Single Stem Cell Imaging and Analysis Reveals Telomere Length Differences in Diseased Human and Mouse Skeletal Muscles.
Single Stem Cell Imaging and Analysis Reveals Telomere Length Differences in Diseased Human and Mouse Skeletal Muscles.
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DOI:
10.1016/j.stemcr.2017.08.003
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发表时间:
2017-10-10
影响因子:
5.9
通讯作者:
Mourkioti F
中科院分区:
文献类型:
--
作者:
Tichy ED;Sidibe DK;Tierney MT;Stec MJ;Sharifi-Sanjani M;Hosalkar H;Mubarak S;Johnson FB;Sacco A;Mourkioti F
Muscle stem cells (MuSCs) contribute to muscle regeneration following injury. In many muscle disorders, the repeated cycles of damage and repair lead to stem cell dysfunction. While telomere attrition may contribute to aberrant stem cell functions, methods to accurately measure telomere length in stem cells from skeletal muscles have not been demonstrated. Here, we have optimized and validated such a method, named MuQ-FISH, for analyzing telomere length in MuSCs from either mice or humans. Our analysis showed no differences in telomere length between young and aged MuSCs from uninjured wild-type mice, but MuSCs isolated from young dystrophic mice exhibited significantly shortened telomeres. In corroboration, we demonstrated that telomere attrition is present in human dystrophic MuSCs, which underscores its importance in diseased regenerative failure. The robust technique described herein provides analysis at a single-cell resolution and may be utilized for other cell types, especially rare populations of cells. MuQ-FISH is a telomere analysis assay of mouse and human muscle stem cells Highly sensitive telomere analysis on small numbers of cells Detection of both telomere length and number of telomere foci with MuQ-FISH assay Telomere analysis is now possible in quiescent and/or cycling stem cells In this article, Mourkioti and colleagues develop a telomere assay named MuQ-FISH and show that the critical telomere shortening of muscle stem cells from boys with Duchenne muscular dystrophy contributes to the progressive dysfunction that compromises their regenerative potential.
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影响因子:
64.8
作者:
Batista, Luis F. Z.;Pech, MatthewF.;Zhong, Franklin L.;Nguyen, Ha Nam;Xie, Kathleen T.;Zaug, Arthur J.;Crary, Sharon M.;Choi, Jinkuk;Sebastiano, Vittorio;Cherry, Athena;Giri, Neelam;Wernig, Marius;Alter, Blanche P.;Cech, Thomas R.;Savage, Sharon A.;Pera, Renee A. Reijo;Artandi, Steven E.
通讯作者:
Artandi, Steven E.
DOI:
10.1083/jcb.134.1.1
发表时间:
1996-07
期刊:
The Journal of cell biology
影响因子:
--
作者:
Henderson S;Allsopp R;Spector D;Wang SS;Harley C
通讯作者:
Harley C
影响因子:
2.8
作者:
Decary, S;Ben Hamida, C;Butler-Browne, GS
通讯作者:
Butler-Browne, GS
影响因子:
4
作者:
HARLEY, CB;VILLEPONTEAU, B
通讯作者:
VILLEPONTEAU, B
影响因子:
82.9
作者:
Dumont NA;Wang YX;von Maltzahn J;Pasut A;Bentzinger CF;Brun CE;Rudnicki MA
通讯作者:
Rudnicki MA