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      Intravital Imaging Reveals Ghost Fibers as Architectural Units Guiding Myogenic Progenitors During Regeneration

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          Summary

          How resident stem cells and their immediate progenitors rebuild tissues of pre-injury organization and size for proportional regeneration is not well understood. Using 3D, time-lapse intravital imaging for direct visualization of the muscle regeneration process in live mice, we report that extra-cellular matrix remnants from injured skeletal muscle fibers, “ghost fibers,” govern muscle stem/progenitor cell behaviors during proportional regeneration. Stem cells were immobile and quiescent without injury whereas their activated progenitors migrated and divided after injury. Unexpectedly, divisions and migration were primarily bi-directionally oriented along the ghost fiber longitudinal axis, allowing for spreading of progenitors throughout ghost fibers. Re-orienting ghost fibers impacted myogenic progenitors’ migratory paths and division planes, causing disorganization of regenerated muscle fibers. We conclude that ghost fibers are autonomous, architectural units necessary for proportional regeneration after tissue injury. This finding reinforces the need to fabricate bioengineered matrices that mimic living tissue matrices for tissue regeneration therapy.

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          Journal
          101311472
          34100
          Cell Stem Cell
          Cell Stem Cell
          Cell stem cell
          1934-5909
          1875-9777
          12 November 2015
          10 December 2015
          4 February 2016
          04 February 2017
          : 18
          : 2
          : 243-252
          Affiliations
          [1 ]Department of Embryology, Carnegie Institution of Washington, 3520 San Martin Drive, Baltimore, MD 21218
          [2 ]Cell Biology and Metabolism Branch, Eunice Kennedy Shriver National Institutes of Child Health and Human Development, National Institute of Health, Building 35A, 9000 Rockville Pike, Bethesda, MD 20892
          Author notes
          Article
          PMC4744135 PMC4744135 4744135 nihpa737011
          10.1016/j.stem.2015.11.005
          4744135
          26686466
          d20710d8-b878-4e13-b529-a604d7bfe408
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