Department of Pharmaceutical Sciences, Kyushu University of Medical Science, Nobeoka 882-8508, Japan.
Department of Pharmaceutical Health Chemistry, Graduate School of Biomedical Sciences, Tokushima University, Shomachi, Tokushima 770-8505, Japan.
Prostaglandins Other Lipid Mediat. 2024 Oct;174:106881. doi: 10.1016/j.prostaglandins.2024.106881. Epub 2024 Aug 10.
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 Ca-activated lysophospholipase D activity of glycerophosphodiesterase 7.
我们曾报道,混合唾液(MS)中的溶血磷脂酸(LPA)浓度为 0.8 μM。在本研究中,我们对 MS 中 LPA 的分布、来源和酶促生成途径进行了研究。LPA 分布于中相和细胞沉淀相;MS 中可溶性 LPA 的真实水平约为 150 nM。推测 MS 中可溶性 LPA 是由脱落细胞表面的ecto 型溶血磷脂酶 D 从主要来源于大唾液腺唾液的 LPC 生成的。我们通过白蛋白反萃取程序获得的结果表明,在脱落的口腔黏膜细胞的质膜外层存在大量的 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 中的胆碱产生活性主要归因于甘油磷酸二酯酶 7 的 Ca 激活型溶血磷脂酶 D 活性。