Direct Reprogramming of Human Amniotic Fluid Stem Cells by OCT4 and Application in Repairing of Cerebral Ischemia Damage.

Amniotic fluid stem cells (AFSCs) are a type of fetal stem cell whose stemness encompasses both embryonic and adult stem cells, suggesting that they may be easily and efficiently reprogrammed into induced pluripotent stem cells (iPSCs). To further simplify the reprogramming process, the creation of AFSC-derived iPSCs using a single factor is desirable. Here we report the generation of one-factor human AFSC-iPSCs (AiPSCs) from human AFSCs by ectopic expression of the transcription factor OCT4. Just like human embryonic stem cells, AiPSCs exhibited similar epigenetic status, global gene expression profiles, teratoma formation and in vitro & in vivo pluripotency. Our results indicate that the OCT4 is necessary and sufficient to directly reprogram human AFSCs into pluripotent AiPSCs. Moreover, reflecting the similar memory characteristics of AFSCs and neural stem cells, we show that AiPSC membrane-derived vesicles (MVs) repair cerebral ischemia damage. We anticipate that the successful generation of one-factor AiPSCs will facilitate the creation of patient-specific pluripotent stem cells without the need for transgenic expression of oncogenes. Moreover, MVs from tissue-specific AiPSCs have potential in tissue repair, representing a novel application of iPSCs.

Introduction

The generation of induced pluripotent stem (iPSCs) cells from mouse 1 and human 2 somatic cells by epigenetic expression of defined factors has potential application for generating patient-specific iPSCs and stem cell treatment 1-4. The molecular mechanisms underlying iPSC reprogramming remain incompletely understood due to several variables within the system, such as the number of exogenous factors required and the heterogeneity of target cells. Given that reactivation of the Myc oncogene in mice frequently causes tumours in chimeras and offspring derived from iPSCs 4, alternative approaches are required for iPSC generation that will avoid the use of oncogenes as transgenes and use the least factors. For example, one-factor iPSCs have been generated by overexpression of OCT4 only in both mouse 6 and human 7 neural stem cells (NSCs). NSC derived iPSCs generated from Human NSCs are normally isolated from fetal brain tissue however, the limited supply limits the clinical application of one-factor iPSCs derived from human NSCs.

Amniotic fluid is known to contain multiple cell types derived from the developing fetus, some of which can be reprogrammed into iPSCs. For example, IPSCs have been generated from human amniotic fluid-derived cells using four-factor 8 and two-factor (OCT4 and SOX2) 9 reprogramming systems without the use of oncogenes. A more recent report has described the isolation of a novel type of human amniotic fluid stem cells (AFSCs) 10, which represent 1% of the population of cells obtained from amniocentesis, and whose stemness encompasses both embryonic stem cells (ESCs) and adult stem cells. AFSCs are multipotent, and are characterized by expression of the receptor for stem cell factor c-Kit (CD117), in addition to OCT4, SOX2, NANOG and SSEA-4. These data led us to consider the possibility of using AFSCs to generate amniotic stem cell-derived one-factor human iPSCs, or AiPSCs.

Membrane-derived vesicles (MV)s are small vesicles released from the plasma membrane that, depending upon their cell type of origin, possess the capacity to repair local tissue damage and to modulate local tissue processes, such as angiogenesis 11-14. Embryonic stem (ES) cells are a rich source of MVs and ES-derived MVs contain a variety of stem cell-specific molecules that modulate the growth of target cells and contribute to cell-fate decision 15. Accordingly, given the similarity in memory characteristics between AFSCs and NSCs, we hypothesized that MVs isolated from AiPSCs would support both expansion of pluripotent stem cells, and mediate the repair of neuronal damage.

In this study, we describe the generation from human AFSCs of four one-factor (OCT4) human AiPSC cell lines (1F AiPSCs) and 18 two-factor (OCT4 & SOX2) human AiPSC cell lines (2F AiPSCs). We found that the majority of these cell lines maintained a normal karyotype after propagation through up to 35 passages, and expressed a complement of pluripotency markers similar to that of embryonic stem cells. Moreover, the cells were efficiently differentiated into all three germ layer cells in vitro, and were found to be capable of teratoma formation in vivo. Finally MVs isolated from AiPSCs were used to repair cerebral ischemia damage and reduce infarct area relative to control animals. Our results indicate that OCT4 is necessary and sufficient to directly induce pluripotency in AFSCs, and that MVs derived from AiPSCs have therapeutic potential in the treatment of cerebrovascular disorders.

