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Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration

Skeletal muscle regeneration requires the highly coordinated cooperation of muscle satellite cells (MuSCs) with other cellular components. Upon injury, myeloid cells populate the wound site, concomitant with MuSC activation. However, detailed analysis of MuSC–myeloid cell interaction is hindered by...

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Autores principales: He, Yingzhu, Heng, Youshan, Qin, Zhongya, Wei, Xiuqing, Wu, Zhenguo, Qu, Jianan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584350/
https://www.ncbi.nlm.nih.gov/pubmed/37851799
http://dx.doi.org/10.1126/sciadv.adi1891
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author He, Yingzhu
Heng, Youshan
Qin, Zhongya
Wei, Xiuqing
Wu, Zhenguo
Qu, Jianan
author_facet He, Yingzhu
Heng, Youshan
Qin, Zhongya
Wei, Xiuqing
Wu, Zhenguo
Qu, Jianan
author_sort He, Yingzhu
collection PubMed
description Skeletal muscle regeneration requires the highly coordinated cooperation of muscle satellite cells (MuSCs) with other cellular components. Upon injury, myeloid cells populate the wound site, concomitant with MuSC activation. However, detailed analysis of MuSC–myeloid cell interaction is hindered by the lack of suitable live animal imaging technology. Here, we developed a dual-laser multimodal nonlinear optical microscope platform to study the dynamics of MuSCs and their interaction with nonmyogenic cells during muscle regeneration. Using three-dimensional time-lapse imaging on live reporter mice and taking advantages of the autofluorescence of reduced nicotinamide adenine dinucleotide (NADH), we studied the spatiotemporal interaction between nonmyogenic cells and muscle stem/progenitor cells during MuSC activation and proliferation. We discovered that their cell-cell contact was transient in nature. Moreover, MuSCs could activate with notably reduced infiltration of neutrophils and macrophages, and their proliferation, although dependent on macrophages, did not require constant contact with them. These findings provide a fresh perspective on myeloid cells’ role during muscle regeneration.
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spelling pubmed-105843502023-10-19 Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration He, Yingzhu Heng, Youshan Qin, Zhongya Wei, Xiuqing Wu, Zhenguo Qu, Jianan Sci Adv Biomedicine and Life Sciences Skeletal muscle regeneration requires the highly coordinated cooperation of muscle satellite cells (MuSCs) with other cellular components. Upon injury, myeloid cells populate the wound site, concomitant with MuSC activation. However, detailed analysis of MuSC–myeloid cell interaction is hindered by the lack of suitable live animal imaging technology. Here, we developed a dual-laser multimodal nonlinear optical microscope platform to study the dynamics of MuSCs and their interaction with nonmyogenic cells during muscle regeneration. Using three-dimensional time-lapse imaging on live reporter mice and taking advantages of the autofluorescence of reduced nicotinamide adenine dinucleotide (NADH), we studied the spatiotemporal interaction between nonmyogenic cells and muscle stem/progenitor cells during MuSC activation and proliferation. We discovered that their cell-cell contact was transient in nature. Moreover, MuSCs could activate with notably reduced infiltration of neutrophils and macrophages, and their proliferation, although dependent on macrophages, did not require constant contact with them. These findings provide a fresh perspective on myeloid cells’ role during muscle regeneration. American Association for the Advancement of Science 2023-10-18 /pmc/articles/PMC10584350/ /pubmed/37851799 http://dx.doi.org/10.1126/sciadv.adi1891 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
He, Yingzhu
Heng, Youshan
Qin, Zhongya
Wei, Xiuqing
Wu, Zhenguo
Qu, Jianan
Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title_full Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title_fullStr Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title_full_unstemmed Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title_short Intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
title_sort intravital microscopy of satellite cell dynamics and their interaction with myeloid cells during skeletal muscle regeneration
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584350/
https://www.ncbi.nlm.nih.gov/pubmed/37851799
http://dx.doi.org/10.1126/sciadv.adi1891
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