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细胞坏死性凋亡在发育和疾病中的作用。

Necroptosis in development and diseases.

机构信息

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, PuDong District, Shanghai 201203, China.

Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Genes Dev. 2018 Mar 1;32(5-6):327-340. doi: 10.1101/gad.312561.118.

Abstract

Necroptosis, a form of regulated necrotic cell death mediated by RIPK1 (receptor-interacting protein kinase 1) kinase activity, RIPK3, and MLKL (mixed-lineage kinase domain-like pseudokinase), can be activated under apoptosis-deficient conditions. Modulating the activation of RIPK1 by ubiquitination and phosphorylation is critical to control both necroptosis and apoptosis. Mutant mice with kinase-dead RIPK1 or RIPK3 and MLKL deficiency show no detrimental phenotype in regard to development and adult homeostasis. However, necroptosis and apoptosis can be activated in response to various mutations that result in the abortion of the defective embryos and human inflammatory and neurodegenerative pathologies. RIPK1 inhibition represents a key therapeutic strategy for treatment of diseases where blocking both necroptosis and apoptosis can be beneficial.

摘要

细胞坏死性凋亡是一种受 RIPK1(受体相互作用蛋白激酶 1)激酶活性、RIPK3 和 MLKL(混合谱系激酶结构域样假激酶)调节的程序性细胞坏死形式,可在凋亡缺陷条件下被激活。通过泛素化和磷酸化调节 RIPK1 的激活对于控制细胞坏死性凋亡和细胞凋亡至关重要。RIPK1 激酶失活或 RIPK3 和 MLKL 缺陷的突变小鼠在发育和成年期的稳态方面没有表现出有害表型。然而,细胞坏死性凋亡和细胞凋亡可以被各种导致缺陷胚胎流产和人类炎症及神经退行性病理的突变激活。RIPK1 抑制代表了一种治疗疾病的关键治疗策略,在这些疾病中,阻断细胞坏死性凋亡和细胞凋亡都可能是有益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea17/5900707/ae1c8c3ea5bc/327f01.jpg

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