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细胞质磷脂酶 A2 作为疾病发病机制的介质。

Cytosolic phospholipase A2 as a mediator of disease pathogenesis.

机构信息

Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Cell Microbiol. 2010 Oct;12(10):1369-77. doi: 10.1111/j.1462-5822.2010.01505.x.

Abstract

As efficient catalysts, enzymes help maintain a variety of biological and chemical transformations necessary for cellular metabolism and normal physiology. Unfortunately, pathogenic microbes can also exploit enzymatic reactions in an attempt to spread infection. Cytosolic phospholipase A2 (cPLA(2) ) is an enzyme that is responsible for the hydrolysis of membrane phospholipids such as phosphatidylcholine. Following activation, cPLA(2) cleaves phosphatidylcholine to yield free fatty acid and lysophosphatidylcholine. Both of these products and their downstream metabolites initiate a network of signalling cascades that influence cellular viability and inflammation. Recent observations have shown that viral and bacterial agents often target this intricate organization of signalling molecules. This review briefly discusses the role of cPLA(2) in the biological response to disease-causing pathogens and injury, the immunological process and tumour progression.

摘要

作为高效的催化剂,酶有助于维持细胞代谢和正常生理所需的各种生物和化学反应。不幸的是,致病微生物也可以利用酶反应来试图传播感染。细胞质磷脂酶 A2(cPLA2)是一种负责水解膜磷脂如磷脂酰胆碱的酶。激活后,cPLA2 裂解磷脂酰胆碱生成游离脂肪酸和溶血磷脂酰胆碱。这些产物及其下游代谢物启动了一系列信号级联反应,影响细胞活力和炎症。最近的观察表明,病毒和细菌通常针对这种复杂的信号分子组织。本综述简要讨论了 cPLA2 在对致病病原体和损伤的生物学反应、免疫过程和肿瘤进展中的作用。

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