دورية أكاديمية

Impairment of Hepcidin Upregulation by Lipopolysaccharide in the Interleukin-6 Knockout Mouse Brain

التفاصيل البيبلوغرافية
العنوان: Impairment of Hepcidin Upregulation by Lipopolysaccharide in the Interleukin-6 Knockout Mouse Brain
المؤلفون: Fa-Li Zhang, Hui-Min Hou, Zhi-Nan Yin, Lan Chang, Fe-Mi Li, Y.-J. Chen, Ya Ke, Zhong-Ming Qian
المصدر: Frontiers in Molecular Neuroscience, Vol 10 (2017)
بيانات النشر: Frontiers Media S.A., 2017.
سنة النشر: 2017
المجموعة: LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
مصطلحات موضوعية: hepcidin, IL-6+/+ and IL-6-/- mice, signal transducer and activator of transcription 3 (STAT3), ferroportin 1 (Fpn1) and ferritin light chain (Ft-L), cortex and hippocampus, lipopolysaccharide (LPS), Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
الوصف: To find out whether the Interleukin-6 (IL-6)/signal transducer and activator of transcription 3 (STAT3) signaling pathway is involved in the expression of hepcidin in the mouse brain in vivo, we investigated the phosphorylation of STAT3, as well as the expression of hepcidin mRNA, ferroportin 1 (Fpn1) and ferritin light chain (Ft-L) proteins in the cortex and hippocampus of LPS-treated wild type (IL-6+/+) and IL-6 knockout (IL-6-/-) mice. We demonstrated that IL-6 knockout could significantly reduce the response of hepcidin mRNA, phospho-STAT3, Fpn1 and Ft-L protein expression to LPS treatment, in both the cortex and hippocampus of mice. Also, Stattic, an inhibitor of STAT3, significantly reduced the expression of phospho-STAT3 and hepcidin mRNA in the cortex and hippocampus of the LPS-treated wild type mice. These findings provide in vivo evidence for the involvement of the IL-6/STAT3 signaling pathway in the expression of hepcidin.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1662-5099
Relation: http://journal.frontiersin.org/article/10.3389/fnmol.2017.00367/full; https://doaj.org/toc/1662-5099
DOI: 10.3389/fnmol.2017.00367
URL الوصول: https://doaj.org/article/a59a2ddcfaa341b597a901ac55666ffa
رقم الأكسشن: edsdoj.59a2ddcfaa341b597a901ac55666ffa
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16625099
DOI:10.3389/fnmol.2017.00367