دورية أكاديمية

TβRII Regulates the Proliferation of Metanephric Mesenchyme Cells through Six2 In Vitro

التفاصيل البيبلوغرافية
العنوان: TβRII Regulates the Proliferation of Metanephric Mesenchyme Cells through Six2 In Vitro
المؤلفون: Zhaomin Mao, Zhongshi Lyu, Liyuan Huang, Qin Zhou, Yaguang Weng
المصدر: International Journal of Molecular Sciences, Vol 18, Iss 4, p 853 (2017)
بيانات النشر: MDPI AG, 2017.
سنة النشر: 2017
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: TβRII, Six2, Smad3, kidney development, proliferation, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: The transforming growth factor-β (TGFβ) family signaling pathways play an important role in regulatory cellular networks and exert specific effects on developmental programs during embryo development. However, the function of TGFβ signaling pathways on the early kidney development remains unclear. In this work, we aim to detect the underlying role of TGFβ type II receptor (TβRII) in vitro, which has a similar expression pattern as the crucial regulator Six2 during early kidney development. Firstly, the 5-ethynyl-2′-deoxyuridine (EdU) assay showed knock down of TβRII significantly decreased the proliferation ratio of metanephric mesenchyme (MM) cells. Additionally, real-time Polymerase Chain Reaction (PCR) and Western blot together with immunofluorescence determined that the mRNA and protein levels of Six2 declined after TβRII knock down. Also, Six2 was observed to be able to partially rescue the proliferation phenotype caused by the depletion of TβRII. Moreover, bioinformatics analysis and luciferase assay indicated Smad3 could transcriptionally target Six2. Further, the EdU assay showed that Smad3 could also rescue the inhibition of proliferation caused by the knock down of TβRII. Taken together, these findings delineate the important function of the TGFβ signaling pathway in the early development of kidney and TβRII was shown to be able to promote the expression of Six2 through Smad3 mediating transcriptional regulation and in turn activate the proliferation of MM cells.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1422-0067
18040853
Relation: http://www.mdpi.com/1422-0067/18/4/853; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms18040853
URL الوصول: https://doaj.org/article/efa7be19dbe24de9a0f470b749ee791f
رقم الأكسشن: edsdoj.fa7be19dbe24de9a0f470b749ee791f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14220067
18040853
DOI:10.3390/ijms18040853