TY - JOUR
T1 - Muscle contraction controls skeletal morphogenesis through regulation of chondrocyte convergent extension
AU - Shwartz, Yulia
AU - Farkas, Zsuzsanna
AU - Stern, Tomer
AU - Aszódi, Attila
AU - Zelzer, Elazar
N1 - Israel Science Foundation (ISF) [1206/09]; Minerva Foundation [M1138]; The Y. Leon Benoziyo Institute for Molecular Medicine; Helen and Martin Kimmel Institute for Stem Cell Research; J&R Center for Scientific Research; Estate of Raymond Lapon; Estate of David Levinson; The Leo and Julia Forchheimer Center for Molecular Genetics; Marla L. Schaefer, New York, NY, USAThis work was supported by grants from the Israel Science Foundation (ISF, Grants 1206/09), Minerva Foundation (Grant M1138), The Y. Leon Benoziyo Institute for Molecular Medicine, Helen and Martin Kimmel Institute for Stem Cell Research, J&R Center for Scientific Research, Estate of Raymond Lapon, Estate of David Levinson, The Leo and Julia Forchheimer Center for Molecular Genetics, and Marla L. Schaefer, New York, NY, USA. E.Z. is the incumbent of the Martha S. Sagon Career Development Chair.
PY - 2012/10/1
Y1 - 2012/10/1
N2 - Convergent extension driven by mediolateral intercalation of chondrocytes is a key process that contributes to skeletal growth and morphogenesis. While progress has been made in deciphering the molecular mechanism that underlies this process, the involvement of mechanical load exerted by muscle contraction in its regulation has not been studied. Using the zebrafish as a model system, we found abnormal pharyngeal cartilage morphology in both chemically and genetically paralyzed embryos, demonstrating the importance of muscle contraction for zebrafish skeletal development. The shortening of skeletal elements was accompanied by prominent changes in cell morphology and organization. While in control the cells were elongated, chondrocytes in paralyzed zebrafish were smaller and exhibited a more rounded shape, confirmed by a reduction in their length-to-width ratio. The typical columnar organization of cells was affected too, as chondrocytes in various skeletal elements exhibited abnormal stacking patterns, indicating aberrant intercalation. Finally, we demonstrate impaired chondrocyte intercalation in growth plates of muscle-less Spd mouse embryos, implying the evolutionary conservation of muscle force regulation of this essential morphogenetic process.Our findings provide a new perspective on the regulatory interaction between muscle contraction and skeletal morphogenesis by uncovering the role of muscle-induced mechanical loads in regulating chondrocyte intercalation in two different vertebrate models.
AB - Convergent extension driven by mediolateral intercalation of chondrocytes is a key process that contributes to skeletal growth and morphogenesis. While progress has been made in deciphering the molecular mechanism that underlies this process, the involvement of mechanical load exerted by muscle contraction in its regulation has not been studied. Using the zebrafish as a model system, we found abnormal pharyngeal cartilage morphology in both chemically and genetically paralyzed embryos, demonstrating the importance of muscle contraction for zebrafish skeletal development. The shortening of skeletal elements was accompanied by prominent changes in cell morphology and organization. While in control the cells were elongated, chondrocytes in paralyzed zebrafish were smaller and exhibited a more rounded shape, confirmed by a reduction in their length-to-width ratio. The typical columnar organization of cells was affected too, as chondrocytes in various skeletal elements exhibited abnormal stacking patterns, indicating aberrant intercalation. Finally, we demonstrate impaired chondrocyte intercalation in growth plates of muscle-less Spd mouse embryos, implying the evolutionary conservation of muscle force regulation of this essential morphogenetic process.Our findings provide a new perspective on the regulatory interaction between muscle contraction and skeletal morphogenesis by uncovering the role of muscle-induced mechanical loads in regulating chondrocyte intercalation in two different vertebrate models.
UR - http://www.scopus.com/inward/record.url?scp=84865652711&partnerID=8YFLogxK
U2 - 10.1016/j.ydbio.2012.07.026
DO - 10.1016/j.ydbio.2012.07.026
M3 - مقالة
SN - 0012-1606
VL - 370
SP - 154
EP - 163
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -