TY - JOUR
T1 - A transitional extracellular matrix instructs cell behavior during muscle regeneration
AU - Calve, Sarah
AU - Odelberg, Shannon J.
AU - Simon, Hans Georg
N1 - Funding Information:
The authors thank Dr. E. Amaya for sharing the pXCarGFP3 reporter plasmid. We are grateful to Dr. C. Huppenbauer and M. Tjepkema of W. Nuhsbaum Inc., N. Swentko of Intavis Inc., and Donald Atkinson for expert technical support. In addition, we would like to thank S. Mercer, Drs. R. Sadleir and L. Larkin for critical reading of the manuscript, and all members of the Simon laboratory for helpful discussions. This work was supported by DARPA , Restorative Injury Repair BAA04-12 Addendum B (H.-G. Simon and S. Odelberg), Searle Funds at The Chicago Community Trust (H.-G. Simon), and NIH T90 Regenerative Medicine Training Program (S. Calve).
PY - 2010/8/1
Y1 - 2010/8/1
N2 - Urodele amphibians regenerate appendages through the recruitment of progenitor cells into a blastema that rebuilds the lost tissue. Blastemal formation is accompanied by extensive remodeling of the extracellular matrix. Although this remodeling process is important for appendage regeneration, it is not known whether the remodeled matrix directly influences the generation and behavior of blastemal progenitor cells. By integrating in vivo 3-dimensional spatiotemporal matrix maps with in vitro functional time-lapse imaging, we show that key components of this dynamic matrix, hyaluronic acid, tenascin-C and fibronectin, differentially direct cellular behaviors including DNA synthesis, migration, myotube fragmentation and myoblast fusion. These data indicate that both satellite cells and fragmenting myofibers contribute to the regeneration blastema and that the local extracellular environment provides instructive cues for the regenerative process. The fact that amphibian and mammalian myoblasts exhibit similar responses to various matrices suggests that the ability to sense and respond to regenerative signals is evolutionarily conserved.
AB - Urodele amphibians regenerate appendages through the recruitment of progenitor cells into a blastema that rebuilds the lost tissue. Blastemal formation is accompanied by extensive remodeling of the extracellular matrix. Although this remodeling process is important for appendage regeneration, it is not known whether the remodeled matrix directly influences the generation and behavior of blastemal progenitor cells. By integrating in vivo 3-dimensional spatiotemporal matrix maps with in vitro functional time-lapse imaging, we show that key components of this dynamic matrix, hyaluronic acid, tenascin-C and fibronectin, differentially direct cellular behaviors including DNA synthesis, migration, myotube fragmentation and myoblast fusion. These data indicate that both satellite cells and fragmenting myofibers contribute to the regeneration blastema and that the local extracellular environment provides instructive cues for the regenerative process. The fact that amphibian and mammalian myoblasts exhibit similar responses to various matrices suggests that the ability to sense and respond to regenerative signals is evolutionarily conserved.
KW - 3D imaging
KW - Extracellular matrix
KW - Limb regeneration
KW - Newt
KW - Skeletal muscle progenitor cells
KW - Time-lapse microscopy
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U2 - 10.1016/j.ydbio.2010.05.007
DO - 10.1016/j.ydbio.2010.05.007
M3 - Article
C2 - 20478295
AN - SCOPUS:77955054674
SN - 0012-1606
VL - 344
SP - 259
EP - 271
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -