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自噬在人类疾病中的作用:性别视角。

On the role of autophagy in human diseases: a gender perspective.

机构信息

Department of Therapeutic Research and Medicine Evaluation, Istituto Superiore di Sanitá, Viale Regina Elena 299, Rome, Italy.

出版信息

J Cell Mol Med. 2011 Jul;15(7):1443-57. doi: 10.1111/j.1582-4934.2011.01293.x.

DOI:10.1111/j.1582-4934.2011.01293.x
PMID:21362130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3823190/
Abstract

Cytopathological features of cells from males and females, i.e. XX and XY isolated cells, have been demonstrated to represent a key variable in the mechanism underlying gender disparity in human diseases. Major insights came from the studies of gender differences in cell fate, e.g. in apoptotic susceptibility. We report here some novel insights recently emerged from literature that are referred as to a cytoprotection mechanism by which cells recycle cytoplasm and dispose of excess or defective organelles, i.e. autophagy. Autophagy and related genes have first been identified in yeast. Orthologue genes have subsequently been found in other organisms, including human beings. This stimulated the research in the field and, thanks to the use of molecular genetics and cell biology in different model systems, autophagy gained the attention of several research groups operating to analyse the pathogenetic mechanisms of human diseases. It remains unclear, however, whether autophagy can exert a protective effect or instead contribute to the pathogenesis of important human diseases. On the basis of the growing importance of sex/gender as key determinant of human pathology and of the known differences between males and females in the onset, progression, drug susceptibility and outcome of a plethora of diseases, the idea that autophagy could represent key and critical factor should be taken into account. In the review, we summarize our current knowledge about the role of autophagy in some paradigmatic human diseases (cancer, neurodegenerative, autoimmune, cardiovascular) and the role of 'cell sex' differences in this context.

摘要

已证实,来自男性和女性(即 XX 和 XY 分离细胞)的细胞的细胞病理学特征是导致人类疾病性别差异的机制中的关键变量。主要的研究结果来自于对细胞命运(例如细胞凋亡易感性)的性别差异的研究。我们在此报告一些最近从文献中出现的新见解,这些见解被称为细胞保护机制,其中细胞回收细胞质并处理多余或有缺陷的细胞器,即自噬。自噬及其相关基因首先在酵母中被鉴定出来。随后在其他生物体中发现了同源基因,包括人类。这激发了该领域的研究,并且由于在不同模型系统中使用分子遗传学和细胞生物学,自噬引起了许多研究小组的关注,这些小组致力于分析人类疾病的发病机制。但是,自噬是否可以发挥保护作用,还是反而有助于许多重要人类疾病的发病机制,仍然不清楚。鉴于性别/性别作为人类病理学的关键决定因素的重要性日益增加,以及男性和女性在多种疾病的发病、进展、药物敏感性和结果方面的已知差异,应该考虑自噬可能代表关键和关键因素的想法。在综述中,我们总结了我们目前对自噬在一些典范人类疾病(癌症、神经退行性疾病、自身免疫性疾病、心血管疾病)中的作用以及“细胞性别”差异在这方面的作用的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/68f8f2b03f70/jcmm0015-1443-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/cf46e377466c/jcmm0015-1443-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/c2660dd38497/jcmm0015-1443-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/88173da8f43d/jcmm0015-1443-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/68f8f2b03f70/jcmm0015-1443-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/cf46e377466c/jcmm0015-1443-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/c2660dd38497/jcmm0015-1443-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/88173da8f43d/jcmm0015-1443-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b906/3823190/68f8f2b03f70/jcmm0015-1443-f4.jpg

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