Adipose-derived stem cells enhance myogenic differentiation in the mdx mouse model of muscular dystrophy via paracrine signaling
Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipose-derived stem cells (6 × 10 6 ) were injected int...
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Published in | Neural regeneration research Vol. 11; no. 10; pp. 1638 - 1643 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Wolters Kluwer India Pvt. Ltd
01.10.2016
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Abstract | Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipose-derived stem cells (6 × 10 6 ) were injected into the gastrocnemius muscle of mdx mice at various sites. Dystrophin expression was found in the muscle fibers. Phosphorylation levels of Akt, mammalian target of rapamycin (mTOR), eIF-4E binding protein 1 and S6 kinase 1 were increased, and the Akt/mTOR pathway was activated. Simultaneously, myogenin levels were increased, whereas cleaved caspase 3 and vimentin levels were decreased. Necrosis and fibrosis were reduced in the muscle fibers. These findings suggest that adipose-derived stem cells promote the regeneration and survival of muscle cells by inhibiting apoptosis and fibrosis, thereby alleviating muscle damage in muscular dystrophy. |
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AbstractList | Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipose-derived stem cells (6 × 10 6 ) were injected into the gastrocnemius muscle of mdx mice at various sites. Dystrophin expression was found in the muscle fibers. Phosphorylation levels of Akt, mammalian target of rapamycin (mTOR), eIF-4E binding protein 1 and S6 kinase 1 were increased, and the Akt/mTOR pathway was activated. Simultaneously, myogenin levels were increased, whereas cleaved caspase 3 and vimentin levels were decreased. Necrosis and fibrosis were reduced in the muscle fibers. These findings suggest that adipose-derived stem cells promote the regeneration and survival of muscle cells by inhibiting apoptosis and fibrosis, thereby alleviating muscle damage in muscular dystrophy. Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipose-derived stem cells (6 × 10 6 ) were injected into the gastrocnemius muscle of mdx mice at various sites. Dystrophin expression was found in the muscle fibers. Phosphorylation levels of Akt, mammalian target of rapamycin (mTOR), eIF-4E binding protein 1 and S6 kinase 1 were increased, and the Akt/mTOR pathway was activated. Simultaneously, myogenin levels were increased, whereas cleaved caspase 3 and vimentin levels were decreased. Necrosis and fibrosis were reduced in the muscle fibers. These findings suggest that adipose-derived stem cells promote the regeneration and survival of muscle cells by inhibiting apoptosis and fibrosis, thereby alleviating muscle damage in muscular dystrophy. Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipose-derived stem cells (6 × 10 ) were injected into the gastrocnemius muscle of mdx mice at various sites. Dystrophin expression was found in the muscle fibers. Phosphorylation levels of Akt, mammalian target of rapamycin (mTOR), eIF-4E binding protein 1 and S6 kinase 1 were increased, and the Akt/mTOR pathway was activated. Simultaneously, myogenin levels were increased, whereas cleaved caspase 3 and vimentin levels were decreased. Necrosis and fibrosis were reduced in the muscle fibers. These findings suggest that adipose-derived stem cells promote the regeneration and survival of muscle cells by inhibiting apoptosis and fibrosis, thereby alleviating muscle damage in muscular dystrophy. |
Audience | Academic |
Author | Yang, Li-qing Li, Ya-qin Cao, Ji-qing Zhang, Cheng Zhu, Yu-ling Yang, Juan Geng, Jia Zhang, Hui-li Feng, Shan-wei Kong, Jie Liang, Ying-yin |
AuthorAffiliation | 2 Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province, China 1 Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province, China 4 Department of Neurology, Yantai Yuhuangding Hospital, Yantai, Shandong Province, China 3 First Affiliated Hospital, Kunming Medical College, Kunming, Yunnan Province, China |
AuthorAffiliation_xml | – name: 1 Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province, China – name: 2 Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province, China – name: 4 Department of Neurology, Yantai Yuhuangding Hospital, Yantai, Shandong Province, China – name: 3 First Affiliated Hospital, Kunming Medical College, Kunming, Yunnan Province, China |
