Literature DB >> 17064959

Expression of mouse membrane-associated prostaglandin E2 synthase-2 (mPGES-2) along the urogenital tract.

Guangrui Yang1, Lihong Chen, Yahua Zhang, Xiaoyan Zhang, Jing Wu, Shuo Li, Mingfen Wei, Zhiwen Zhang, Matthew D Breyer, Youfei Guan.   

Abstract

Prostaglandin E(2) (PGE(2)) is the most common prostanoid and has a variety of bioactivities including a crucial role in urogenital function. Multiple enzymes are involved in its biosynthesis. Among 3 PGE(2) terminal synthetic enzymes, membrane-associated PGE(2) synthase-2 (mPGES-2) is the most recently identified, and its role remains uncharacterized. In previous studies, membrane-associated PGE(2) synthase-1 (mPGES-1) and cytosolic PGE(2) synthase (cPGES) were reported to be expressed along the urogenital tracts. Here we report the genomic structure and tissue distribution of mPGES-2 in the urogenital system. Analysis of several bioinformatic databases demonstrated that mouse mPGES-2 spans 7 kb and consists of 7 exons. The mPGES-2 promoter contains multiple Sp1 sites and a GC box without a TATA box motif. Real-time quantitative PCR revealed that constitutive mPGES-2 mRNA was most abundant in the heart, brain, kidney and small intestine. In the urogenital system, mPGES-2 was highly expressed in the renal cortex, followed by the renal medulla and ovary, with lower levels in the ureter, bladder and uterus. Immunohistochemistry studies indicated that mPGES-2 was ubiquitously expressed along the nephron, with much lower levels in the glomeruli. In the ureter and bladder, mPGES-2 was mainly localized to the urothelium. In the reproductive system, mPGES-2 was restricted to the epithelial cells of the testis, epididymis, vas deferens and seminal vesicle in males, and oocytes, stroma cells and corpus luteum of the ovary and epithelial cells of the oviduct and uterus in females. This expression pattern is consistent with an important role for mPGES-2-mediated PGE(2) in urogenital function.

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Year:  2006        PMID: 17064959     DOI: 10.1016/j.bbalip.2006.06.018

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Enhanced pressor response to acute Ang II infusion in mice lacking membrane-associated prostaglandin E2 synthase-1.

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Journal:  Acta Pharmacol Sin       Date:  2010-09-27       Impact factor: 6.150

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Journal:  Am J Physiol Renal Physiol       Date:  2012-01-11

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6.  mPGES-2 deletion remarkably enhances liver injury in streptozotocin-treated mice via induction of GLUT2.

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Review 7.  Role of COX-2/mPGES-1/prostaglandin E2 cascade in kidney injury.

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Review 8.  An Update of Microsomal Prostaglandin E Synthase-1 and PGE2 Receptors in Cardiovascular Health and Diseases.

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Review 9.  Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney.

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Journal:  Kidney Res Clin Pract       Date:  2015-11-12

10.  Aggravation of acute kidney injury by mPGES-2 down regulation is associated with autophagy inhibition and enhanced apoptosis.

Authors:  Ting Li; Ying Liu; Jie Zhao; Shuying Miao; Yunfei Xu; Ke Liu; Meidong Liu; Guiliang Wang; Xianzhong Xiao
Journal:  Sci Rep       Date:  2017-08-31       Impact factor: 4.379

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