Title : mPGES-1-Derived PGE2 Contributes to Indoxyl Sulfate-Induced Mesangial Cell Proliferation.

Pub. Date : 2017

PMID : 28854439






7 Functional Relationships(s)
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1 mPGES-1-Derived PGE2 Contributes to Indoxyl Sulfate-Induced Mesangial Cell Proliferation. Dinoprostone prostaglandin E synthase Mus musculus
2 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. Dinoprostone prostaglandin E synthase Mus musculus
3 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. Dinoprostone prostaglandin E synthase Mus musculus
4 Interestingly, silencing mPGES-1 reduced cell number in S and G2 phases and blocked the upregulation of cyclin A2 and cyclin D1 in parallel with blunted PGE2 release after IS treatment, indicating that mPGES-1-derived PGE2 could contribute to MC proliferation. Dinoprostone prostaglandin E synthase Mus musculus
5 Interestingly, silencing mPGES-1 reduced cell number in S and G2 phases and blocked the upregulation of cyclin A2 and cyclin D1 in parallel with blunted PGE2 release after IS treatment, indicating that mPGES-1-derived PGE2 could contribute to MC proliferation. Dinoprostone prostaglandin E synthase Mus musculus
6 Interestingly, silencing mPGES-1 reduced cell number in S and G2 phases and blocked the upregulation of cyclin A2 and cyclin D1 in parallel with blunted PGE2 release after IS treatment, indicating that mPGES-1-derived PGE2 could contribute to MC proliferation. Dinoprostone prostaglandin E synthase Mus musculus
7 CONCLUSION: mPGES-1-derived PGE2 contributed to IS-induced mesangial cell proliferation. Dinoprostone prostaglandin E synthase Mus musculus