MiR-222-3p Regulates the Proliferation and Differentiation of C2C12 Myoblasts by Targeting BTG2

2019 ◽  
Vol 53 (1) ◽  
pp. 38-44
Author(s):  
D. L. Yang ◽  
M. L. Gan ◽  
Y. Tan ◽  
G. H. Ge ◽  
Q. Li ◽  
...  
2018 ◽  
Vol 54 (4) ◽  
pp. 304-310 ◽  
Author(s):  
Mailin Gan ◽  
Jingjing Du ◽  
Linyuan Shen ◽  
Dongli Yang ◽  
Anan Jiang ◽  
...  

Genes ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 64 ◽  
Author(s):  
Jing Zhang ◽  
Xin Xu ◽  
Yan Liu ◽  
Lin Zhang ◽  
Jack Odle ◽  
...  

This study was conducted to elucidate the biological effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on cell proliferation, differentiation and gene expression in C2C12 myoblasts. C2C12 were treated with various concentrations of EPA or DHA under proliferation and differentiation conditions. Cell viability was analyzed using cell counting kit-8 assays (CCK-8). The Edu assays were performed to analyze cell proliferation. To analyze cell differentiation, the expressions of myogenic marker genes were determined at the transcriptional and translational levels by qRT-PCR, immunoblotting and immunofluorescence. Global gene expression patterns were characterized using RNA-sequencing. Phosphorylation levels of ERK and Akt were examined by immunoblotting. Cell viability and proliferation was significantly inhibited after incubation with EPA (50 and 100 μM) or DHA (100 μM). Both EPA and DHA suppressed C2C12 myoblasts differentiation. RNA-sequencing analysis revealed that some muscle-related genes were significantly downregulated following EPA or DHA (50 μM) treatment, including insulin-like growth factor 2 (IGF-2), troponin T3 (Tnnt3), myoglobin (Mb), myosin light chain phosphorylatable fast skeletal muscle (Mylpf) and myosin heavy polypeptide 3 (Myh3). IGF-2 was crucial for the growth and differentiation of skeletal muscle and could activate the PI3K/Akt and the MAPK/ERK cascade. We found that EPA and DHA (50 μM) decreased the phosphorylation levels of ERK1/2 and Akt in C2C12 myoblasts. Thus, this study suggested that EPA and DHA exerted an inhibitory effect on myoblast proliferation and differentiation and downregulated muscle-related genes expression.


2017 ◽  
Vol 23 (3) ◽  
pp. 399-410 ◽  
Author(s):  
Daniel J. Bolus ◽  
Gobinath Shanmugam ◽  
Madhusudhanan Narasimhan ◽  
Namakkal S. Rajasekaran

2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Shaoting Fu ◽  
Xiaojing Lin ◽  
Lijun Yin ◽  
Xiaohui Wang

Abstract Background Androgen receptor (AR) exerts important roles in exercise-induced alterations of muscle mass, in which the proliferation and differentiation of satellite cells or myoblasts are crucial. Our previous study in C2C12 myoblasts demonstrated that 15% (mimic appropriate exercise) and 20% (mimic excessive exercise) stretches promoted and inhibited the proliferation respectively; and AR played a crucial role in 15% stretch-induced pro-proliferation through IGF-1-modulated PI3K/Akt, p38 and ERK1/2 pathways, but AR’s role in stretches-modulated proliferation of general myoblasts, especially 20% stretch, remains unclear, and the mechanisms need to be further clarified. Methods Firstly, the discrepancy in proliferation and the above indicators between L6 (without AR) and C2C12 (with AR) myoblasts were compared under 15% or 20% stretch. Then the influences of transfection AR or exogenous IGF-1 treatment on proliferation and these indicators were detected in stretched L6 myoblasts. Results (1) Under un-stretched state, the proliferation of L6 was slower than C2C12 cells. Furthermore, AR knockdown in C2C12 myoblasts repressed, while AR overexpression in L6 myoblasts promoted the proliferation. (2) 15% stretch-induced increases in the proliferation and activities of p38 and ERK1/2 were lower in L6 than C2C12 cells; AR overexpression enhanced the proliferation of 15% stretched L6 cells accompanied with the increases of p38 and ERK1/2 activities. (3) 20% stretch-induced anti-proliferation and inhibition of p38 activity were severer in L6 than C2C12 myoblasts; AR overexpression reversed the anti-proliferation of 20% stretch and enhanced p38 activity in L6 myoblasts. (4) In stretched L6 myoblasts, AR overexpression increased IGF-1R level despite no detectable IGF-1; and recombinant IGF-1 increased the proliferation, the level of IGF-1R, and the activities of p38 and ERK1/2 in 15% stretched L6 myoblasts. Conclusions The study demonstrated AR's crucial roles in stretches-regulated proliferation of myoblasts, and increased AR fulfilled 15% stretch's pro-proliferation via activating IGF-1R- p38 and ERK1/2 pathways while decreased AR achieved 20% stretch's anti-proliferation via inhibiting IGF-1R- p38 pathway, which is useful to understand in depth the role and mechanisms of AR in appropriate exercise increasing while excessive exercise decreasing muscle mass.


