BackgroundMany laboratories have described the in vitro isolation of multipotent cells with stem cell properties from the skin of various species termed skin-derived stem cells (SDSCs). However, the cellular origin of these cells and their capability to give rise, among various cell types, to male germ cells, remain largely unexplored.MethodsSDSCs were isolated from newborn mice skin, and then differentiated into primordial germ cell-like cells (PGCLCs) in vitro. Single-cell RNA sequencing (scRNA-seq) was then applied to dissect the cellular origin of SDSCs using cells isolated from newborn mouse skin and SDSC colonies. Based on an optimized culture strategy, we successfully generated spermatogonial stem cell-like cells (SSCLCs) in vitro.ResultsHere, using scRNA-seq and analyzing the profile of 7543 single-cell transcriptomes from newborn mouse skin and SDSCs, we discovered that they mainly consist of multipotent papillary dermal fibroblast progenitors (pDFPs) residing in the dermal layer. Moreover, we found that epidermal growth factor (EGF) signaling is pivotal for the capability of these progenitors to proliferate and form large colonies in vitro. Finally, we optimized the protocol to efficiently generate PGCLCs from SDSCs. Furthermore, PGCLCs were induced into SSCLCs and these SSCLCs showed meiotic potential when cultured with testicular organoids.ConclusionsOur findings here identify pDFPs as SDSCs derived from newborn skin and show for the first time that such precursors can be induced to generate cells of the male germline.

Ge, W., Sun, Y., Qiao, T., Liu, H., He, T., Wang, J., et al. (2023). Murine skin-derived multipotent papillary dermal fibroblast progenitors show germline potential in vitro. STEM CELL RESEARCH & THERAPY, 14(1), 17 [10.1186/s13287-023-03243-5].

Murine skin-derived multipotent papillary dermal fibroblast progenitors show germline potential in vitro

De Felici, Massimo;
2023-02-03

Abstract

BackgroundMany laboratories have described the in vitro isolation of multipotent cells with stem cell properties from the skin of various species termed skin-derived stem cells (SDSCs). However, the cellular origin of these cells and their capability to give rise, among various cell types, to male germ cells, remain largely unexplored.MethodsSDSCs were isolated from newborn mice skin, and then differentiated into primordial germ cell-like cells (PGCLCs) in vitro. Single-cell RNA sequencing (scRNA-seq) was then applied to dissect the cellular origin of SDSCs using cells isolated from newborn mouse skin and SDSC colonies. Based on an optimized culture strategy, we successfully generated spermatogonial stem cell-like cells (SSCLCs) in vitro.ResultsHere, using scRNA-seq and analyzing the profile of 7543 single-cell transcriptomes from newborn mouse skin and SDSCs, we discovered that they mainly consist of multipotent papillary dermal fibroblast progenitors (pDFPs) residing in the dermal layer. Moreover, we found that epidermal growth factor (EGF) signaling is pivotal for the capability of these progenitors to proliferate and form large colonies in vitro. Finally, we optimized the protocol to efficiently generate PGCLCs from SDSCs. Furthermore, PGCLCs were induced into SSCLCs and these SSCLCs showed meiotic potential when cultured with testicular organoids.ConclusionsOur findings here identify pDFPs as SDSCs derived from newborn skin and show for the first time that such precursors can be induced to generate cells of the male germline.
3-feb-2023
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/17 - ISTOLOGIA
English
Papillary dermal fibroblast progenitors
Single-cell transcriptomes
Skin-derived stem cells
Spermatogonial stem cells like cells
Ge, W., Sun, Y., Qiao, T., Liu, H., He, T., Wang, J., et al. (2023). Murine skin-derived multipotent papillary dermal fibroblast progenitors show germline potential in vitro. STEM CELL RESEARCH & THERAPY, 14(1), 17 [10.1186/s13287-023-03243-5].
Ge, W; Sun, Y; Qiao, T; Liu, H; He, T; Wang, J; Chen, C; Cheng, S; Dyce, Pw; De Felici, M; Shen, W
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/330563
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