Genetic reporter analysis reveals an expandable reservoir of OCT4+ cells in adult skin
- Anne Limbourg†1, 2, 3, 4,
- Sabine Schnabel†1, 2,
- Vladimir J Lozanovski1, 2, 10,
- L Christian Napp1, 5,
- Teng-Cheong Ha2, 6,
- Tobias Maetzig2, 6,
- Johann Bauersachs2, 5,
- Hassan Y Naim7,
- Axel Schambach†2, 3, 6, 8Email author and
- Florian P Limbourg†1, 2, 9, 11Email author
© Limbourg et al.; licensee BioMed Central Ltd. 2014
Received: 4 December 2013
Accepted: 3 June 2014
Published: 14 June 2014
The transcription factor Oct4 (Pou5f1) is a critical regulator of pluripotency in embryonic and induced pluripotent stem cells. Therefore, Oct4 expression might identify somatic stem cell populations with inherent multipotent potential or a propensity for facilitated reprogramming. However, analysis of Oct4 expression is confounded by Oct4 pseudogenes or non-pluripotency-related isoforms. Systematic analysis of a transgenic Oct4-EGFP reporter mouse identified testis and skin as two principle sources of Oct4+ cells in postnatal mice. While the prevalence of GFP+ cells in testis rapidly declined with age, the skin-resident GFP+ population expanded in a cyclical fashion. These cells were identified as epidermal stem cells dwelling in the stem cell niche of the hair follicle, which endogenously expressed all principle reprogramming factors at low levels. Interestingly, skin wounding or non-traumatic hair removal robustly expanded the GFP+ epidermal cell pool not only locally, but also in uninjured skin areas, demonstrating the existence of a systemic response. Thus, the epithelial stem cell niche of the hair follicle harbors an expandable pool of Oct4+ stem cells, which might be useful for therapeutic cell transfer or facilitated reprogramming.
KeywordsOct4 Epidermal stem cells Skin Transgenic reporter mice
Regenerative cell therapy for terminally differentiated organs damaged by disease requires multipotent stem cell reservoirs, preferably from autologous sources. The POU-domain transcription factor Oct4 (Pou5f1) is an important regulator of pluripotency in embryonic stem (ES) and induced pluripotent stem (iPS) cells . The latter arise during re-programming from clones re-expressing endogenous Oct4 , while under specific culture conditions ectopic expression of Oct4 alone in primary somatic cells is sufficient for reprogramming into iPS or multilineage progenitors [3, 4]. Therefore, endogenous Oct4+ stem cells might either display inherent multipotent differentiation potential or serve as a source for minimal modification approaches to generate iPS with high efficiency. However, analysis of Oct4 expression is confounded by false-positive results due to Oct4 pseudogenes or non-pluripotency-related, non-nuclear OCT4B isoforms, explaining contradictory reports on Oct4 expression in several somatic stem cell populations .
The hair follicle, as part of the protective and self-renewing mammalian epidermis, is one of the few organs that undergoes constant cycles of degeneration and regeneration throughout life. It contains an epidermal stem cell niche harboring multipotent epidermal stem cells, which can be mobilized to regenerate the new follicle with each hair cycle or in damaged skin during wound repair . Multipotent epidermal stem cells not only give rise to new epidermis and hair when grafted but are able to correct inherited skin disease in humans and differentiate into all principle tissue lineages in culture [6–9], while a population of skin stem cells can contribute to skeletal muscle fiber regeneration in muscle dystrophy after cell transplantation . Furthermore, a poorly characterized subset of cells isolated from human hair follicles has been shown to express Oct4 and to display multipotent behavior in vitro . Our objective was to identify adult somatic stem cells expressing Oct4 using a well characterized Oct4-GFP genetic reporter mouse model as a potential reservoir for regenerative cell therapy.
To identify in a genetic screening approach OCT4+ stem cells during postnatal life, we analyzed different tissues of Pou5f1-EGFP transgenic reporter mice (called OG2) for GFP expression by flow cytometry. These mice express enhanced GFP under the control of the Oct4 promoter including the distal enhancer, and expression of GFP has been shown to serve as well described reporter for endogenous, pluripotency-related OCT4 expression in induced pluripotent stem cells as well as during development and more interestingly postnatal life [12–15].
