دورية أكاديمية

Regulation of CXCL1 chemokine and CSF3 cytokine levels in myometrial cells by the MAFF transcription factor.

التفاصيل البيبلوغرافية
العنوان: Regulation of CXCL1 chemokine and CSF3 cytokine levels in myometrial cells by the MAFF transcription factor.
المؤلفون: Saliba J; Lady Davis Institute for Medical Research, Montreal, Quebec, Canada., Coutaud B; Lady Davis Institute for Medical Research, Montreal, Quebec, Canada., Solovieva V; Lady Davis Institute for Medical Research, Montreal, Quebec, Canada., Lu F; Lady Davis Institute for Medical Research, Montreal, Quebec, Canada., Blank V; Lady Davis Institute for Medical Research, Montreal, Quebec, Canada.; Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.; Department of Physiology, McGill University, Montreal, Quebec, Canada.
المصدر: Journal of cellular and molecular medicine [J Cell Mol Med] 2019 Apr; Vol. 23 (4), pp. 2517-2525. Date of Electronic Publication: 2019 Jan 22.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101083777 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1582-4934 (Electronic) Linking ISSN: 15821838 NLM ISO Abbreviation: J Cell Mol Med Subsets: MEDLINE
أسماء مطبوعة: Publication: Oxford, England : Wiley-Blackwell
Original Publication: Bucharest : "Carol Davila" University Press, 2000-
مواضيع طبية MeSH: Chemokine CXCL1/*genetics , Granulocyte Colony-Stimulating Factor/*genetics , MafF Transcription Factor/*genetics , Matrix Metalloproteinases/*genetics , Myocytes, Smooth Muscle/*metabolism , Myometrium/*metabolism , Nuclear Proteins/*genetics, Cell Line ; Chemokine CXCL1/metabolism ; Female ; Gene Expression Regulation ; Granulocyte Colony-Stimulating Factor/metabolism ; Humans ; MafF Transcription Factor/antagonists & inhibitors ; MafF Transcription Factor/metabolism ; Matrix Metalloproteinases/metabolism ; Myocytes, Smooth Muscle/cytology ; Myometrium/cytology ; Nuclear Proteins/antagonists & inhibitors ; Nuclear Proteins/metabolism ; Paracrine Communication ; Pregnancy ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; RNA, Small Interfering/genetics ; RNA, Small Interfering/metabolism ; Signal Transduction ; THP-1 Cells ; Transcription, Genetic
مستخلص: Cytokines play key roles in a variety of reproductive processes including normal parturition as well as preterm birth. Our previous data have shown that MAFF, a member of the MAF family of bZIP transcription factors, is rapidly induced by pro-inflammatory cytokines in PHM1-31 myometrial cells. We performed loss-of-function studies in PHM1-31 cells to identify MAFF dependent genes. We showed that knockdown of MAFF significantly decreased CXCL1 chemokine and CSF3 cytokine transcript and protein levels. Using chromatin immunoprecipitation analyzes, we confirmed CXCL1 and CSF3 genes as direct MAFF targets. We also demonstrated that MAFF function in PHM1-31 myometrial cells is able to control cytokine and matrix metalloproteinase gene expression in THP-1 monocytic cells in a paracrine fashion. Our studies provide valuable insights into the MAFF dependent transcriptional network governing myometrial cell function. The data suggest a role of MAFF in parturition and/or infection-induced preterm labour through modulation of inflammatory processes in the microenvironment.
(© 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.)
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فهرسة مساهمة: Keywords: MAFF; CSF3; CXCL1; IL1B; cytokines; myometrium
المشرفين على المادة: 0 (CXCL1 protein, human)
0 (Chemokine CXCL1)
0 (MAFF protein, human)
0 (MafF Transcription Factor)
0 (Nuclear Proteins)
0 (RNA, Messenger)
0 (RNA, Small Interfering)
143011-72-7 (Granulocyte Colony-Stimulating Factor)
EC 3.4.24.- (Matrix Metalloproteinases)
تواريخ الأحداث: Date Created: 20190123 Date Completed: 20200715 Latest Revision: 20210109
رمز التحديث: 20240513
مُعرف محوري في PubMed: PMC6433675
DOI: 10.1111/jcmm.14136
PMID: 30669188
قاعدة البيانات: MEDLINE
الوصف
تدمد:1582-4934
DOI:10.1111/jcmm.14136