mPGES-1-Derived PGE2 Contributes to Indoxyl Sulfate-Induced Mesangial Cell Proliferation
Author(s) -
Shuzhen Li,
Zhenzhen Sun,
Guixia Ding,
Wei Gong,
Jing Yu,
Weiwei Xia,
Songming Huang,
Aihua Zhang,
Yue Zhang,
Zhanjun Jia
Publication year - 2017
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000480369
Subject(s) - downregulation and upregulation , cell growth , cyclin d1 , prostaglandin e2 , prostaglandin e2 receptor , prostaglandin e , chemistry , gene silencing , prostaglandin , cyclooxygenase , cell cycle , microbiology and biotechnology , cancer research , apoptosis , receptor , endocrinology , medicine , biology , biochemistry , enzyme , gene , agonist
We previously reported that indoxyl sulfate (IS) could cause mesangial cell (MC) proliferation via a cyclooxygenase (COX)-2-dependent mechanism. However, the specific prostaglandin contributing to COX-2 effect on IS-induced MC proliferation remained unknown. Thus, the present study was undertaken to examine the role of microsomal prostaglandin E synthase-1 (mPGES-1)-derived Prostaglandin E2 (PGE2) in IS-induced MC proliferation.
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