Connexin43 regulates joint location in zebrafish fins
Joints are essential for skeletal form and function, yet their development remains poorly understood. In zebrafish fins, joints form between the bony fin ray segments providing essentially unlimited opportunities to evaluate joint morphogenesis. Mutations in cx43 cause the short segment phenotype of...
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Veröffentlicht in: | Developmental biology 2009-03, Vol.327 (2), p.410-418 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Joints are essential for skeletal form and function, yet their development remains poorly understood. In zebrafish fins, joints form between the bony fin ray segments providing essentially unlimited opportunities to evaluate joint morphogenesis. Mutations in
cx43 cause the short segment phenotype of
short fin (
sof
b123
) mutants, suggesting that direct cell–cell communication may regulate joint location. Interestingly, increased
cx43 expression in the
another long fin (
alf
dty86
) mutant appears to cause joint failure typical of that mutant. