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分泌型磷脂酶 A2 酶的新作用:转基因和基因敲除小鼠的启示。

Emerging roles of secreted phospholipase A2 enzymes: Lessons from transgenic and knockout mice.

机构信息

Biomembrane Signaling Project, The Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.

出版信息

Biochimie. 2010 Jun;92(6):561-82. doi: 10.1016/j.biochi.2010.03.015. Epub 2010 Mar 27.

Abstract

Among the emerging phospholipase A(2) (PLA(2)) superfamily, the secreted PLA(2) (sPLA(2)) family consists of low-molecular-mass, Ca(2+)-requiring extracellular enzymes with a His-Asp catalytic dyad. To date, more than 10 sPLA(2) enzymes have been identified in mammals. Individual sPLA(2)s exhibit unique tissue and cellular localizations and enzymatic properties, suggesting their distinct pathophysiological roles. Despite numerous enzymatic and cell biological studies on this enzyme family in the past two decades, their precise in vivo functions still remain largely obscure. Recent studies using transgenic and knockout mice for several sPLA(2) enzymes, in combination with lipidomics approaches, have opened new insights into their distinct contributions to various biological events such as food digestion, host defense, inflammation, asthma and atherosclerosis. In this article, we overview the latest understanding of the pathophysiological functions of individual sPLA(2) isoforms fueled by studies employing transgenic and knockout mice for several sPLA(2)s.

摘要

在新出现的磷脂酶 A(2)(PLA(2))超家族中,分泌型 PLA(2)(sPLA(2))家族由低分子量、需要 Ca(2+)的细胞外酶组成,具有 His-Asp 催化二联体。迄今为止,哺乳动物中已经鉴定出超过 10 种 sPLA(2)酶。单个 sPLA(2)表现出独特的组织和细胞定位以及酶学特性,表明它们具有不同的病理生理作用。尽管在过去的二十年中对该酶家族进行了大量的酶学和细胞生物学研究,但它们的确切体内功能仍然很大程度上不清楚。最近使用几种 sPLA(2)酶的转基因和基因敲除小鼠结合脂质组学方法的研究为它们在食物消化、宿主防御、炎症、哮喘和动脉粥样硬化等各种生物学事件中的独特贡献提供了新的见解。本文综述了利用几种 sPLA(2)酶的转基因和基因敲除小鼠进行研究,对个体 sPLA(2)同工型的病理生理功能的最新认识。

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