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Id蛋白在雄性生殖细胞和支持细胞中的阶段及亚细胞特异性表达表明,Id蛋白在减数分裂、精子发生和支持细胞功能过程中具有独特的调节作用。

Stage- and subcellular-specific expression of Id proteins in male germ and Sertoli cells implicates distinctive regulatory roles for Id proteins during meiosis, spermatogenesis, and Sertoli cell function.

作者信息

Sablitzky F, Moore A, Bromley M, Deed R W, Newton J S, Norton J D

机构信息

Department of Medicine, The Windeyer Institute of Medical Sciences, University College London, United Kingdom.

出版信息

Cell Growth Differ. 1998 Dec;9(12):1015-24.

PMID:9869302
Abstract

Immunohistological detection of each of the four Id proteins (Id1-Id4) in sections of mouse testis revealed a unique temporal and spatial expression pattern for each Id protein during spermatogenesis. Furthermore, each Id protein displayed a distinctive, dynamic pattern of subcellular distribution. Id1 was uniquely expressed in MI/MII spermatocytes undergoing meiotic division. Id4 protein was detectable in the cytoplasm of type A1 spermatogonia, as well as in late pachytene and in diplotene spermatocytes. Id2 protein, which was most abundant in Sertoli cell nuclei, was also detectable in pachytene and diplotene spermatocytes, but as with Id4, it was absent from MI/MII cells. In postmeiotic spermatids, Id1, Id2, and Id4 proteins were expressed in a stage- and subcellular-specific manner. Expression of Id3 was restricted to Sertoli cell cytoplasm. In malignant seminoma cells, all four Id proteins were abundantly expressed with accompanying changes in their subcellular distribution. The observed expression of Id proteins in postproliferative Sertoli cells and spermatids and during specific stages of meiosis implies novel functional roles for this class of transcriptional regulator during spermatogenesis.

摘要

对小鼠睾丸切片中四种Id蛋白(Id1-Id4)进行免疫组织学检测,结果显示,在精子发生过程中,每种Id蛋白都有独特的时空表达模式。此外,每种Id蛋白都呈现出独特的、动态的亚细胞分布模式。Id1在进行减数分裂的MI/MII精母细胞中独特表达。Id4蛋白在A1型精原细胞的细胞质中可检测到,在粗线期晚期和双线期精母细胞中也可检测到。Id2蛋白在支持细胞核中含量最多,在粗线期和双线期精母细胞中也可检测到,但与Id4一样,在MI/MII细胞中不存在。在减数分裂后的精子细胞中,Id1、Id2和Id4蛋白以阶段和亚细胞特异性方式表达。Id3的表达局限于支持细胞的细胞质中。在恶性精原细胞瘤细胞中,所有四种Id蛋白均大量表达,且亚细胞分布伴随变化。在增殖后的支持细胞和精子细胞以及减数分裂的特定阶段观察到的Id蛋白表达,意味着这类转录调节因子在精子发生过程中具有新的功能作用。

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