Materials and Methods

Culture and Inactivation of mouse embryonic and human foreskin fibroblasts

Mouse embryonic fibroblasts (MEF) were isolated from BALB/c mice obtained from the Chinese Academy of Sciences, at 13 or 14 d.p.c. (day post-coitum). MEFs and human foreskin fibroblasts were grown on T-75 flask in DMEM (Gibco, Rockville, MD) containing 10% fetal bovine serum (FBS), 1% glutamine and 1% penicillin-streptomycin (Gibco), at 37 0C under a 5% CO2 atmosphere. For inactivation, MEF was incubated with 10 μg/ml of mitomycin C containing medium for 2 hour at 37 °C. Initiative MEF was plated at a density of 50,000 cells/cm2 on 6-well plate or 100mm culture dish and readied for use.

Isolation and Culture of human AFSCs and human ESC

Human AFSCs were isolated from human amniotic fluid (19-21 week gestation). Human AFSCs samples collection with written consent of subjects and the written approval from the Ethical Review Board. All experimental procedure using Human AFSCs samples in this study was reviewed and approved by the ethics committee.

Each time, 5 ml of human amniotic fluid was used for isolation of human AFSCs. After PBS washing and centrifuge, the cells were on Petri dishes in human AFSC culture medium: α-MEM medium (Gibco, Rockville, MD) containing 15% fetal bovine serum (FBS) (Gibco), 1% glutamine and 1% penicillin/streptomycin (Gibco), supplemented with 18% Chang B and 2% Chang C (Irvine Scientific Santa Ana, CA) at 37 0C under a 5% CO2 atmosphere. After initial 5-7 days, small amount of cells were attached then the attached cell expanded for 5 days ready for immunoselection by c-Kit. For immunoselection of c-Kit-positive human AFSCs, after Trysin-EDTA digestion, the cells were selected with monoclonal anti-CD117 directly conjugated to MicroBeads (Miltenyi Biotec, Auburn, CA). Human AFSCs were subcultured routinely at a dilution of 1:5 and propagated at about 70% of confluence for every 2-3 days.

The human ESC cell line ShhES2, a kind gift from Prof. Ying Jin 16 was grown on MEF (Mouse embryonic fibroblast) in human ESC culture medium comprised of Knockout-DMEM (Gibco) supplemented with 20% serum replacement (Invitrogen), 1 mM glutamine, 0.1 mM β-mercaptoethanol, 0.1 mM non-essential amino acids, 50 U/ml penicillin plus 50 μg/ml streptomycin and 4 ng/ml bFGF (Invitrogen).

Generation of 1F and 2F AiPSCs from human AFSCs

For lentivirus production, cDNAs encoding human OCT4 and SOX2 in EF1 vector containing a GFP report gene (a kind gift from Prof. Lei Xiao 17, Shanghai Institutes for Biological Sciences, SIBS) were co-transfected with packaging-defective helper plasmids into 293T cells using the LipoD293II (SignaGen, Gaithersburg, MD). Virus-containing supernatants were collected 48 h after transfection. The virus titer was adjusted to the ratio of ten virus liting a cell, which was judged by flow cytometry. For viral transduction, 2×104 human AFSCs were seeded on a 6-well plate. After the cells were evenly distributed on the culture dishes, OCT4 or OCT4 & SOX2 viruses was added into the medium with polybrene for infection overnight. 24 h later, the medium was changed with fresh AFSC culture medium and after three days the cells were subjected to a second round of infection. The infection efficiency was judged by the percentage of GFP-positive cells using flow cytometry. Using this protocol, almost 100% infection efficiency was obtained. The second-round infected human AFSCs were cultured on 60mm culture dish in AFSCs medium without mouse embryonic fibroblast (MEF) cells. After approximately 2 weeks, the cells were reduced in size, and assumed a round shape with cluster-like growth, at which point they were plated onto MEFs in a 100mm culture dish in human ESC culture medium for 2-3 weeks. Upon the appearance of large colonies with typical ESC cell morphology (a high nucleus-to-cytoplasm ratio), colonies were mechanically divided and re-plated several times on to new feeder layers.

