دورية أكاديمية

Novel regulation of PKC-induced inflammation by Akt and protein phosphatase 2A in ovarian granulosa cells

التفاصيل البيبلوغرافية
العنوان: Novel regulation of PKC-induced inflammation by Akt and protein phosphatase 2A in ovarian granulosa cells
المؤلفون: Yen-Yu Lin, David Sun, Yuh-Lin Wu
المصدر: Chinese Journal of Physiology, Vol 63, Iss 4, Pp 179-186 (2020)
بيانات النشر: Wolters Kluwer Medknow Publications, 2020.
سنة النشر: 2020
المجموعة: LCC:Physiology
مصطلحات موضوعية: akt, granulosa cell, phorbol 12-myristate 13-acetate, protein phosphatase 2a, Physiology, QP1-981
الوصف: PKC-mediated inflammation is important in ovarian physiology. The roles of Akt and protein phosphatase 2A (PP2A) in PKC-mediated inflammation in ovarian granulosa cells (GCs) remain mostly unclear. PKC activator phorbol 12-myristate 13-acetate induced the Akt phosphorylation in rat primary GCs but reduced the Akt phosphorylation in KGN human GCs. In rat GCs, an inhibitory effect of PI3K inhibitor wortmannin and a stimulatory effect of Akt activator SC79 on PKC-induced cyclooxygenase-2 (COX-2)/PGE2production were noted; wortmannin and SC79 acted oppositely in human GCs. In rat GCs, PP2A inhibitor okadaic acid further enhanced the PKC-mediated promoter activation and elevation of mRNA and protein levels of the COX-2 gene, whereas PP2A activator sodium selenate attenuated the PKC-mediated COX-2 expression and promoter activation. PKC activation did not affect PP2A phosphorylation, but okadaic acid indeed augmented the PKC-induced NF-κB nuclear translocation. Thus, PP2A appears to act as a negative modulator in PKC-mediated cellular inflammation in rat GCs, at least in part due to its attenuating effect on the PKC-induced NF-κB activation.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0304-4920
2666-0059
العلاقة: http://www.cjphysiology.org/article.asp?issn=0304-4920;year=2020;volume=63;issue=4;spage=179;epage=186;aulast=LinTest; https://doaj.org/toc/0304-4920Test; https://doaj.org/toc/2666-0059Test
DOI: 10.4103/CJP.CJP_44_20
الوصول الحر: https://doaj.org/article/936ee98216614ca7a3baa60e32f190aaTest
رقم الانضمام: edsdoj.936ee98216614ca7a3baa60e32f190aa
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:03044920
26660059
DOI:10.4103/CJP.CJP_44_20