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细胞破坏:蛋白质作为细胞程序性死亡的分子参与者。

Cellular demolition: Proteins as molecular players of programmed cell death.

机构信息

Developmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research (CSIR-IITR), Vishvigyan Bhawan, 31, Mahatma Gandhi Marg, Lucknow 226 001, India.

Department of Biochemistry, National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Tajganj, Agra, India; Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India.

出版信息

Int J Biol Macromol. 2019 Oct 1;138:492-503. doi: 10.1016/j.ijbiomac.2019.07.113. Epub 2019 Jul 19.

Abstract

Apoptosis, a well-characterized and regulated cell death programme in eukaryotes plays a fundamental role in developing or later-life periods to dispose of unwanted cells to maintain typical tissue architecture, homeostasis in a spatiotemporal manner. This silent cellular death occurs without affecting any neighboring cells/tissue and avoids triggering of immunological response. Furthermore, diminished forms of apoptosis result in cancer and autoimmune diseases, whereas unregulated apoptosis may also lead to the development of a myriad of neurodegenerative diseases. Unraveling the mechanistic events in depth will provide new insights into understanding physiological control of apoptosis, pathological consequences of abnormal apoptosis and development of novel therapeutics for diseases. Here we provide a brief overview of molecular players of programmed cell death with discussion on the role of caspases, modifications, ubiquitylation in apoptosis, removal of the apoptotic body and its relevance to diseases.

摘要

细胞凋亡是真核生物中一种特征明确且受到调控的细胞死亡程序,在发育或生命后期发挥着重要作用,通过清除不需要的细胞来维持组织的正常结构和时空内的内稳态。这种静默的细胞死亡不会影响邻近的细胞/组织,也不会引发免疫反应。此外,凋亡程度降低会导致癌症和自身免疫性疾病,而不受调控的凋亡也可能导致多种神经退行性疾病的发生。深入研究这些机制事件将为理解凋亡的生理控制、异常凋亡的病理后果以及疾病的新型治疗方法提供新的见解。在这里,我们简要概述了程序性细胞死亡的分子参与者,并讨论了半胱天冬酶、修饰、泛素化在凋亡中的作用、凋亡小体的清除及其与疾病的相关性。

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