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Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension

BACKGROUND: Since the use of human umbilical cord Wharton’s Jelly derived mesenchymal stromal cells (hWJ-MSCs) to treat sarcopenia has not been explored, we studied the effects of hWJ-MSCs in aged male C57BL/6J mice with sarcopenia induced by hindlimb suspension, and explored the potential mechanism...

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Autores principales: Wang, Quan-Quan, Jing, Xiao-Ma, Bi, Yan-Zhen, Cao, Xiao-Fu, Wang, Yu-Zhong, Li, Yan-Xin, Qiao, Bao-Jun, Chen, Yun, Hao, Yan-Lei, Hu, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320659/
https://www.ncbi.nlm.nih.gov/pubmed/30571669
http://dx.doi.org/10.12659/MSM.913362
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author Wang, Quan-Quan
Jing, Xiao-Ma
Bi, Yan-Zhen
Cao, Xiao-Fu
Wang, Yu-Zhong
Li, Yan-Xin
Qiao, Bao-Jun
Chen, Yun
Hao, Yan-Lei
Hu, Jing
author_facet Wang, Quan-Quan
Jing, Xiao-Ma
Bi, Yan-Zhen
Cao, Xiao-Fu
Wang, Yu-Zhong
Li, Yan-Xin
Qiao, Bao-Jun
Chen, Yun
Hao, Yan-Lei
Hu, Jing
author_sort Wang, Quan-Quan
collection PubMed
description BACKGROUND: Since the use of human umbilical cord Wharton’s Jelly derived mesenchymal stromal cells (hWJ-MSCs) to treat sarcopenia has not been explored, we studied the effects of hWJ-MSCs in aged male C57BL/6J mice with sarcopenia induced by hindlimb suspension, and explored the potential mechanism. MATERIAL/METHODS: Hindlimb suspension was used to induce sarcopenia in 24-month-old C57BL/6J mice and green fluorescent protein-tagged hWJ-MSCs and controls were transplanted into mice via tail vein or local intramuscular injection. After hWJ-MSC transplantation, changes in whole body muscle strength and endurance, gastrocnemius muscle weight and myofiber cross-sectional area (CSA) were studied. Proliferation of skeletal muscle stem cell, apoptosis, and chronic inflammation were also investigated. RESULTS: We demonstrated that whole body muscle strength and endurance, gastrocnemius muscle mass, and CSA were significantly increased in hWJ-MSC-transplanted mice than in controls (P<0.05). In hWJ-MSC-transplanted mice, apoptotic myonuclei was reduced, and BrdU and Pax-7 expression indices of gastrocnemius muscles were increased (P<0.05). Tumor necrosis factor (TNF)-α and interleukin (IL)-6 were downregulated, and IL-4 and IL-10 were upregulated (P<0.05). CONCLUSIONS: hWJ-MSCs may ameliorate sarcopenia in aged male C57BL/6J mice induced by hindlimb suspension, and this may be via activation of resident skeletal muscle satellite cells, reduction of apoptosis, and less chronic inflammation.
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spelling pubmed-63206592019-01-25 Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension Wang, Quan-Quan Jing, Xiao-Ma Bi, Yan-Zhen Cao, Xiao-Fu Wang, Yu-Zhong Li, Yan-Xin Qiao, Bao-Jun Chen, Yun Hao, Yan-Lei Hu, Jing Med Sci Monit Animal Study BACKGROUND: Since the use of human umbilical cord Wharton’s Jelly derived mesenchymal stromal cells (hWJ-MSCs) to treat sarcopenia has not been explored, we studied the effects of hWJ-MSCs in aged male C57BL/6J mice with sarcopenia induced by hindlimb suspension, and explored the potential mechanism. MATERIAL/METHODS: Hindlimb suspension was used to induce sarcopenia in 24-month-old C57BL/6J mice and green fluorescent protein-tagged hWJ-MSCs and controls were transplanted into mice via tail vein or local intramuscular injection. After hWJ-MSC transplantation, changes in whole body muscle strength and endurance, gastrocnemius muscle weight and myofiber cross-sectional area (CSA) were studied. Proliferation of skeletal muscle stem cell, apoptosis, and chronic inflammation were also investigated. RESULTS: We demonstrated that whole body muscle strength and endurance, gastrocnemius muscle mass, and CSA were significantly increased in hWJ-MSC-transplanted mice than in controls (P<0.05). In hWJ-MSC-transplanted mice, apoptotic myonuclei was reduced, and BrdU and Pax-7 expression indices of gastrocnemius muscles were increased (P<0.05). Tumor necrosis factor (TNF)-α and interleukin (IL)-6 were downregulated, and IL-4 and IL-10 were upregulated (P<0.05). CONCLUSIONS: hWJ-MSCs may ameliorate sarcopenia in aged male C57BL/6J mice induced by hindlimb suspension, and this may be via activation of resident skeletal muscle satellite cells, reduction of apoptosis, and less chronic inflammation. International Scientific Literature, Inc. 2018-12-20 /pmc/articles/PMC6320659/ /pubmed/30571669 http://dx.doi.org/10.12659/MSM.913362 Text en © Med Sci Monit, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Animal Study
Wang, Quan-Quan
Jing, Xiao-Ma
Bi, Yan-Zhen
Cao, Xiao-Fu
Wang, Yu-Zhong
Li, Yan-Xin
Qiao, Bao-Jun
Chen, Yun
Hao, Yan-Lei
Hu, Jing
Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title_full Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title_fullStr Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title_full_unstemmed Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title_short Human Umbilical Cord Wharton’s Jelly Derived Mesenchymal Stromal Cells May Attenuate Sarcopenia in Aged Mice Induced by Hindlimb Suspension
title_sort human umbilical cord wharton’s jelly derived mesenchymal stromal cells may attenuate sarcopenia in aged mice induced by hindlimb suspension
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320659/
https://www.ncbi.nlm.nih.gov/pubmed/30571669
http://dx.doi.org/10.12659/MSM.913362
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