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精子发生过程中的细胞因子与连接重组——从睾丸中获得的启示

Cytokines and junction restructuring during spermatogenesis--a lesson to learn from the testis.

作者信息

Xia Weiliang, Mruk Dolores D, Lee Will M, Cheng C Yan

机构信息

Population Council, Center for Biomedical Research, New York, NY 10021, USA.

出版信息

Cytokine Growth Factor Rev. 2005 Aug-Oct;16(4-5):469-93. doi: 10.1016/j.cytogfr.2005.05.007.

Abstract

In the mammalian testis, preleptotene and leptotene spermatocytes residing in the basal compartment of the seminiferous epithelium must traverse the blood-testis barrier (BTB) at late stage VIII through early stage IX of the epithelial cycle during spermatogenesis, entering the adluminal compartment for further development. However, until recently the regulatory mechanisms that regulate BTB dynamics remained largely unknown. We provide a critical review regarding the significance of cytokines in regulating the 'opening' and 'closing' of the BTB. We also discuss how cytokines may be working in concert with adaptors that selectively govern the downstream signaling pathways. This process, in turn, regulates the dynamics of either Sertoli-Sertoli tight junction (TJ), Sertoli-germ cell adherens junction (AJ), or both junction types in the epithelium, thereby permitting TJ opening without compromising AJs, and vice versa. We also discuss how adaptors alter their protein-protein association with the integral membrane proteins at the cell-cell interface via changes in their phosphorylation status, thereby altering adhesion function at AJ. These findings illustrate that the testis is a novel in vivo model to study the biology of junction restructuring. Furthermore, a molecular model is presented regarding how cytokines selectively regulate TJ/AJ restructuring in the epithelium during spermatogenesis.

摘要

在哺乳动物睾丸中,位于生精上皮基底室的前细线期和细线期精母细胞在精子发生过程中,必须在上皮周期的VIII期末至IX期初穿越血睾屏障(BTB),进入管腔间室以进一步发育。然而,直到最近,调节BTB动态变化的调控机制仍 largely未知。我们对细胞因子在调节BTB“开放”和“关闭”中的重要性进行了批判性综述。我们还讨论了细胞因子如何与选择性调控下游信号通路的衔接蛋白协同作用。反过来,这一过程调节了支持细胞-支持细胞紧密连接(TJ)、支持细胞-生殖细胞黏附连接(AJ)或上皮中这两种连接类型的动态变化,从而允许TJ开放而不损害AJ,反之亦然。我们还讨论了衔接蛋白如何通过其磷酸化状态的变化改变其在细胞-细胞界面与整合膜蛋白的蛋白质-蛋白质结合,从而改变AJ处的黏附功能。这些发现表明,睾丸是研究连接结构重组生物学的一种新型体内模型。此外,还提出了一个分子模型,阐述了细胞因子在精子发生过程中如何选择性调节上皮中的TJ/AJ重组。

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