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衰老及年龄相关性疾病中的小眼畸形相关转录因子

Microphthalmia-Associated Transcription Factor in Senescence and Age-Related Diseases.

作者信息

Zhang Jian, Mou Yi, Gong Hui, Chen Honghan, Xiao Hengyi

机构信息

Lab for Aging Research, National Clinical Research Center for Geriatrics, State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, China.

Geroscience and Chronic Disease Department, The 8th Municipal Hospital for the People, Chengdu, China.

出版信息

Gerontology. 2021;67(6):708-717. doi: 10.1159/000515525. Epub 2021 May 3.

Abstract

Although microphthalmia-associated transcription factor (MITF) has been known for decades as a key regulator for melanocytic differentiation, recent studies expanded its other roles in multiple biological processes. Among these newfound roles, the relationship between MITF and aging is attractive; however, the underlying mechanism remains elusive. Here, we review the documented cues that highlight the implication of MITF in the aging process and particularly discuss the possible mechanisms underlying the participation of MITF in cellular senescence. First, it summarizes the association of MITF with melanocytic senescence, including the roles of MITF in cell cycle regulation, DNA damage repair, oxidative stress response, and the generation of senescence-associated secretory phenotype. Then, it collects the information involving MITF-related senescent changes in nonmelanocytes, such as retinal pigment epithelium cells, osteoclasts, and cardiomyocytes. This review may deepen the understanding of MITF function and be helpful to develop new strategies for improving geriatric health.

摘要

尽管几十年来人们一直知道小眼畸形相关转录因子(MITF)是黑素细胞分化的关键调节因子,但最近的研究扩展了其在多个生物学过程中的其他作用。在这些新发现的作用中,MITF与衰老之间的关系很吸引人;然而,其潜在机制仍然难以捉摸。在这里,我们回顾了已记录的线索,这些线索突出了MITF在衰老过程中的作用,并特别讨论了MITF参与细胞衰老的可能机制。首先,总结了MITF与黑素细胞衰老的关联,包括MITF在细胞周期调控、DNA损伤修复、氧化应激反应以及衰老相关分泌表型产生中的作用。然后,收集了涉及非黑素细胞(如视网膜色素上皮细胞、破骨细胞和心肌细胞)中与MITF相关的衰老变化的信息。这篇综述可能会加深对MITF功能的理解,并有助于制定改善老年健康的新策略。

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