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细胞黏附与免疫应答,两种主要功能在两种哺乳动物季节性退化睾丸转录组中发生改变。

Cell adhesion and immune response, two main functions altered in the transcriptome of seasonally regressed testes of two mammalian species.

机构信息

Departamento de Genética e Instituto de Biotecnología, Lab. 127, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.

RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.

出版信息

J Exp Zool B Mol Dev Evol. 2023 May;340(3):231-244. doi: 10.1002/jez.b.23142. Epub 2022 May 10.

Abstract

In species with seasonal breeding, male specimens undergo substantial testicular regression during the nonbreeding period of the year. However, the molecular mechanisms that control this biological process are largely unknown. Here, we report a transcriptomic analysis on the Iberian mole, Talpa occidentalis, in which the desquamation of live, nonapoptotic germ cells is the major cellular event responsible for testis regression. By comparing testes at different reproductive states (active, regressing, and inactive), we demonstrate that the molecular pathways controlling the cell adhesion function in the seminiferous epithelium, such as the MAPK, ERK, and TGF-β signaling, are altered during the regression process. In addition, inactive testes display a global upregulation of genes associated with immune response, indicating a selective loss of the "immune privilege" that normally operates in sexually active testes. Interspecies comparative analyses using analogous data from the Mediterranean pine vole, a rodent species where testis regression is controlled by halting meiosis entry, revealed a common gene expression signature in the regressed testes of these two evolutionary distant species. Our study advances in the knowledge of the molecular mechanisms associated to gonadal seasonal breeding, highlighting the existence of a conserved transcriptional program of testis involution across mammalian clades.

摘要

在具有季节性繁殖的物种中,雄性个体在一年的非繁殖期会经历显著的睾丸退化。然而,控制这一生物学过程的分子机制在很大程度上尚不清楚。在这里,我们对伊比利亚鼹鼠(Talpa occidentalis)进行了转录组分析,在该物种中,活的、非凋亡性生殖细胞的脱落是导致睾丸退化的主要细胞事件。通过比较不同生殖状态(活跃、退化和不活跃)的睾丸,我们证明了控制精小管上皮细胞黏附功能的分子途径,如 MAPK、ERK 和 TGF-β 信号通路,在退化过程中发生了改变。此外,不活跃的睾丸显示出与免疫反应相关的基因的全面上调,表明正常在活跃睾丸中起作用的“免疫特权”发生了选择性丧失。使用来自地中海滨鼠(一种由停止减数分裂进入控制睾丸退化的啮齿动物物种)的类似数据进行的种间比较分析,揭示了这两个进化上相距甚远的物种退化睾丸中存在共同的基因表达特征。我们的研究增进了对与性腺季节性繁殖相关的分子机制的认识,突出了在哺乳动物进化枝中存在保守的睾丸退化转录程序。

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