Lysophospholipase D activity on oral mucosa cells in whole mixed human saliva involves in production of bioactive lysophosphatidic acid from lysophosphatidylcholine

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Prostaglandins & other lipid mediators Pub Date : 2024-08-10 DOI:10.1016/j.prostaglandins.2024.106881
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Abstract

We reported that lysophosphatidic acid (LPA) is present at 0.8 μM in mixed human saliva (MS). In this study, we examined the distribution, origin, and enzymatic generation pathways of LPA in MS. LPA was distributed in the medium and cell pellet fraction; a true level of soluble LPA in MS was about 150 nM. The soluble LPA was assumed to be generated by ecto-type lysophospholipase D on exfoliated cells in MS from LPC that originated mainly from the major salivary gland saliva. Our results with the albumin-back extraction procedures suggest that a significant pool of LPA is kept in the outer layer of the plasma membranes of detached oral mucosal cells. Such pool of LPA may contribute to wound healing in upper digestive organs including oral cavity. We obtained evidence that the choline-producing activity in MS was mainly due to Ca2+-activated lysophospholipase D activity of glycerophosphodiesterase 7.

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全混合人类唾液中口腔黏膜细胞上的溶血磷脂酶 D 活性涉及从溶血磷脂酰胆碱中生成生物活性溶血磷脂酸。
我们曾报道,溶血磷脂酸(LPA)在混合人类唾液(MS)中的含量为 0.8 μM。本研究考察了 LPA 在 MS 中的分布、来源和酶生成途径。LPA 分布在培养基和细胞颗粒部分;MS 中可溶性 LPA 的真实水平约为 150nM。假定可溶性 LPA 是由 MS 中脱落细胞上的外型溶血磷脂酶 D 从主要来源于唾液腺唾液的 LPC 生成的。我们使用白蛋白后提取程序得出的结果表明,在脱落的口腔黏膜细胞的质膜外层保存着大量的 LPA。这种 LPA 池可能有助于包括口腔在内的上消化道器官的伤口愈合。我们获得的证据表明,MS中产生胆碱的活性主要是由于甘油磷酸二酯酶7的Ca2+激活溶血磷脂酶D的活性(148个字)。
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来源期刊
Prostaglandins & other lipid mediators
Prostaglandins & other lipid mediators 生物-生化与分子生物学
CiteScore
5.80
自引率
3.40%
发文量
49
审稿时长
2 months
期刊介绍: Prostaglandins & Other Lipid Mediators is the original and foremost journal dealing with prostaglandins and related lipid mediator substances. It includes basic and clinical studies related to the pharmacology, physiology, pathology and biochemistry of lipid mediators. Prostaglandins & Other Lipid Mediators invites reports of original research, mini-reviews, reviews, and methods articles in the basic and clinical aspects of all areas of lipid mediator research: cell biology, developmental biology, genetics, molecular biology, chemistry, biochemistry, physiology, pharmacology, endocrinology, biology, the medical sciences, and epidemiology. Prostaglandins & Other Lipid Mediators also accepts proposals for special issue topics. The Editors will make every effort to advise authors of the decision on the submitted manuscript within 3-4 weeks of receipt.
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