markers of all three germ layers in embryoid bodies, thus behaving in the same way as ES cells26 (Supplementary Figure 9a). Furthermore, β-tubulin positive neurons were generated efficiently in a monolayer neural differentiation protocol27 (Supplementary Figure 9b). Differentiation of the factor-retained parental cell lines imO3 and imO7 was less efficient (Supplementary Figure 9a, b). Both imO7 and imO7c8 produced teratocarcinomas when transplanted to the kidney capsule, although imO7 tumours contained more undifferentiated cells than those from imO7c8 tumours (Figure 3c). Finally we injected the reprogramming vector-free iPS cells into C57BL/6 blastocysts (results summarized in Supplementary Table 2). To identify chimeric embryos two cell lines with constitutive
To address the reprogramming ability of the non-viral single-vector system in human cells, we enhanced stable transfection efficiencies using a piggyBac (PB) transposon gene delivery system15. Co-transfection of two PB transposons carrying a doxycycline (dox) inducible MKOS-ires-geo cassette and a constitutively active CAG-rtTA transactivator construct16 was applied to human embryonic fibroblasts (Supplementary Figure 10a). In this design, upon genomic integration, the two transposons allow dox-inducible activation of MKOS expression in wild-type cells. We observed iPS-like colony formation 14 days post transfection (dpt) when the cells were maintained in hES cell culture conditions supplemented with dox. In total, fifteen colonies were picked from 14-25dpt from four wells of 6-well plates, initially containing either 3.2×104 or 6.4×104 fibroblasts/well. When dox was withdrawn on 32dpt, three clones successfully propagated as stable cell lines, while the exogenous factor expression was uninduced as indicated by negative staining for lacZ activity (Supplementary Figure 10b). All clonal lines displayed human ES cell morphology (Supplementary Figure 10b) and were positive for alkaline phosphatase (not shown). Robust expression of endogenous pluripotency markers, SSEA4, NANOG, TRA-160 and TRA-181 was confirmed in all the three cell lines (Supplementary Figure 10c). These results demonstrate that the non-viral single-vector system can reprogram human fibroblasts and strongly suggests that it can also be applied to the production of exogenous factor-free, non-viral human iPS cells.
We demonstrate that single non-viral vector with 2A peptide-linked reprogramming factors can achieve reprogramming efficiently and the exogenous reprogramming factors can be completely removable from the iPS cells using subsequent Cre-transfection. Absolute avoidance of unpredictable exogenous reprogramming factor reactivation is important not only for clinical applications but also for drug screening, since some small molecules affect epigenetic genome modification28 which could cause unexpected reactivation and unreliable screening results. Cre recombinase boasts the most efficient in vivo and in vitro recombination system currently known, and a part of the vector backbone remained in the integration site following Cre-mediated factor deletion would be a tolerable remnant for in vitro iPS applications. We also demonstrated the single-vector reprogramming system combined with PB transposon delivery system for human cell reprogramming. PB transposons are completely removable from their integration site without any residual change in the original DNA sequence15,16. This PB-based single-vector reprogramming system will enable the generation of non-genetically modified human iPS cells as shown in the mouse16, which is ideal for regenerative medicine.
A vector, pCAG2LMKOSimO, which have c-Myc, Klf4, Oct4 and Sox2 coding regions linked with 2A peptide sequences driven by CAG enhancer/promoter18,21, were constructed as described in the Methods. The vectors were introduced into MEFs using Nucleofector II (Amaxa) and cells were cultured in ES cell culture condition for up to 4 weeks. Colonies showing ES cell-like morphology were picked and cultured either on irradiated MEFs (γMEFs) or gelatin after trypsinization. Gene expression, integration number/sites of the vector in the established cell lines were analyzed by quantitative PCR, immunoblotting, Southern blotting and inverse PCR, respectively. The reprogramming cassette was excised by Cre transient transfection in the presence or absence of an Fgf receptor inhibitor PD173074 (100 ng/ml), and pluripotency of the cell lines were examined in vitro (embryoid body formation, neural differentiation) and in vivo (teratoma formation, blastocyst injection).
Full Methods accompany this paper.
|Nucleofection condition1||2 days after nucleofection2||No. of Nanog/Nanog-GFP +ve|
colonies at day 283
|+ve cell No|
|on γMEFs||on gelatin|
12×106 MEFs from TNG or 129 mice (passage number is shown) were transfected using indicated amount of linearised DNA in each experiment.
2mOrange positive (+ve) cell number at day 2 was estimated from harvested cell number from one well and percentage of mOrange +ve cells.
3Number of Nanog-GFP colonies from TNG MEFs or Nanog positive colonies (by immunofluorescence) from 129 MEFs at day 28 on irradiated MEFs (γMEFs) or on gelatin is shown. -; no data. *; average of two wells. **; average of three wells.
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We thank A. Tsakiridis for advice on using 2A peptide sequence and A. Nagy for providing data from his laboratory on generating human reprogrammed cell lines by combining the PB transposon system and the 2A sequences joined reprogramming factors and his comments on the manuscript. We also thank I. Chambers for providing TNG MEFs, discussion and comments on the manuscript, V. Wilson for advice on teratoma analysis, T. Kunath, S. Lowell, C. Blackburn and K. Vintersten for discussions and comments on the manuscript, B. Hendrich for permission for starting preliminary experiments of this work in his laboratory. We also thank J. Ure, L. Robertson, R. McLay, and R. Wilkie for technical assistance, Biomed unit staff for mouse husbandry. K.K. is the recipient of MRC career development fellowship in stem cell research. A.P. is the recipient of a BBSRC CASE PhD studentship. M.M., P.M. and K.W. were supported by grants from the Canadian Stem Cell Network and JDRF.
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