Author_xml | – sequence: 1 givenname: Ji-qing surname: Cao fullname: Cao, Ji-qing organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 2 givenname: Ying-yin surname: Liang fullname: Liang, Ying-yin organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 3 givenname: Ya-qin surname: Li fullname: Li, Ya-qin organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 4 givenname: Hui-li surname: Zhang fullname: Zhang, Hui-li organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 5 givenname: Yu-ling surname: Zhu fullname: Zhu, Yu-ling organization: First Affiliated Hospital, Kunming Medical College, Kunming, Yunnan Province – sequence: 6 givenname: Jia surname: Geng fullname: Geng, Jia organization: Department of Neurology, Yantai Yuhuangding Hospital, Yantai, Shandong Province – sequence: 7 givenname: Li-qing surname: Yang fullname: Yang, Li-qing organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 8 givenname: Shan-wei surname: Feng fullname: Feng, Shan-wei organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 9 givenname: Juan surname: Yang fullname: Yang, Juan organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 10 givenname: Jie surname: Kong fullname: Kong, Jie organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province; Guangdong Key Laboratory for the Diagnosis and Treatment of Major Neurological Disease, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province – sequence: 11 givenname: Cheng surname: Zhang fullname: Zhang, Cheng organization: Department of Neurology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27904496$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1089_hum_2017_213 crossref_primary_10_18632_aging_102802 crossref_primary_10_1002_mus_26614 crossref_primary_10_3390_cells10071803 crossref_primary_10_1016_j_mtadv_2024_100465 |
Cites_doi | 10.1038/mt.2011.181 10.1002/jcb.24619 10.1155/2014/129048 10.1038/sj.emboj.7600917 10.3727/096368914X678599 10.1016/j.transproceed.2010.04.031 10.1038/ncb1101-1014 10.3109/14653249.2012.688944 10.1074/jbc.M304583200 10.1093/hmg/ddv316 10.2119/molmed.2010.00256 10.1002/jgm.603 10.1083/jcb.200903131 10.1091/mbc.E02-02-0105 10.1016/j.bbrc.2007.09.058 10.1038/mt.2009.67 10.1042/BC20070102 10.1089/scd.2006.0118 10.1038/sj.cdd.4400738 10.1089/scd.2011.0403 |
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Keywords | adipose-derived stem cells myogenic differentiation; paracrine pathway nerve regeneration neural regeneration dystrophin Duchenne muscular dystrophy |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: JQC collected the data, designed and performed the experiment and wrote the paper. YYL, YQL, HLZ and YLZ collected and analyzed the data. JG, LQY, SWF, JY and JK performed the experiment and analyzed the data. CZ designed the study, revised the paper. All authors approved the final version of the paper. These authors contributed equally to this paper. |
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Snippet | Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is... |
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SubjectTerms | Analysis Care and treatment Health aspects Immunoglobulins Insulin Insulin-like growth factors Laboratory animals Morphology Muscular dystrophy Mutation Myogenesis nerve regeneration; Duchenne muscular dystrophy; adipose-derived stem cells; myogenic differentiation; paracrine pathway; dystrophin; neural regeneration Protein binding Proteins Radiation therapy Rodents Statistical analysis Stem cell transplantation Stem cells |
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Title | Adipose-derived stem cells enhance myogenic differentiation in the mdx mouse model of muscular dystrophy via paracrine signaling |
URI | http://www.nrronline.org/article.asp?issn=1673-5374;year=2016;volume=11;issue=10;spage=1638;epage=1643;aulast=Cao;type=0 https://www.ncbi.nlm.nih.gov/pubmed/27904496 https://www.proquest.com/docview/2382723875/abstract/ https://search.proquest.com/docview/1845250615 https://pubmed.ncbi.nlm.nih.gov/PMC5116844 https://doaj.org/article/389b50d152e84bfa895a42550bca8a41 |
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