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溶血磷脂酸(LPA)受体3介导的LPA信号转导途径:与植入前猪胚胎早期发育的可能关系。

Lysophosphatidic Acid (LPA) Receptor 3-Mediated LPA Signal Transduction Pathways: A Possible Relationship with Early Development of Peri-Implantation Porcine Conceptus.

作者信息

Jeong Wooyoung, Seo Heewon, Sung Yujin, Ka Hakhyun, Song Gwonhwa, Kim Jinyoung

机构信息

Department of Animal Resources Science, Dankook University, Cheonan, Republic of Korea.

Division of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.

出版信息

Biol Reprod. 2016 May;94(5):104. doi: 10.1095/biolreprod.115.137174. Epub 2016 Mar 30.

Abstract

Lysophosphatidic acid (LPA) is a phospholipid with a variety of fatty acyl groups that mediates diverse biological effects on various types of cells through specific G protein-coupled receptors. LPA appears to play a significant role in many reproductive processes, including luteolysis, implantation, and placentation. Our previous study in pigs demonstrated that LPA and the LPA receptor system are present at the maternal-conceptus interface and that LPA increases uterine endometrial expression of prostaglandin-endoperoxide synthase 2 (PTGS2) through LPA receptor 3 (LPAR3). However, the role of LPA in conceptuses during early pregnancy has not been determined. Therefore, this study examined the effects of LPA in cell proliferation, migration, and activation of the intracellular signaling pathway in porcine conceptuses by using an established porcine trophectoderm (pTr) cell line isolated from Day 12 conceptuses. All examined LPA species with various fatty acid lengths increased proliferation and migration of pTr cells as the dosage increased. Immunoblot analyses found that LPA activated intracellular signaling molecules, extracellular signal-regulated kinase 1/2 (ERK1/2), ribosomal protein S6 kinase 90 kDa (P90RSK), ribosomal protein S6 (RPS6), and P38 in pTr cells. Furthermore, LPA increased expression of PTGS2 and urokinase-type plasminogen activator (PLAU), and the LPA-induced increases in PTGS2 and PLAU expression were inhibited by LPAR3 siRNA. Collectively, these results showed that LPA promotes proliferation, migration, and differentiation of pTr cells by activating the ERK1/2-P90RSK-RPS6 and P38 pathways, indicating that the LPA-LPAR3 system may be involved in the development of trophoblast during early pregnancy in pigs.

摘要

溶血磷脂酸(LPA)是一种含有多种脂肪酰基的磷脂,它通过特定的G蛋白偶联受体介导对各种类型细胞的多种生物学效应。LPA似乎在许多生殖过程中发挥重要作用,包括黄体溶解、着床和胎盘形成。我们之前在猪身上的研究表明,LPA和LPA受体系统存在于母体-孕体界面,并且LPA通过LPA受体3(LPAR3)增加前列腺素内过氧化物合酶2(PTGS2)的子宫内膜表达。然而,LPA在妊娠早期孕体中的作用尚未确定。因此,本研究通过使用从第12天孕体分离的成熟猪滋养外胚层(pTr)细胞系,研究了LPA对猪孕体细胞增殖、迁移和细胞内信号通路激活的影响。随着剂量增加,所有检测的具有不同脂肪酸长度的LPA种类均增加了pTr细胞的增殖和迁移。免疫印迹分析发现,LPA激活了pTr细胞中的细胞内信号分子,细胞外信号调节激酶1/2(ERK1/2)、核糖体蛋白S6激酶90 kDa(P90RSK)、核糖体蛋白S6(RPS6)和P38。此外,LPA增加了PTGS2和尿激酶型纤溶酶原激活剂(PLAU)的表达,并且LPAR3 siRNA抑制了LPA诱导的PTGS2和PLAU表达增加。总体而言,这些结果表明,LPA通过激活ERK1/2-P90RSK-RPS6和P38途径促进pTr细胞的增殖、迁移和分化,表明LPA-LPAR3系统可能参与猪妊娠早期滋养层的发育。

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