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自噬和细胞凋亡作为伴侣在热应激后诱导小鼠生殖细胞死亡。

Autophagy and apoptosis act as partners to induce germ cell death after heat stress in mice.

机构信息

State Key Laboratory of Reproductive Medicine, Department of Histology and Embryology, Nanjing Medical University, Nanjing, Jiangsu Province, China.

出版信息

PLoS One. 2012;7(7):e41412. doi: 10.1371/journal.pone.0041412. Epub 2012 Jul 25.

Abstract

Testicular heating suppresses spermatogenesis which is marked by germ cell loss via apoptotic pathways. Recently, it is reported that autophagy also can be induced by heat treatment in somatic cells. In this study, the status of autophagy in germ cells after heat treatment, as well as the partnership between autophagy and apoptosis in these cells was investigated. The results demonstrated that besides initiating apoptotic pathways, heat also induced autophagic pathways in germ cells. Exposure of germ cells to hyperthermia resulted in several specific features of the autophagic process, including autophagosome formation and the conversion of LC3-I to LC3-II. Furthermore, the ubiquitin-like protein conjugation system was implicated as being likely responsible for heat-induced autophagy in germ cells since all genes involving this system were found to be expressed in the testes. In addition, the upstream protein in this system, Atg7 (Autophagy-related gene 7), was found to be expressed in all types of spermatogenic cells, and its expression level was positively correlated with the level of autophagy in germ cells. As a result, Atg7 was selected as the investigative target to further analyze the role of autophagy in heat-induced germ cell death. It was shown that down expression of Atg7 protein resulted in the notable decrease in the level of autophagy in heat-treated germ cells, and this down-regulation of autophagy caused by Atg7 knockdown further reduced the apoptotic rate of germ cells. These results suggest that autophagy plays a positive role in the process of germ cell apoptosis after heat treatment. In conclusion, this study demonstrates that heat triggers autophagy and apoptosis in germ cells. These two mechanisms might act as partners, not antagonist, to induce cell death and lead to eventual destruction of spermatogenesis.

摘要

睾丸加热会抑制生精作用,这标志着生殖细胞通过凋亡途径丢失。最近有报道称,热疗也可以诱导体细胞发生自噬。在这项研究中,研究了热处理后生殖细胞中自噬的状态,以及自噬和这些细胞中凋亡之间的关系。结果表明,热除了引发凋亡途径外,还会诱导生殖细胞发生自噬途径。生殖细胞暴露于高温会导致自噬过程的几个特定特征,包括自噬体的形成和 LC3-I 向 LC3-II 的转化。此外,泛素样蛋白连接系统可能是导致生殖细胞热诱导自噬的原因,因为该系统涉及的所有基因都在睾丸中表达。此外,该系统的上游蛋白 Atg7(自噬相关基因 7)在所有类型的生精细胞中都有表达,其表达水平与生殖细胞自噬水平呈正相关。因此,选择 Atg7 作为研究对象,进一步分析自噬在热诱导生殖细胞死亡中的作用。结果表明,Atg7 蛋白表达下调导致热处理后生殖细胞自噬水平明显下降,Atg7 敲低引起的自噬下调进一步降低了生殖细胞的凋亡率。这些结果表明自噬在热处理后生殖细胞凋亡过程中发挥积极作用。总之,这项研究表明,热会引发生殖细胞的自噬和凋亡。这两种机制可能作为伙伴,而不是拮抗剂,诱导细胞死亡并最终导致生精作用的破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d1/3405141/c8f522f728cb/pone.0041412.g001.jpg

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