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The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell

Scope: Four and a half LIM domain protein 2 (FHL2) is a LIM domain protein expressed in muscle tissue whose deletion is causative of myopathies. Although FHL2 has a confirmed important role in muscle development, its autophagy-related function in muscle differentiation has not been fully determined....

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Autores principales: Liu, Zihao, Han, Shunshun, Wang, Yan, Cui, Can, Zhu, Qing, Jiang, Xiaosong, Yang, Chaowu, Du, Huarui, Yu, Chunlin, Li, Qingyun, He, Haorong, Shen, Xiaoxu, Chen, Yuqi, Zhang, Yao, Ye, Lin, Zhang, Zhichao, Li, Diyan, Zhao, Xiaoling, Yin, Huadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429013/
https://www.ncbi.nlm.nih.gov/pubmed/30906214
http://dx.doi.org/10.7150/ijbs.31371
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author Liu, Zihao
Han, Shunshun
Wang, Yan
Cui, Can
Zhu, Qing
Jiang, Xiaosong
Yang, Chaowu
Du, Huarui
Yu, Chunlin
Li, Qingyun
He, Haorong
Shen, Xiaoxu
Chen, Yuqi
Zhang, Yao
Ye, Lin
Zhang, Zhichao
Li, Diyan
Zhao, Xiaoling
Yin, Huadong
author_facet Liu, Zihao
Han, Shunshun
Wang, Yan
Cui, Can
Zhu, Qing
Jiang, Xiaosong
Yang, Chaowu
Du, Huarui
Yu, Chunlin
Li, Qingyun
He, Haorong
Shen, Xiaoxu
Chen, Yuqi
Zhang, Yao
Ye, Lin
Zhang, Zhichao
Li, Diyan
Zhao, Xiaoling
Yin, Huadong
author_sort Liu, Zihao
collection PubMed
description Scope: Four and a half LIM domain protein 2 (FHL2) is a LIM domain protein expressed in muscle tissue whose deletion is causative of myopathies. Although FHL2 has a confirmed important role in muscle development, its autophagy-related function in muscle differentiation has not been fully determined. Methods: C2C12 cells were treated with FHL2-konwdown or FHL2-overexpression. The morphology of C2C12 cells was observed by transmission electron microscopy. The mRNA and protein abundances of muscle related genes and autophagy related genes were measured by RT-PCR and western blot. Immunofluorescence and co-immunoprecipitation assay were used to verify the interaction between FHL2 and LC3 protein. Results: FHL2 silencing reduced LC3-Ⅱ protein expression and the amount of LC3 that co-immunoprecipitated with FHL2, indicating that FHL2 interacts with LC3-Ⅱ in the formation of autophagosomes. Moreover, the expression of muscle development marker genes such as MyoD1 and MyoG was lower in FHL2-silenced C2C12 cells but not in FHL2-overexpressing C2C12 cells. Electron microscopy analysis revealed large empty autophagosomes in FHL2-silenced myoblasts, while flow cytometry suggested that FHL2 silencing made cells more vulnerable to staurosporine-induced cell death. Conclusion: These results suggest that FHL2 interacts with LC3-Ⅱ in autophagosome formation to regulate the development of muscle cells.
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spelling pubmed-64290132019-03-22 The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell Liu, Zihao Han, Shunshun Wang, Yan Cui, Can Zhu, Qing Jiang, Xiaosong Yang, Chaowu Du, Huarui Yu, Chunlin Li, Qingyun He, Haorong Shen, Xiaoxu Chen, Yuqi Zhang, Yao Ye, Lin Zhang, Zhichao Li, Diyan Zhao, Xiaoling Yin, Huadong Int J Biol Sci Research Paper Scope: Four and a half LIM domain protein 2 (FHL2) is a LIM domain protein expressed in muscle tissue whose deletion is causative of myopathies. Although FHL2 has a confirmed important role in muscle development, its autophagy-related function in muscle differentiation has not been fully determined. Methods: C2C12 cells were treated with FHL2-konwdown or FHL2-overexpression. The morphology of C2C12 cells was observed by transmission electron microscopy. The mRNA and protein abundances of muscle related genes and autophagy related genes were measured by RT-PCR and western blot. Immunofluorescence and co-immunoprecipitation assay were used to verify the interaction between FHL2 and LC3 protein. Results: FHL2 silencing reduced LC3-Ⅱ protein expression and the amount of LC3 that co-immunoprecipitated with FHL2, indicating that FHL2 interacts with LC3-Ⅱ in the formation of autophagosomes. Moreover, the expression of muscle development marker genes such as MyoD1 and MyoG was lower in FHL2-silenced C2C12 cells but not in FHL2-overexpressing C2C12 cells. Electron microscopy analysis revealed large empty autophagosomes in FHL2-silenced myoblasts, while flow cytometry suggested that FHL2 silencing made cells more vulnerable to staurosporine-induced cell death. Conclusion: These results suggest that FHL2 interacts with LC3-Ⅱ in autophagosome formation to regulate the development of muscle cells. Ivyspring International Publisher 2019-03-01 /pmc/articles/PMC6429013/ /pubmed/30906214 http://dx.doi.org/10.7150/ijbs.31371 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Liu, Zihao
Han, Shunshun
Wang, Yan
Cui, Can
Zhu, Qing
Jiang, Xiaosong
Yang, Chaowu
Du, Huarui
Yu, Chunlin
Li, Qingyun
He, Haorong
Shen, Xiaoxu
Chen, Yuqi
Zhang, Yao
Ye, Lin
Zhang, Zhichao
Li, Diyan
Zhao, Xiaoling
Yin, Huadong
The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title_full The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title_fullStr The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title_full_unstemmed The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title_short The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell
title_sort lim-only protein fhl2 is involved in autophagy to regulate the development of skeletal muscle cell
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429013/
https://www.ncbi.nlm.nih.gov/pubmed/30906214
http://dx.doi.org/10.7150/ijbs.31371
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