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操纵信号通路以抑制宿主细胞凋亡。

: manipulation of signaling pathways to inhibit host cell apoptosis.

作者信息

Solano-Gálvez Sandra-Georgina, Álvarez-Hernández Diego-Abelardo, Gutiérrez-Kobeh Laila, Vázquez-López Rosalino

机构信息

Unidad de Investigación UNAM-INC, División Investigación, Facultad de Medicina, Universidad Nacional Autónoma de México, Instituto Nacional de Cardiología, Mexico City, Mexico.

Departamento de Microbiología, Centro de Investigación en Ciencias de la Salud, CICSA Facultad de Ciencias de la Salud, Universidad Anáhuac México Campus Norte, Huixquilucán Estado de México, México.

出版信息

Ther Adv Infect Dis. 2021 May 27;8:20499361211014977. doi: 10.1177/20499361211014977. eCollection 2021 Jan-Dec.

Abstract

The maintenance of homeostasis in living systems requires the elimination of unwanted cells which is performed, among other mechanisms, by type I cell death or apoptosis. This type of programmed cell death involves several morphological changes such as cytoplasm shrinkage, chromatin condensation (pyknosis), nuclear fragmentation (karyorrhexis), and plasma membrane blebbing that culminate with the formation of apoptotic bodies. In addition to the maintenance of homeostasis, apoptosis also represents an important defense mechanism for cells against intracellular microorganisms. In counterpart, diverse intracellular pathogens have developed a wide array of strategies to evade apoptosis and persist inside cells. These strategies include the manipulation of signaling pathways involved in the inhibition of apoptosis where mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K) play a key role. is an intracellular protozoan parasite that causes a wide spectrum of diseases known as leishmaniasis. This parasite displays different strategies, including apoptosis inhibition, to down-regulate host cell defense mechanisms in order to perpetuate infection.

摘要

生物系统中内环境稳态的维持需要清除不需要的细胞,这一过程通过多种机制实现,其中包括I型细胞死亡或凋亡。这种程序性细胞死亡涉及多种形态学变化,如细胞质收缩、染色质凝聚(核固缩)、核碎裂(核溶解)以及质膜起泡,最终形成凋亡小体。除了维持内环境稳态外,凋亡也是细胞抵御细胞内微生物的重要防御机制。相反,多种细胞内病原体已发展出一系列策略来逃避凋亡并在细胞内持续存在。这些策略包括操纵参与抑制凋亡的信号通路,其中丝裂原活化蛋白激酶(MAPK)和磷脂酰肌醇3激酶(PI3K)起关键作用。利什曼原虫是一种细胞内原生动物寄生虫,可引发一系列称为利什曼病的疾病。这种寄生虫表现出不同的策略,包括抑制凋亡,以下调宿主细胞防御机制,从而使感染持续存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee1/8165860/939a559681e3/10.1177_20499361211014977-fig1.jpg

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