TNF-α and IGF1 modify the microRNA signature in skeletal muscle cell differentiation

被引:37
|
作者
Meyer, Swanhild U. [1 ]
Thirion, Christian [2 ]
Polesskaya, Anna [3 ]
Bauersachs, Stefan [4 ]
Kaiser, Sebastian [5 ]
Krause, Sabine [6 ]
Pfaffl, Michael W. [1 ]
机构
[1] Tech Univ Munich, ZIEL Res Ctr Nutr & Food Sci, Physiol Weihenstephan, D-85354 Freising Weihenstephan, Germany
[2] SIRION Biotech GmbH, D-82152 Martinsried, Germany
[3] Univ Paris 11, iBiTec S SBIGeM, CEA Saclay, CNRS FRE 3377, F-91191 Gif Sur Yvette, France
[4] Ludwig Maximilians Univ Munchen, Gene Ctr, Lab Funct Genome Anal LAFUGA, D-81377 Munich, Germany
[5] Univ Munich, Dept Stat, D-80539 Munich, Germany
[6] Univ Munich, Friedrich Baur Inst, Dept Neurol, D-81377 Munich, Germany
关键词
microRNA; TNF-alpha; IGF1; Skeletal muscle cell; Expression profiling; Myoblast differentiation; Human; Murine; miRNA biogenesis; MAPK; TUMOR-NECROSIS-FACTOR; MYOGENIC DIFFERENTIATION; GENE-EXPRESSION; HUMAN MYOBLASTS; GROWTH-FACTORS; MESSENGER-RNA; MIRNA; ACTIVATION; INSULIN; PROTEIN;
D O I
10.1186/s12964-015-0083-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Elevated levels of the inflammatory cytokine TNF-alpha are common in chronic diseases or inherited or degenerative muscle disorders and can lead to muscle wasting. By contrast, IGF1 has a growth promoting effect on skeletal muscle. The molecular mechanisms mediating the effect of TNF-alpha and IGF1 on muscle cell differentiation are not completely understood. Muscle cell proliferation and differentiation are regulated by microRNAs (miRNAs) which play a dominant role in this process. This study aims at elucidating how TNF-alpha or IGF1 regulate microRNA expression to affect myoblast differentiation and myotube formation. Results: In this study, we analyzed the impact of TNF-alpha or IGF1 treatment on miRNA expression in myogenic cells. Results reveal that i) TNF-alpha and IGF1 regulate miRNA expression during skeletal muscle cell differentiation in vitro, ii) microRNA targets can mediate the negative effect of TNF-alpha on fusion capacity of skeletal myoblasts by targeting genes associated with axon guidance, MAPK signalling, focal adhesion, and neurotrophin signalling pathway, iii) inhibition of miR-155 in combination with overexpression of miR-503 partially abrogates the inhibitory effect of TNF-alpha on myotube formation, and iv) MAPK/ERK inhibition might participate in modulating the effect of TNF-alpha and IGF1 on miRNA abundance. Conclusions: The inhibitory effects of TNF-alpha or the growth promoting effects of IGF1 on skeletal muscle differentiation include the deregulation of known muscle-regulatory miRNAs as well as miRNAs which have not yet been associated with skeletal muscle differentiation or response to TNF-alpha or IGF1. This study indicates that miRNAs are mediators of the inhibitory effect of TNF-alpha on myoblast differentiation. We show that intervention at the miRNA level can ameliorate the negative effect of TNF-alpha by promoting myoblast differentiation. Moreover, we cautiously suggest that TNF-alpha or IGF1 modulate the miRNA biogenesis of some miRNAs via MAPK/ERK signalling. Finally, this study identifies indicative biomarkers of myoblast differentiation and cytokine influence and points to novel RNA targets.
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页数:14
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