Flow cytometry

Surface markers were stained by incubating cells with each corresponding antibody for 30 min in dark according to the product instructions. Each test included an isotype-matched negative control. Cells were then washed twice with PBS containing 1% FBS and resuspended in 0.5 ml PBS. Flow cytometry was performed on a FACScan flow cytometer (Beckman Coulter, CA). Mouse monoclonal antibodies were obtained from the sources indicated: CD73, CD29, SSEA-3, SSEA-4, Tra-1-60 and Tra-1-81 (eBioscience, San Diego, CA); CD90, CD105, CD106 and CD45 (Biolegend, San Diego, CA); CD34 (BD Pharmingen, San Diego, CA); CD133 (Miltenyi Biotech). Primary antibodies were diluted to the concentration recommended by the supplier (generally 1 μg/ml).

RT-PCR analysis

Total RNA was extracted from cells using a Mini RNeasy Kit (QIAGEN GmbH) according to the manufacturer's instructions. For reverse-transcription-polymerase chain reaction (RT-PCR), ThermoScript RT-PCR (Invitrogen) was used to synthesize cDNA from 1 μg total RNA. PCR reactions were carried out by mixing 1 μl of cDNA template, 250 nM of each primer, 200 μM dNTP mixture, and 1 U of Taq DNA polymerase in a volume of 20 μl. Samples were amplified in a thermocycler using the house keeping gene GAPDH as an internal standard. Primer information is offered (Supplementary Table S1). For expression of markers in human AFSCs, RT-PCR was performed on five human AFSC cell lines and a human ESC cell line (positive control), using primers against OCT-4, SOX2, NANOG, KLF4, C-MYC, REX1, and LIN28. For characterization of human AiPSCs cells, RT-PCR assays of AFSCs (negative control), 1F AiPSCs, 2F AiPSCs and human ESC (positive control), were performed using primers against endogenous OCT4, endogenous SOX2, NANOG, KLF4, C-MYC, REX1 and LIN28.

Immunofluorescence Staining

Cells grown in 8 well glass chamber slides (Nalgene Nunc, International) were washed twice in PBS and fixed in 4% paraformaldehyde for 30 min, followed by permeabilization with 0.1% Triton-X-100 in PBS for 5 min at room temperature (RT). Cells were blocked for 30 min in 3% BSA in PBS. All primary antibodies were diluted in the same blocking buffer and incubated with samples overnight at 4°C. Primary antibodies were obtained from the sources indicated: OCT4, SOX2 and NANOG (Santa Cruz, Santa Cruz, CA); SSEA-3, SSEA-4, Tra-1-60 and Tra-1-81 (eBioscience, San Diego, CA).Cells treated with fluorescently coupled secondary antibody (anti-rabbit Cy3, Jackson ImmunoResearch, 1/200) were incubated for 1 hour at RT. Nuclei were counterstained with 4,6-diamindino-2-phenylindole-2- (DAPI) (Sigma) for 3 min at RT. Preparations were viewed under a BX-60 epifluorescence micro-scope (Olympus, China), and images were captured with an Axiocam digital camera (Carl Zeiss, Jena, Germany, http://www.zeiss.com) and analyzed using KS-300 software (Imaging Associates, Thame, China).

Cytogenetic Analysis

A minimum of 20 metaphases were examined by the Reproductive Biology and Genetic Centre of the City Hospital of Suzhou. The karyotypes were captured and documented using Apply Imaging System for cytogenetic analysis.

Microarray and DNA methylation analysis

Affymetrix human U133 plus 2.0 array chips were used for analysis of global gene expression. For global gene expression analysis in human AFSCs (negative control), 1F human AiPSCs, 2F human AiPSCs, human ES cells (positive control), three samples for each type of cells and three technical replicates for each sample were analyzed in the microarray assay. The Sequenom EpiTYPER method was used to analyzing DNA demethylation patterns of the OCT4, SOX2 and NANOG gene promoter regions. Promoter region information is provided (Supplementary Table S2). Both experiments were performed and analyzed at the BeiJing CapitalBio Corporation. Samples of three biological repeats from human AFSCs, 1F & 2F human AiPSCs and a human ESC line (SHhES2), were collected and analyzed as described in the Affymetrix Technical and Sequenom EpiTYPER Manual.

