Characterisation and hierarchy of the spermatogonial stem cell compartment in human spermatogenesis by spectral cytometry using a 16-colors panel.

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
C Lapoujade, M Blanco, M Givelet, A S Gille, I Allemand, L Lenez, N Thiounn, S Roux, J P Wolf, C Patrat, L Riou, V Barraud-Lange, P Fouchet
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引用次数: 0

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 characterised 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 β2M-CD51/61-ITGA6+SSEA4+TSPAN33+THY1+CD9medEPCAMmedCD155+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 can be delineated. This highlights the importance of a multi-parametric and spectral cytometry approach. The in-depth characterisation 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.

使用16色面板的光谱细胞术研究人类精子发生过程中精原干细胞区室的特征和层次。
大约六分之一的夫妇有生育问题,其中男性不育约占一半。精子发生起源于一小部分精原干细胞(ssc),这对治疗不孕症很有意义,但在人类中仍然缺乏特征。使用16色(16-C)细胞标记面板的多参数光谱流式细胞分析,我们确定了ssc的新标记,并为揭示和解决人类精原细胞的异质性提供了见解。这组16-C标记允许鉴定具有β2M-CD51/61-ITGA6+SSEA4+TSPAN33+THY1+CD9medEPCAMmedCD155+CD148+CD47highCD7high表型的原始ssc状态,其特征接近先前通过sc-RNAseq方法定义的最原始ssc状态0和SSC1-B。人类精子发生过程中精原干细胞和祖细胞室事件的层次结构可以被描绘出来。这突出了多参数和光谱细胞术方法的重要性。睾丸细胞的深入表征应该有助于克服干细胞知识的缺乏,这阻碍了对ssc再生潜力的理解,并且是成功开发新的基于ssc的细胞疗法的关键参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences 生物-生化与分子生物学
CiteScore
13.20
自引率
1.20%
发文量
546
审稿时长
1.0 months
期刊介绍: Journal Name: Cellular and Molecular Life Sciences (CMLS) Location: Basel, Switzerland Focus: Multidisciplinary journal Publishes research articles, reviews, multi-author reviews, and visions & reflections articles Coverage: Latest aspects of biological and biomedical research Areas include: Biochemistry and molecular biology Cell biology Molecular and cellular aspects of biomedicine Neuroscience Pharmacology Immunology Additional Features: Welcomes comments on any article published in CMLS Accepts suggestions for topics to be covered
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