Počet záznamů: 1
BMP Signaling Regulates the Fate of Chondro-osteoprogenitor Cells in Facial Mesenchyme in a Stage-Specific Manner
- 1.0468150 - ÚŽFG 2017 RIV US eng J - Článek v odborném periodiku
Celá, Petra - Buchtová, Marcela - Veselá, Iva - Fu, K. - Bogardi, J. P. - Song, Y. - Barlow, A. - Buxton, P. - Medalová, J. - Francis-West, P. - Richman, J. M.
BMP Signaling Regulates the Fate of Chondro-osteoprogenitor Cells in Facial Mesenchyme in a Stage-Specific Manner.
Developmental Dynamics. Roč. 245, č. 9 (2016), s. 947-962. ISSN 1058-8388. E-ISSN 1097-0177
Grant CEP: GA ČR GA304/09/0725; GA ČR GB14-37368G
Institucionální podpora: RVO:67985904
Klíčová slova: noggin * chicken embryo * cartilage
Kód oboru RIV: EA - Morfologické obory a cytologie
Impakt faktor: 2.004, rok: 2016
DOI: https://doi.org/10.1002/DVDY.24422
Background: Lineage tracing has shown that most of the facial skeleton is derived from cranial neural crest cells. However, the local signals that influence postmigratory, neural crest-derived mesenchyme also play a major role in patterning the skeleton. Here, we study the role of BMP signaling in regulating the fate of chondro-osteoprogenitor cells in the face. Results: A single Noggin-soaked bead inserted into stage 15 chicken embryos induced an ectopic cartilage resembling the interorbital septum within the palate and other midline structures. In contrast, the same treatment in stage 20 embryos caused a loss of bones. The molecular basis for the stage-specific response to Noggin lay in the simultaneous up-regulation of SOX9 and downregulation of RUNX2 in the maxillary mesenchyme, increased cell adhesiveness as shown by N-cadherin induction around the beads and increased RA pathway gene expression. None of these changes were observed in stage 20 embryos. Conclusions: These experiments demonstrate how slight changes in expression of growth factors such as BMPs could lead to gain or loss of cartilage in the upper jaw during vertebrate evolution. In addition, BMPs have at least two roles: one in patterning the skull and another in regulating the skeletogenic fates of neural crest-derived mesenchyme.
Trvalý link: http://hdl.handle.net/11104/0266008
Počet záznamů: 1