Isolation and biological activity analysis of MVs

Culture media were collected every 48 h and centrifuged at 3,000 x g for 30 min to remove cellular debris. Supernatants were centrifuged at 100,000 x g for 2 h. Pelleted AiPSC-MVs and Fib-MVs were washed in cold PBS supplemented with 5m MHEPES and their concentration estimated by Bradford assay. To test the biological activity of the AiPSC-MVs, cells were seeded on cover slips and nuclei were stained with DAPI (Sigma) by adding dye to culture medium for 5 min. AiPSC-MVs were stained with 4x10-7M PKH26 Red Fluorescent Cell Linker Mini Kit for General Cell Membrane Labeling (Sigma) after which they were neutralized by the addition of serum, washed with PBS and added to the culture medium. Cells were incubated with PKH26 stained MVs for 5 min, 30 min, 5 h, and 10 hours or with PKH26 only. After washing with PBS the cover slips were mounted.

Teratoma formation

For teratoma induction assay, 1x106 cells from each human AiPSC cell line were harvested and mixed with matrigel and injected intramuscularly into 8 NOD-SCID mice (from the Chinese Academy of Sciences, China). For negative control experiments, matrigel containing medium was injected intramuscularly into 3 NOD-SCID mice. All mice were treated using ethyl ether for 30 seconds before injection. After 2 month, teratomas were stained with H&E (hematoxylin and eosin).

Model of Acute Ischemic Injury

For Acute Ischemic Injury model, Healthy male Wistar rats, weighing 250-300 g and aged 3-4 months ( from the Chinese Academy of Sciences, China) were subjected to transient middle cerebral artery occlusion (MCAO). For Anesthesia of rats, chloral hydrate was intraperitoneally injected with the proportion of 300mg/kg (chloral hydrate/rat weight). The middle cerebral artery was occluded using a nylon suture filament (0.24 mm) for 2 h. Reperfusion was performed by removing the suture. Out of 72 rats subjected to focal cerebral ischemia, 16 died and 12 did not exhibit paralysis of the limbs. 4 rats out of 16 died were due to over anesthesia and the other 12 rats died because of Arterial embolism operation. The remaining rats were randomly divided into three groups (n=10 per group). For MVs injection, one week after MCAO, the rats were fixed on a stereotactic apparatus and the bregma was opened by a head scalp incision. Coordinates were marked (1 mm anterior to the skull, left margin 2.5 mm; depth 4.5-5.5 mm), and a 5 μl AiPSC-MVs suspension, PBS or Fib-MVs control was then injected into the striatum using a Hamilton syringe for 10 min. 5 days after MV injection, the brains were quickly extracted. A ~2 cm ischemic area of brain tissue was excised and post-fixed in 4% paraformaldehyde. 5-μm coronal brain slices were consecutively sampled by paraffin sections. Out of 480 slices, every 20th slice was stained to find the needle position.

Neurological behavior evaluation

Neurological behavior evaluations were measured before MVs injection and 1, 2, 3 weeks after MVs injection by the neurological severity score (NSS; Supplementary Table S3), beam balance test (BBT; Supplementary Table S4) and elevated body swing test (EBST). In EBST study, observers were from the vertical axis within 30 second of the raising rats by the tail. The experiment was followed by 1 min of rest, and the test was repeated 20 times. All rats were tested three times at different time-points and the average score was tested. (iPS-MVs treatment group=5, PBS- treatment group=5, Fib-MVs treatment group=5)

Statistical analysis

Data were presented as the mean ± standard deviation. Comparisons of neurological scores were carried out by ANOVA (F test, q test), using SPSS 10.0. The paired t-test was used for the cell count. A value of P<0.05 indicated a statistically significant result.

