Characterization and hierarchy of the spermatogonial stem cell compartment in human spermatogenesis by spectral cytometry using a 16-colors panel
Lapoujade, C.; Blanco, M.; Givelet, M.; Gille, A. S.; Allemand, I.; Lenez, L.; Thiounn, N.; Roux, S.; Wolf, J. P.; Patrat, C.; Riou, L.; Barraud-Lange, V.; Fouchet, P.
Show abstract
About one in six couples experience fertility problems, and male infertility accounts for about half of these cases. Spermatogenesis originates from a small pool of spermatogonial stem cells (SSCs), which are of interest for the treatment of infertility but remain poorly characterized in humans. Using multiparametric spectral flow cytometric analysis with a 16-colours (16-C) panel of cell markers, we identify novel markers of SSCs and provide insights into unravelling and resolving the heterogeneity of the human spermatogonial cells. This 16-C panel of markers allowed the identification of a primitive SSCs state with the {beta}-2M-CD51/61- ITGA6+SSEA4+TSPAN33+THY1+CD9+EPCAMmedCD155+CD148+CD47highCD7high phenotype, with a profile close to the most primitive SSCs states 0 and SSC1-B previously defined by sc-RNAseq approach. The hierarchy of events in the spermatogonial stem cell and progenitor compartment of human spermatogenesis has been delineated. This highlights the importance of a multi-parametric and spectral cytometry approach. The in-depth characterization of testicular cells should help to overcome the lack of stem cell knowledge, that hinders the understanding of the regenerative potential of SSCs, and is a critical parameter for the successful development of new SSCs-based cell therapies.
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