2013 ◽  
Vol 11 (3) ◽  
pp. 275
Author(s):  
Paola Pelegrineli Artilheiro ◽  
Jean Lucas Parpinelli Barbosa ◽  
Nadhia Helena Costa Souza ◽  
Mikaele Tavares da Silva ◽  
Sandra Kalil Bussadori ◽  
...  

<p class="MsoNormal" style="text-align: justify; mso-layout-grid-align: none; text-autospace: none;"><strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri;">Introdução</span></strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri;">: a miogênese é um processo essencial para a regeneração do tecido muscular após lesão. <strong>Objetivo</strong>: analisar a morfologia e a proliferação de mioblastos C2C12 durante o processo de diferenciação. <strong>Metodologia</strong>: os mioblastos foram cultivados em meio de manutenção (MM) (DMEM com 10% de SFB) e induzidos à diferenciação pela substituição por meio de diferenciação (MD) (DMEM com 2% soro de cavalo). A morfologia e proliferação celular foram avaliadas após 24, 48 e 96h de indução de diferenciação. A proliferação celular foi avaliada pelo método de MTT e as células foram fotografadas para análise da morfologia. <strong>Resultados</strong>: as células em MM apresentaram aumento significativo na proliferação quando comparadas às células em MD após 48 e 96h sendo observada uma maior confluência nestes mesmos períodos sem alteração da morfologia celular. <strong>Conclusão</strong>: os resultados podem facilitar no estabelecimento do período de análise para analisar a influência de algum tratamento sobre a proliferação e diferenciação de células musculares precursoras.</span></p><p class="MsoNormal"><strong>Palavras-chave</strong>: Morfologia. Proliferação. Diferenciação. Mioblastos.</p><p class="MsoNormal" style="text-align: justify; mso-layout-grid-align: none; text-autospace: none;"><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri;"><br /></span></p><p class="MsoNormal" style="text-align: justify; mso-layout-grid-align: none; text-autospace: none;"><span style="font-size: 10.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri; mso-ansi-language: EN-US;" lang="EN-US">Analysis of proliferation and morphology of C2C12 during cell differentiation</span></p><p class="MsoNormal" style="text-align: justify; mso-layout-grid-align: none; text-autospace: none;"><strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri; mso-ansi-language: EN-US;" lang="EN-US">Background</span></strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri; mso-ansi-language: EN-US;" lang="EN-US">: The myogenesis is a process essential for the repair of injured muscle fibers. <strong>Objective</strong>: to analyze the morphology and proliferation of C2C12 myoblasts during the differentiation process induced by horse serum. <strong>Methodology</strong>: The myoblasts were cultured in a culture of “Eagle” modified by Dulbecco, containing 10% fetal bovine serum (FBS), were induced to differentiate by replacing by DMEM containing 2% horse serum. Cells grown in DMEM containing 10% FBS analyzed in the same period served as controls. The morphology was assayed at 24, 48 and 96h after the addition of 2% horse serum or only during maintenance in DMEM 10% FCS. <strong>Results</strong>: The cells were photographed and the proliferation was assessed by MTT. <strong>Conclusion</strong>: our data can facilitate the establishment the best period to be used in order to analyze the influence of any treatment on the proliferation and differentiation of muscle cells.</span></p><p class="MsoNormal" style="text-align: justify;"><strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri; mso-ansi-language: EN-US;" lang="EN-US">Keywords:</span></strong><span style="font-size: 8.0pt; mso-ascii-font-family: Calibri; mso-hansi-font-family: Calibri; mso-bidi-font-family: Calibri; mso-ansi-language: EN-US;" lang="EN-US"> Morphology. Proliferation. Differentiation. Myoblasts.</span></p>


2017 ◽  
Vol 233 (2) ◽  
pp. 736-747 ◽  
Author(s):  
Seong Y. Hwang ◽  
Yong J. Kang ◽  
Bokyung Sung ◽  
Jung Y. Jang ◽  
Na L. Hwang ◽  
...  

Author(s):  
Xue Zhao ◽  
Hao Gu ◽  
Linghui Wang ◽  
Peiwen Zhang ◽  
Jingjing Du ◽  
...  

2018 ◽  
Vol 83 (2) ◽  
pp. 291-299 ◽  
Author(s):  
Guihua Ge ◽  
Dongli Yang ◽  
Ya Tan ◽  
Ying Chen ◽  
Dongmei Jiang ◽  
...  

2011 ◽  
Vol 29 (5) ◽  
pp. 378-383 ◽  
Author(s):  
Yang Feng ◽  
Jian-Hua Cao ◽  
Xin-Yun Li ◽  
Shu-Hong Zhao

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