Ethics Statement

In this study, human AFSCs samples collection with written consent of subjects and the written approval from the ethical review board of the first affiliated hospital in Soochow University and the city hospital of Suzhou. Duplicated written consent of subjects along written approval was kept in the hospital ethical review board office. All experimental procedure using human AFSCs samples in this study was reviewed and approved by the ethics committee.

Mice and rats are used in the present study; both were handled in strict accordance with good animal practice and all animal work. All experimental procedure of using mice and rats in this study was reviewed and was approved by the ethical review board of the first affiliated hospital of Soochow University.

Results

Derivation and characterization of human AFSCs

We firstly used flow cytometry to assess evaluate the expression of ESC and adult stem cell markers in human AFSCs (Fig. . All 17 human AFSCs cell lines gave similar results. AFSCs were negative for markers of the hematopoietic lineage (CD45), endothelial cells (CD106) and hematopoietic stem cells (CD34, CD133), but were positive for surface markers characteristic of mesenchymal and/or neural stem cells, including CD29 (hyaluronan receptor), CD73, CD90 and CD105 (endoglin). Human AFSCs also were positive for stage-specific embryonic antigen (SSEA)-4, a marker expressed by ESCs, but were negative for SSEA-3, Tra-1-60 and Tra-1-81. These results indicated that human AFSCs have characteristics of both ESCs and adult stem cells. To evaluate the feasibility of producing 1F and 2F AiPSCs, we next compared the expression in human AFSCs and human ESCs of several ESC marker genes used in iPSCs reprogramming (Fig. RT-PCR analysis showed that AFSCs exhibited strong expression of MYC and Rex-1, moderate expression of OCT4, NANOG, and KLF4 and sporadic expression of SOX2, but did not express LIN28. These data indicated to us that human AFSCs expressed most iPSC reprogramming factors, and suggested that they could theoretically be reprogrammed into iPSCs using a low number of such factors.

Next, human AFSCs (~20,000 cells) in AFSCs culture medium were infected with EF1 lentiviral vector containing either human OCT4 cDNA, or a 1:1 mixture of human OCT4 and SOX2 cDNAs for OCT4 and SOX2. Using this protocol, almost 100% infection efficiency was obtained. Of three SOX2 positive AFSC cell lines tested, one was a 1F AiPSC cell line and the other two were 2F AiPSC cell lines. A total of four 1F AiPSC clones out of seven human ESC-like colonies were obtained by selecting from OCT4-infected human AFSCs (reprogramming efficiency = 0.0066%) and a total of 18 2F AiPSC clones were selected from ESC-like colonies in OCT4 and SOX2-infected human AFSCs (reprogramming efficiency = 0.03%).

To determine whether prolonged culturing would induce pluripotency in human AFSCs, untransfected human AFSCs were cultured on MEFs in human ESC medium for more than six weeks. After this period, most AFSCs had differentiated into fibroblast-like cells, without any ESC-like colonies.

Characterization of human AFSCs derived-iPSCs (human AiPSCs) cells

Of the 22 human ESC-like colonies, four were expanded over 35 passages for further characterization. RT-PCR analysis (Fig. showed that relative to parental AFSCs, 1F and 2F human AiPSCs cells expressed increased levels of OCT4, SOX2, NANOG, KLF4 and LIN28, and comparable levels of MYC and REX1. Most human ESC markers expression level of 1F and 2F human AiPSCs cells were similar to them in human ESC. Immunofluorescence staining (Fig. showed that 1F AiPSCs expressed OCT4, SOX2 and NANOG transcription factors and the human ESC stage-specific surface markers SSEA3, SSEA4, TRA-1-60 and TRA-1-81. For evaluation of chromosomal abnormalities of human AiPSCs cells, cytogenetic analysis was performed using metaphase spreading. 1F and 2F human AiPSCs (AFS derived iPS) cells kept normal karyotypes during reprogramming. To exclude the possibility that iPSCs cell clones arose from human ES cell contamination, the genotypes of human AFSCs (46 XX) and AiPSCs (46 XX) and SHhES2 cells (46 XY) were confirmed, further verifying the identity of our AiPSCs cells (Fig. .

