Introductory Chapter: Spermatozoa - Facts and Perspectives

R. Chianese, R. Meccariello
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Abstract

Sperm cells (SPZ) are derived from spermatogenesis, a highly regulated developmental process starting from diploid precursors—spermatogonial stem cells—that undergo strictly orchestrated mitotic and meiotic divisions to form round spermatids. Extensive morphological and biochemical transformations in post-meiotic phase are required to differentiate round spermatids into highly specialized SPZ [1–3]. Thus, during spermiogenesis, the round spermatids transform into specialized and polarized cells that exhibit: at proximal end, the head containing an elongated and transcriptionally inactive nucleus which is apically surrounded by the Golgi-derived acrosome, and at the distal end, a tail surrounded at its proximal midpieces by mitochondrial sheet. A part from acrosome biogenesis, the spermiogenesis accounts for a radical chromatin remodeling that causes genome silencing [4] through histone replacement with transition proteins, firstly, and protamines later, to obtain a tightly packaged chromatin [5]. In parallel, a global reorganization of cytoplasmatic/cytoskeleton architecture drives elongation step with the development of a flagellum and the formation of cytoplasmic droplets which contain the excess cytoplasm.
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导论章:精子-事实和观点
精子细胞(SPZ)来源于精子发生,这是一个高度调控的发育过程,始于二倍体前体-精原干细胞-经过严格的有丝分裂和减数分裂形成圆形精子。圆形精子需要在减数分裂后发生广泛的形态和生化转变,才能分化为高度特化的SPZ[1-3]。因此,在精子发生过程中,圆形精子转变为特化和极化的细胞,其表现为:在近端,头部包含一个细长且转录活性的细胞核,其顶端被高尔基衍生顶体包围;在远端,尾巴在其近端中部被线粒体片包围。作为顶体生物发生的一部分,精子发生解释了染色质的自由基重塑,通过先用过渡蛋白取代组蛋白,然后再用精蛋白取代,从而导致基因组沉默[4],以获得紧密包装的染色质[5]。与此同时,细胞质/细胞骨架结构的整体重组推动了鞭毛的发育和包含多余细胞质的细胞质液滴的形成。
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