Literature DB >> 28939644

Role of lysophosphatidic acid and its receptors in the kidney.

Frank Park1, Duane D Miller2.   

Abstract

Lysophosphatidic acid (LPA) is a bioactive phospholipid that can exert diverse biological effects in various diseased states of the kidney by activating at least six cognate G protein-coupled receptors and its complex network of heterotrimeric G proteins. In many models of acute and chronic kidney injury, pathological elevations in LPA promotes abnormal changes in renal tubular epithelial cell architecture by activating apoptotic signaling, recruits immune cells to the site of injury, and stimulates profibrotic signaling by increasing gene transcription. In renal cancers, LPA can promote vascular cell proliferation and tumor cell invasion. In this review, a summary will be provided to describe the involvement of LPA, its synthetic enzymes, and its associated receptors in normal and diseased kidneys. Further elucidation of the LPA system may open new doors in developing a lipid-receptor therapeutic platform for kidney diseases.
Copyright © 2017 the American Physiological Society.

Entities:  

Keywords:  G protein-coupled receptors; acute kidney injury; autotaxin; chronic kidney disease; kidney; lysophosphatidic acid; phospholipids

Mesh:

Substances:

Year:  2017        PMID: 28939644     DOI: 10.1152/physiolgenomics.00070.2017

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  8 in total

1.  Lysophosphatidic acid (LPA) as a modulator of plasma membrane Ca2+-ATPase from basolateral membranes of kidney proximal tubules.

Authors:  Julliana F Sant'Anna; Vanessa S Baldez; Natalie A Razuck-Garrão; Thiago Lemos; Bruno L Diaz; Marcelo Einicker-Lamas
Journal:  J Physiol Biochem       Date:  2021-03-11       Impact factor: 4.158

2.  Admission Lysophosphatidic Acid Is Related to Impaired Kidney Function in Acute Aortic Dissection: 2-Year Retrospective Follow-Up Study.

Authors:  Xiaogao Pan; Guifang Yang; Ning Ding; Wen Peng; Tuo Guo; Mengping Zeng; Xiangping Chai
Journal:  Front Cardiovasc Med       Date:  2022-06-16

3.  Loss of Arhgef11 in the Dahl Salt-Sensitive Rat Protects Against Hypertension-Induced Renal Injury.

Authors:  Ashley C Johnson; Wenjie Wu; Esinam M Attipoe; Jennifer M Sasser; Erin B Taylor; Kurt C Showmaker; Patrick B Kyle; Merry L Lindsey; Michael R Garrett
Journal:  Hypertension       Date:  2020-03-09       Impact factor: 10.190

4.  Cooperative activation of divergent pathways by LPAR1 and LPAR2 receptors in fibrotic signaling.

Authors:  Marpadga A Reddy; Rama Natarajan
Journal:  Am J Physiol Renal Physiol       Date:  2021-01-25

Review 5.  Lipid Signaling in Ocular Neovascularization.

Authors:  Ryo Terao; Hiroki Kaneko
Journal:  Int J Mol Sci       Date:  2020-07-04       Impact factor: 5.923

6.  The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos.

Authors:  Karine Massé; Surinder Bhamra; Christian Paroissin; Lilly Maneta-Peyret; Eric Boué-Grabot; Elizabeth A Jones
Journal:  Commun Biol       Date:  2021-10-07

7.  Inhibition of ChREBP ubiquitination via the ROS/Akt-dependent downregulation of Smurf2 contributes to lysophosphatidic acid-induced fibrosis in renal mesangial cells.

Authors:  Donghee Kim; Ga-Young Nam; Eunhui Seo; Hee-Sook Jun
Journal:  J Biomed Sci       Date:  2022-05-10       Impact factor: 12.771

8.  Effect of BBT-877, a novel inhibitor of ATX, on a mouse model of type 1 diabetic nephropathy.

Authors:  Jong Han Lee; Phyu Phyu Khin; GwangHee Lee; Oh Kyung Lim; Hee-Sook Jun
Journal:  Aging (Albany NY)       Date:  2022-08-26       Impact factor: 5.955

  8 in total

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