Frequency of GFP + cells in different mouse tissues and age groups
3.58E + 06
2.83E + 07
2.46E + 07
Heart p MI
2.67E + 07
2.49E + 07
4.22E + 07
5.87E + 07
2.83E + 07
8.97E + 07
7.03E + 07
1.22E + 06
3.00E + 07
1.52E + 07
8.30E + 06
6.35E + 06
7.57E + 06
Screening of various tissues reported to harbor Oct4 expressing stem cells, such as heart and bone marrow, did not detect GFP+ cells in these tissues, although large cell numbers from each organ were analyzed (Table 1). As Oct4 expression was also found in human adipose tissue derived stem cells , we also analyzed GFP expression in the inguinal adipose tissue, but could not detect GFP+ cells in 4 analyzed animals (data not shown). However, GFP+ cells were discovered in the skin (Table 1, Figure 1C), which express the nuclear, pluripotency-related OCT4 isoform (Figure 1D). This cell population expanded transiently and in a biphasic fashion during postnatal life, peaking at puberty and early adulthood, which was reminiscent of the synchronized and cyclic activity of the hair follicle during the first hair cycles (Figure 1E). In situ, GFP+ cells localized to the bulge region of the hair follicle, which is a niche for multipotent epithelial stem cells and marked by the insertion of smooth muscle cells (Figure 1F) . These multipotent stem cells consist of a basal and suprabasal population, which behave analogously with respect to self-renewal and differentiation potential, and which are defined by expression of CD34 and high or low expression of integrin (ITG) α6, respectively . Flow cytometry of GFP+ and GFP- skin cells revealed that GFP+ cells were found in both stem cell subsets, but not in the non-stem cell compartment (Figure 1G). These data suggest that GFP expression identifies an Oct4 + population of multipotent epidermal stem cells residing in the stem cell niche of the hair follicle. Further characterization of the surface marker profile of GFP+ stem cells revealed a phenotype of Sca-1+, CD117lo, CXCR4lo and ITG β1- (Figure 1H). In contrast to GFP- cells, GFP + cells also showed evidence for Oct4 mRNA expression, as demonstrated by primers specific for exon 1, but expression levels were considerably lower than in ES or iPS controls. Interestingly, GFP+ cells also expressed low amounts of other key iPS reprogramming factors, Klf4, Sox2 and c-Myc, however, these were also present in GFP- cells (Figure 1I).
Using an Oct4-GFP transgenic reporter, we identify skin as a novel principle source of postnatal Oct4+ cells. We also confirm previous reports on the existence of OCT4+ cells in neonatal testis [12, 16–18]. However, numbers of GFP+ cells in testis decline rapidly and permanently before puberty. In contrast, the skin-resident cell pool expands postnatally in a cyclic fashion strikingly matching the time-course of the cyclic hair follicle activity during the first postnatal hair cycles, which in the mouse occurs in a synchronized fashion . In situ, GFP + cells localize into the bulge region of the hair follicle, which constitutes a niche for two populations of multipotent epidermal stem cells. Surface marker analysis demonstrates that GPF + cells are present in both stem cell subsets. Furthermore, the adult GFP + stem cell pool expands in the entire skin in response to injury or non-traumatic depilation, suggesting so far unknown systemic signals controlling stem cell expansion. This also establishes a simple but defined setting for cell expansion for therapeutic cell harvest, i.e. depilation. The here characterized Oct4 + epidermal stem cells not only express the nuclear OCT4 isoform but – albeit at very low levels – other factors of the reprogramming cocktail. Notably, epidermal stem cell populations with similar characteristics also exist in humans [11, 21]. Thus, skin might serve as a reservoir for an expandable stem cell population, which could be useful for therapeutic cell transfer or facilitated reprogramming to generate iPS ex vivo.
The functional relevance of Oct4 expression, and the biological potential of the identified cell population, requires further studies. Mice with conditional-inducible deletion of Oct4 in skin cells using the keratin K15 promoter showed normal hair follicle architecture and skin wound healing response in short-term experiments . However, the long-term consequences of Oct4 deletion were not studied. Furthermore, multipotent epidermal stem cells in the hair follicle bulge have been identified and characterized based on K14 expression , leaving open the possibility of an escape from Oct4 inactivation in this study.
