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DNA损伤反应与免疫防御:联系与机制

DNA Damage Response and Immune Defense: Links and Mechanisms.

作者信息

Nakad Rania, Schumacher Björn

机构信息

Institute for Genome Stability in Ageing and Disease, Medical Faculty, University of CologneCologne, Germany; Cologne Excellence Cluster for Cellular Stress Responses in Aging-Associated Diseases, Center for Molecular Medicine Cologne and Systems Biology of Ageing Cologne, University of CologneCologne, Germany.

出版信息

Front Genet. 2016 Aug 9;7:147. doi: 10.3389/fgene.2016.00147. eCollection 2016.

Abstract

DNA damage plays a causal role in numerous human pathologies including cancer, premature aging, and chronic inflammatory conditions. In response to genotoxic insults, the DNA damage response (DDR) orchestrates DNA damage checkpoint activation and facilitates the removal of DNA lesions. The DDR can also arouse the immune system by for example inducing the expression of antimicrobial peptides as well as ligands for receptors found on immune cells. The activation of immune signaling is triggered by different components of the DDR including DNA damage sensors, transducer kinases, and effectors. In this review, we describe recent advances on the understanding of the role of DDR in activating immune signaling. We highlight evidence gained into (i) which molecular and cellular pathways of DDR activate immune signaling, (ii) how DNA damage drives chronic inflammation, and (iii) how chronic inflammation causes DNA damage and pathology in humans.

摘要

DNA损伤在包括癌症、早衰和慢性炎症性疾病在内的众多人类疾病中起着因果作用。作为对基因毒性损伤的反应,DNA损伤反应(DDR)协调DNA损伤检查点的激活,并促进DNA损伤的清除。DDR还可以通过例如诱导抗菌肽以及免疫细胞上发现的受体配体的表达来激活免疫系统。免疫信号的激活由DDR的不同组分触发,包括DNA损伤传感器、转导激酶和效应器。在本综述中,我们描述了在理解DDR在激活免疫信号中的作用方面的最新进展。我们重点介绍了以下方面的证据:(i)DDR的哪些分子和细胞途径激活免疫信号,(ii)DNA损伤如何驱动慢性炎症,以及(iii)慢性炎症如何导致人类DNA损伤和疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca62/4977279/50bcf364d1b6/fgene-07-00147-g001.jpg

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