TY - JOUR
T1 - Tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest
AU - Cheah, Felicia S.H.
AU - Winkler, Christoph
AU - Jabs, Ethylin Wang
AU - Chong, Samuel S.
N1 - Funding Information:
We thank Vladimir Korzh (Institute of Molecular and Cell Biology, Singapore) for invaluable advice, technical support and the gift of the foxd3 probe, Yi-Lin Yan and Monte Westerfield (University of Oregon, Eugene, OR) for gifts of the sox9a and dlx2a probes, respectively, Paul A. Krieg (University of Arizona College of Medicine, Tucson, AZ) for the gift of the pT7TS expression vector, and Jin Ben and Gare Hoon Yeo for technical assistance. This work was supported by grants from the National University of Singapore Academic Research Fund (R-178-000-104-112) and Biomedical Research Council of Singapore to SSC (BMRC 06/1/21/19/459) and CW (BMRC 07/1/21/19/544).
PY - 2010/7
Y1 - 2010/7
N2 - Zebrafish tgfβ3 is strongly expressed in a subpopulation of the migrating neural crest cells, developing pharyngeal arches and neurocranial cartilages. To study the regulatory role of tgfβ3 in head skeletal formation, we knocked down tgfβ3 in zebrafish and found impaired craniofacial chondrogenesis, evident by malformations in selected neurocranial and pharyngeal arch cartilages. Over-expressing tgfβ3 in embryos resulted in smaller craniofacial cartilages without any gross malformations. These defects suggest that tgfβ3 is required for normal chondrogenesis. To address the cellular mechanisms that lead to the observed malformations, we analyzed cranial neural crest development in morphant and tgfβ3 over-expressing fish. We observed reduced pre-migratory and migratory cranial neural crest, the precursors of the neurocranial cartilage and pharyngeal arches, in tgfβ3 knockdown embryos. In contrast, only the migratory neural crest was reduced in embryos over-expressing tgfβ3. This raised the possibility that the reduced number of cranial neural crest cells is a result of increased apoptosis. Consistent with this, markedly elevated TUNEL staining in the midbrain and hindbrain, and developing pharyngeal arch region was observed in morphants, while tgfβ3 over-expressing embryos showed marginally increased apoptosis in the developing pharyngeal arch region. We propose that both Tgfβ3 suppression and over-expression result in reduced chondrocyte and osteocyte formation, but to different degrees and through different mechanisms. In Tgfβ3 suppressed embryos, this is due to impaired formation and survival of a subpopulation of cranial neural crest cells through markedly increased apoptosis in regions containing the cranial neural crest cells, while in Tgfβ3 over-expressing embryos, the milder phenotype is also due to a slightly elevated apoptosis in these regions. Therefore, proper cranial neural crest formation and survival, and ultimately craniofacial chondrogenesis and osteogenesis, are dependent on tight regulation of Tgfβ3 protein levels in zebrafish.
AB - Zebrafish tgfβ3 is strongly expressed in a subpopulation of the migrating neural crest cells, developing pharyngeal arches and neurocranial cartilages. To study the regulatory role of tgfβ3 in head skeletal formation, we knocked down tgfβ3 in zebrafish and found impaired craniofacial chondrogenesis, evident by malformations in selected neurocranial and pharyngeal arch cartilages. Over-expressing tgfβ3 in embryos resulted in smaller craniofacial cartilages without any gross malformations. These defects suggest that tgfβ3 is required for normal chondrogenesis. To address the cellular mechanisms that lead to the observed malformations, we analyzed cranial neural crest development in morphant and tgfβ3 over-expressing fish. We observed reduced pre-migratory and migratory cranial neural crest, the precursors of the neurocranial cartilage and pharyngeal arches, in tgfβ3 knockdown embryos. In contrast, only the migratory neural crest was reduced in embryos over-expressing tgfβ3. This raised the possibility that the reduced number of cranial neural crest cells is a result of increased apoptosis. Consistent with this, markedly elevated TUNEL staining in the midbrain and hindbrain, and developing pharyngeal arch region was observed in morphants, while tgfβ3 over-expressing embryos showed marginally increased apoptosis in the developing pharyngeal arch region. We propose that both Tgfβ3 suppression and over-expression result in reduced chondrocyte and osteocyte formation, but to different degrees and through different mechanisms. In Tgfβ3 suppressed embryos, this is due to impaired formation and survival of a subpopulation of cranial neural crest cells through markedly increased apoptosis in regions containing the cranial neural crest cells, while in Tgfβ3 over-expressing embryos, the milder phenotype is also due to a slightly elevated apoptosis in these regions. Therefore, proper cranial neural crest formation and survival, and ultimately craniofacial chondrogenesis and osteogenesis, are dependent on tight regulation of Tgfβ3 protein levels in zebrafish.
KW - Apoptosis
KW - Chondrogenesis
KW - Cranial neural crest
KW - Differentiation
KW - Neurocranial cartilage
KW - Osteogenesis
KW - Pharyngeal arch
KW - Proliferation
KW - Survival
KW - Tgfβ3
UR - http://www.scopus.com/inward/record.url?scp=77953610192&partnerID=8YFLogxK
U2 - 10.1016/j.mod.2010.04.003
DO - 10.1016/j.mod.2010.04.003
M3 - Article
C2 - 20406684
AN - SCOPUS:77953610192
SN - 0925-4773
VL - 127
SP - 329
EP - 344
JO - Mechanisms of Development
JF - Mechanisms of Development
IS - 7-8
ER -