Of note, Dyce and colleagues have differentiated skin-derived stem cells into oocyte-like cells, i.e. Oct4high germ cells . In light of our findings and recent reports that culture conditions strongly influence cell fate control, e.g. as for gPS, one could envision that Oct4+ skin cells have been reprogrammed under appropriate culture conditions into Oct4high germ cells, e.g. oocyte-like cells.
Importantly, just recently human multipotent dermal stem cells have been isolated based on neural crest stem cell marker nestin . Importantly, these cells were also positive for Oct4, suggesting that Oct4 positivity of dermal stem cells might be conserved across species.
Our findings of an expandable Oct4+ stem cell pool in the skin may have implications for facilitated reprogramming or for the development of new skin stem cell-based therapeutic models. In addition, if it is possible to culture Oct4+ epithelial stem cells in vitro, this will also ease genetic modification of skin stem cells to repair genetic defects, e.g. for gene therapy of epidermolysis bullosa.
Rabbit anti-Oct4 sc-9081 (Santa Cruz), mouse anti-SMA-Cy3 C6198 (Sigma), rabbit anti-GFP SP3005P (Acris), rat anti-c-kit/CD117 clone 3C1 (Miltenyi Biotec), rat anti-Cxcr4 FAB21651A (R&D Systems), rat anti-sca-1 clone D7 (Miltenyi Biotec), rat anti-α6-Integrin clone GH3 (R&D Systems), rat anti-CD34, clone MEC14.7 (Biolegend).
RT-PCR: Oct4, fwd: gcgttctctttggaaaggt, rev: agcctcatactcttctcgttgg. Rex-1, fwd: caccatccgggatgaaagtgagat, rev: accagaaaatgtcgctttagtttc. GAPDH: fwd: accacagtccatgccatcac, rev: tccaccaccctgttgctgta. Real-time PCR: Oct4, fwd: gttggagaaggtggaaccaa, rev: ctccttctgcagggctttc. Myc, fwd: cgcctagaattggcagaaat, rev: aactgagaagaatcctattcagcac. Klf4, fwd: cgggaagggagaagacact, rev: gagttcctcacgccaacg. Sox2, fwd: tgctgcctctttaagactaggg, rev: tcgggctccaaacttctct. Quantitative real-time PCR was carried out on the LightCycler 480 System (Roche).
The study was conducted with permission of the State of Niedersachsen, conforming to the German Law for the Protection of Animals and the NIH Guide for the Care and Use of Laboratory Animals. Pou5f1-egfp reporter mice (B6; CBA-Tg (Pou5f1-EGFP) 2Mnn), have been described before and were housed at SPF conditions .
Cell isolation and FACS analysis
Tissues were dispersed mechanically or digested with Collagenase I (0.25% w/v) and DNAse I (360 U/ml) for 45 min at 37 C. For isolation of skin-resident cells, mice were shaved thoroughly and abdominal, dorsal and flank skin carefully excised. Whole skin was spanned with the epidermis facing down and dermal fat mechanically removed using curved tweezers. Skin was washed in PBS, finely homogenized using surgical scalpels and digested. The released cells where recovered by centrifugation, washed several times with PBS with 2% FCS, stained with propium iodide solution and analyzed on a FACSCalibur (BD Bioscience). Specific GFP-fluorescence was discriminated from autofluorescence and dead cells by plotting FL-1 vs FL-2 with uncompensated settings.
Data are given as mean and SEM, unless stated otherwise. Comparisons were performed by Student’s t-test or ANOVA with Bonferroni’s or Dunnett’s post-test.
Embryonic stem cell
Induced pluripotent stem cells
Fluorescent activated cell sorter
Specific pathogen free
Green fluorescent protein
Fetal calf serum
Germline-derived pluripotent stem cells.
We thank T. Cantz and H. R. Schöler (Hannover/Muenster, Germany) for providing OG2 mice and ES cell cultures and valuable advice. This work is supported by funding from the Deutsche Forschungsgemeinschaft (REBIRTH EXC 62/1, SFB738), the BMBF (IFB-Tx 01EO0802), DEBRA, E-RARE and the DAAD (scholarship and German-Chinese research group).
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