Three-dimensional imaging studies in mice identify cellular dynamics of skeletal muscle regeneration

被引:11
作者
Collins, Brittany C. [1 ,3 ]
Shapiro, Jacob B. [1 ,4 ]
Scheib, Mya M. [1 ]
Musci, Robert V. [1 ,5 ]
Verma, Mayank [2 ]
Kardon, Gabrielle [1 ]
机构
[1] Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
[2] Univ Texas Southwestern Med Ctr, Dept Pediat, Div Neurol, Dallas, TX USA
[3] BioFire Def, Murray, UT USA
[4] Univ Wisconsin, Sch Med & Publ Hlth, Dept Anesthesiol, Madison, WI USA
[5] Loyola Marymount Univ, Frank R Seaver Coll Sci & Engn, Dept Hlth & Human Sci, Los Angeles, CA USA
关键词
DYSTROPHIC MDX MUSCLE; TEMPLATE DNA STRANDS; SATELLITE CELLS; STEM-CELLS; BRANCHED FIBERS; HISTOPATHOLOGICAL CHANGES; MUSCULAR-DYSTROPHY; PRECURSOR CELLS; BASAL LAMINA; IN-VIVO;
D O I
10.1016/j.devcel.2024.03.017
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The function of many organs, including skeletal muscle, depends on their three-dimensional structure. Muscle regeneration therefore requires not only reestablishment of myofibers but also restoration of tissue architecture. Resident muscle stem cells (SCs) are essential for regeneration, but how SCs regenerate muscle architecture is largely unknown. We address this problem using genetic labeling of mouse SCs and whole -mount imaging to reconstruct, in three dimensions, muscle regeneration. Unexpectedly, we found that myofibers form via two distinct phases of fusion and the residual basement membrane of necrotic myofibers is critical for promoting fusion and orienting regenerated myofibers. Furthermore, the centralized myonuclei characteristic of regenerated myofibers are associated with myofibrillogenesis and endure months post injury. Finally, we elucidate two cellular mechanisms for the formation of branched myofibers, a pathology characteristic of diseased muscle. We provide a synthesis of the cellular events of regeneration and show that these differ from those used during development.
引用
收藏
页码:1457 / 1474.e5
页数:24
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