Global gene expression analysis and DNA methylation analysis in human AiPSCs

We next performed global gene expression analysis on human AFSCs, 1F and 2F human AiPSCs and human ESCs. Heat mapping (Fig. hierarchical clustering (Fig. and scatter plot analysis (Fig. indicated that the global expression profiles of 1F and 2F human AiPSCs cell were similar to those in human ESCs, but distinct from the parental AFSCs. Based upon these results, we concluded that human AFSCs were successfully reprogrammed into AiPSCs by OCT4 alone, or by OCT4 and SOX2.

We next used Sequenom EpiTYPER analysis to compare the DNA methylation patterns of the OCT4, SOX2 and NANOG promoters between the different cell lines (Fig. . We found that compared to AFCSs, 1F and 2F human AiPSCs cells and ESCs had lower levels of methylation in the promoter regions of all three genes. Unexpectedly, although SOX2 expression was weak or negative in AFCSs, we found that the extent of demethylation of the SOX2 promoter in AFSCs was higher than in human ESCs, a result we confirmed using primers to amplify other sequences in the SOX2 promoter region. It is conceivable that in these cells, although the SOX2 promoter region is transcriptionally competent, other mechanisms are acting to restrict expression of SOX2.

In vitro and in vivo pluripotency of human AiPSCs

In vitro pluripotency of 1F and 2F human AiPSCs cells was tested by embryoid body (EB) formation (Fig. . During EB period, human AiPSCs cells were easy to form globular structure with a variety of cell types. RT-PCR analysis confirmed the expression in AiSPCs of markers for endoderm (PAX6 and AFP), mesoderm (ANP and Brachyury), ectoderm (Nestin) and trophectoderm (Cdx2) (Fig. . We next evaluated the in vivo pluripotency of AiPSCs cells by subcutaneous transplantation into NOD-SCID mice. Two month after injection, all 8 NOD-SCID mice injected with 1F and 2F human AiPSCs cells grew teratomas and three negative control mice grew without teratomas. During two mouths, the mice with teratomas became thin due to tumor and the negative control mice seem normal health. All mice did not exhibit signs of pain/distress. The Size of all teratomas was around 5x8 mm. The derivatives of all three germ layers were found in the teratomas formed from 1F and 2F human AiPSCs cells, including endoderm (intestinal epithelium), mesoderm (cartilage) and ectoderm (neural epithelium, keratinized stratified squamous epithelium). (Fig.. To exclude the possibility of pluripotent cells existing in the AFSCs, a teratoma formation assay was carried out for human AFSCs and there was no evidence of teratoma in any samples after long term observation. These results indicated that like human ES cells, 1F and 2F human AiPSCs cells were pluripotent in vitro and in vivo.

AiPSC-MVs have biological activity and can enter cells

We next evaluated the biological activity of AiPSC-MVs. We observed characteristic PKH26 staining in AFSCs exposed to PKH26-labeled AiPSC-MVs (Figure , but not PKH26 alone (Figure , indicating that AiPSCs acted as 'physiological liposomes' by attaching to and fusing with target cells, and transferring their contents into the cytoplasm.

AiPSC-MVs mediate repair of acute ischemic injury

Next, we assessed the response in a rat model of brain injury after ischemia to injection of AiPSC-MVs. We found that compared with the infarct volume in PBS (30.8±3.1mm3) or Fib-MVs injected animals (27.2±1.1mm3), infarct volume in the AiPSC-MVs treated group (13.7±1.4mm3) was reduced (p<0.05; Figs. ), indicating that AiPSC-MVs mediated repair of ischemic injury.

Neurological function recovery of AiPSC-MVs treated rats

AiPSC-MVs, PBS and Fib-MVs treated rats were measured for neurological function using the NSS, BBT and EBST tests (Fig. 7A-C) after injection 0, 1, 2 and 3 weeks. In the study, the neurological deficit of AiPSC-MVs treated rats were markedly improved, indicating that AiPSC-MVs promoted neurological function recovery of Acute Ischemic Injury rats.

Figure 7

AiPS-MVs promoting neurological deficit recovery. Comparison of Score in (A) NSS, (B) BBT and (C) EBST of AiPS-MVs, PBS or Fibroblast-MV treated group. The neurological behaviors of the brain ischemic rats treated by 1F AiPS-MVs were greatly improved. NSS, neurological severity score; BBT, balance beam test; EBST, elevated body swing test.

