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Fate of iPSCs derived from azoospermic and fertile men following Xenotransplantation to murine seminiferous tubules

机译:异精移植到小鼠生精小管后无精子和可育男人的iPSC的命运

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摘要

Historically, spontaneous deletions and insertions have provided means to probe germline developmental genetics in Drosophila, mouse and other species. Here, induced pluripotent stem cell (iPSC) lines were derived from infertile men with deletions that encompass three Y chromosome azoospermia factor (AZF) regions and are associated with production of few or no sperm but normal somatic development. AZF-deleted iPSC lines were compromised in germ cell development in vitro. Undifferentiated iPSCs transplanted directly into murine seminiferous tubules differentiated extensively to germ-cell-like cells (GCLCs) that localized near the basement membrane, demonstrated morphology indistinguishable from fetal germ cells, and expressed germ-cell-specific proteins diagnostic of primordial germ cells. Alternatively, all iPSCs that exited tubules formed primitive tumors. iPSCs with AZF deletions produced significantly fewer GCLCs in vivo with distinct defects in gene expression. Findings indicate that xenotransplantation of human iPSCs directs germ cell differentiation in a manner dependent on donor genetic status. © 2014 The Authors.
机译:从历史上看,自发的缺失和插入为探测果蝇,小鼠和其他物种的种系发育遗传学提供了手段。在这里,诱导多能干细胞(iPSC)系来自不育男性,其缺失包含三个Y染色体无精子因子(AZF)区,与精子的生成很少或没有,但体细胞发育正常。 AZF删除的iPSC系在体外生殖细胞发育中受到损害。未分化的iPSCs直接移植到鼠类生小管中,广泛分化为位于基底膜附近的生殖细胞样细胞(GCLC),表现出与胎儿生殖细胞无法区分的形态,并表达了生殖细胞特异性蛋白,可诊断原始生殖细胞。或者,所有退出肾小管的iPSC都形成原始肿瘤。具有AZF缺失的iPSC在体内产生的GCLC明显减少,且基因表达存在明显缺陷。研究结果表明,人类iPSC的异种移植以依赖供体遗传状态的方式指导生殖细胞分化。 ©2014作者。

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