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鉴定ABHD6为哺乳动物肝脏和肾脏中的溶血磷脂酰丝氨酸脂肪酶。

Identification of ABHD6 as a lysophosphatidylserine lipase in the mammalian liver and kidneys.

作者信息

Chakraborty Arnab, Punnamraju Prajwal, Sajeevan Theja, Kaur Arshdeep, Kolthur-Seetharam Ullas, Kamat Siddhesh S

机构信息

Department of Biology, Indian Institute of Science Education and Research, Pune, Maharashtra, India.

Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra, India.

出版信息

J Biol Chem. 2025 Feb;301(2):108157. doi: 10.1016/j.jbc.2025.108157. Epub 2025 Jan 4.

DOI:10.1016/j.jbc.2025.108157
PMID:39761854
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11808726/
Abstract

Lysophosphatidylserine (lyso-PS) is a potent hormone-like signaling lysophospholipid, which regulates many facets of mammalian biology and dysregulation in its metabolism is associated with several human neurological and autoimmune diseases. Despite the physiological importance and causal relation with human pathophysiology, little is known about the metabolism of lyso-PS in tissues other than the nervous and immune systems. To address this problem, here, we attempted to identify one (or more) lipase(s) capable of degrading lyso-PS in different mammalian tissues. We found that the membrane fraction of most mammalian tissues possess lyso-PS lipase activity, yet interestingly, the only bona fide lyso-PS lipase ABHD12 displays this enzymatic activity and has control over lyso-PS metabolism only in the mammalian brain. Using an in vitro inhibitor screen against membrane fractions of different tissues, we find that another lipase from the metabolic serine hydrolase family, ABHD6, is a putative lyso-PS lipase in the mouse liver and kidney. Finally, using pharmacological tools, we validate the lyso-PS lipase activity of ABHD6 in vivo, and functionally designate this enzyme as a major lyso-PS lipase in primary hepatocytes, and the mammalian liver and kidneys.

摘要

溶血磷脂酰丝氨酸(lyso-PS)是一种具有强大激素样信号作用的溶血磷脂,它调节着哺乳动物生物学的许多方面,其代谢失调与多种人类神经和自身免疫性疾病相关。尽管lyso-PS在生理上具有重要意义且与人类病理生理学存在因果关系,但除神经和免疫系统外,人们对其在其他组织中的代谢知之甚少。为了解决这个问题,我们在此尝试鉴定一种(或多种)能够在不同哺乳动物组织中降解lyso-PS的脂肪酶。我们发现大多数哺乳动物组织的膜部分具有lyso-PS脂肪酶活性,但有趣的是,唯一真正的lyso-PS脂肪酶ABHD12仅在哺乳动物大脑中显示出这种酶活性并控制lyso-PS的代谢。通过针对不同组织膜部分的体外抑制剂筛选,我们发现代谢丝氨酸水解酶家族的另一种脂肪酶ABHD6是小鼠肝脏和肾脏中一种假定的lyso-PS脂肪酶。最后,我们使用药理学工具在体内验证了ABHD6的lyso-PS脂肪酶活性,并在功能上将该酶指定为原代肝细胞以及哺乳动物肝脏和肾脏中的主要lyso-PS脂肪酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/50b18cedf10a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/bd5e002252e4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/34474dfdb5f9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/7fd9ddec451f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/d0319737e1cb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/4b01b29ac0fb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/498a9b8b3d4f/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/50b18cedf10a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/bd5e002252e4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/34474dfdb5f9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/7fd9ddec451f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/d0319737e1cb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/4b01b29ac0fb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/498a9b8b3d4f/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6428/11808726/50b18cedf10a/gr7.jpg

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