Discussion

This study demonstrates that ectopic expression of OCT4 alone is sufficient to directly reprogram AFSCs to pluripotent 1F AiPSCs. The expression profiles of selected pluripotency markers and transcription factors in 1F AiPSCs was similar to that in ESCs, as was the extent of demethylation in the OCT4, SOX2 and NANOG promoter regions. Moreover, the majority of 1F AiPSCs cells maintained normal karyotypes, even after 35 passages, and efficiently differentiated into all three germ layer cells, as well as forming teratomas in vivo.

AFSCs express high levels of SOX2, NANOG, MYC, KLF4 and low levels of OCT4. Accordingly, expression of OCT4 in AFSCs such as NSCs (neuron stem cells) would be theoretically sufficient for successful iPSCS reprogramming. The vertebrate neural crest is a pluripotent embryonic cell population derived from the lateral ridges of the neural plate during closure of the neural tube. Neural crest cells disperse from the dorsal surface of the neural tube and migrate extensively through the embryo, giving rise to a wide variety of differentiated cell types. During this migration stage, NSCs may remain in the amniotic cavity to form a small stem cell population in amniotic fluid 18. Furthermore, amniotic fluid contains a sub-population of NESTIN positive cells (<10%), and a much smaller AF sub-population of CD117 positive cells (<1%) which express pluripotency markers. SOX2-expressing AF clones have been shown to give rise to a neuron-like phenotype in culture, expressing neuronal markers such as MAP2, NFL and NSE 19. Taken together, these data indicate that a small NSC like population (<10%) is originated from CD117 positive AFSCs derived iPS cells.

Limiting the number of factors for generating iPSCs is of great significance, both to reduce the number of oncogenes such as MYC and KLF4 3,5, which can give rise to tumors in offspring, and to minimize the probability of retroviral insertional mutagenesis. Analysis of previously reported iPSCs show up to 20 retroviral genomic integrations of external transgene 3, 20. Limiting the number of factors is also important because, due to the number of exogenous factors currently required, the molecular mechanisms for reprogramming are not completely understood. Alternative approaches to generating human iPSCs other than viral transduction of transcription factors include direct delivery of recombinant proteins 21,22 and small molecules 23. Incorporating such methodologies into our 1F AiPSCs system would offer a new approach to understanding the molecular mechanisms of iPSC reprogramming by quantitative microinjection of a single transcription factor.

Previous reports of one-factor generation of iPSCs include the use of OCT4 to reprogram NSCs of mouse 6 and human 7. Human NSCs are typically isolated from limited resource of fetal brain tissue, which limits the clinical application of one-factor iPSCs from human NSCs. In our AiPSC system, the donor AFSCs were isolated from amniotic fluid which the supply source is abandoned supply in clinic, and unencumbered by ethical issues. AFSCs were resourceful and easy to build the cell bank for storage. AFSCs therefore have great potential to generate patient-specific AiPSCs for application in autologous stem cell treatment in the later development of the baby, as well as for infants in whom a genetic disorder has been detected by amniocentesis.

We also demonstrated the potential of AiPSC-MVs in promoting neural regeneration and repairing acute ischemic injury. Since AiPSCs theoretically possess the memory characteristics of NSCs in addition to ESC character, AiPSC-MVs may therefore contain signaling molecules that mediate both nerve repair and regeneration of stem cells. Ratajczak's group had shown the role and mechanism of soluble factors and MVs derived from stem cells employed as cellular therapeutics in regenerative medicine 24. The potential mechanism by which human iPS-MV improved stroke in rats, is that iPS-MV may deliver RNA and microRNA with therapeutic effects into damaged brain. There were some species specific differences in mRNA and proteins between human and rat. However, human and rat still have the compatibility of bioactive lipids such as sphningosine-1 phosphate, ceramide-1 phosphate that are enriched in MVs between both species. Both S1P and C1P have strong proangiopoietic and antiapoptotic effects. We prove the use of MVs isolated from tissue specific iPSCs able repair tissue damage without the use of iPSCs which represent a novel approach to overcoming one of the current bottlenecks in iPSC technology.

Tables S1-S4.

Click here for additional data file.