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原索动物中的生殖系干细胞分离、谱系追踪与衰老

Germline stem cell isolation, lineage tracing, and aging in a protochordate.

作者信息

Levy Tom, Anselmi Chiara, Ishizuka Katherine J, Gordon Tal, Voskoboynik Yotam, McGeever Erin, Detweiler Angela M, Levin Liron, Palmeri Karla J, Liu Daniel Dan, Sinha Rahul, Ohene-Gambill Benjamin F, Raveh Tal, Morri Maurizio, Vanni Virginia, Manni Lucia, Sahoo Debashis, Neff Norma F, Rosental Benyamin, Weissman Irving L, Voskoboynik Ayelet

机构信息

Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA.

Department of Biology, Hopkins Marine Station, Stanford University, Pacific Grove, CA, USA.

出版信息

bioRxiv. 2025 Sep 4:2025.08.31.673173. doi: 10.1101/2025.08.31.673173.

Abstract

Germline stem cells (GSCs), the source of gametes, are the only stem cells capable of passing genes to future generations and are therefore considered units of natural selection. Yet, the factors that influence GSC fitness, and thus govern GSC competition, which exist in both protochordates and mammals, remain poorly understood. We studied how aging affects GSC fitness in the protochordate , an evolutionary crosspoint between invertebrates and vertebrates. GSCs were isolated and distinguished from developing and mature gametes using flow cytometry and scRNA-Seq, facilitated by a new PacBio genome assembly. Moreover, their function was validated through a novel lineage tracing approach that combines membrane-labeled GSC transplantation with scRNA-Seq. Leveraging our method to isolate them, single-cell transcriptomics showed significant age-related changes between young and old GSCs. Spermatids and sperm, however, showed minimal changes, suggesting that reproductive aging is governed by GSCs rather than by gametes. Reduced expressions of markers like DDX4 and PIWIL1 in aged GSCs mirrored trends in mammalian datasets, pointing to a conserved GSC-driven aging mechanism across chordate evolution. This study provides new techniques that lay the foundation to investigate further drivers of GSC fitness and highlights fertility-related genes as promising targets for therapies to preserve reproductive health.

摘要

生殖系干细胞(GSCs)是配子的来源,是唯一能够将基因传递给后代的干细胞,因此被视为自然选择的单位。然而,影响GSC适应性并因此支配GSC竞争的因素,在原索动物和哺乳动物中都存在,目前仍知之甚少。我们研究了衰老如何影响原索动物中的GSC适应性,原索动物是无脊椎动物和脊椎动物之间的一个进化交叉点。利用新的PacBio基因组组装技术,通过流式细胞术和单细胞RNA测序(scRNA-Seq)将GSCs分离出来,并与发育中的和成熟的配子区分开来。此外,通过一种将膜标记的GSC移植与scRNA-Seq相结合的新型谱系追踪方法,验证了它们的功能。利用我们分离它们的方法,单细胞转录组学显示年轻和年老的GSCs之间存在与年龄相关的显著变化。然而,精子细胞和精子的变化最小,这表明生殖衰老由GSCs而非配子控制。老年GSCs中DDX4和PIWIL1等标志物的表达降低反映了哺乳动物数据集中的趋势,表明在整个脊索动物进化过程中存在一种保守的由GSCs驱动的衰老机制。这项研究提供了新的技术,为进一步研究GSC适应性的驱动因素奠定了基础,并突出了与生育相关的基因作为维护生殖健康疗法的有希望的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/519d/12424747/7167a0ddee03/nihpp-2025.08.31.673173v2-f0007.jpg

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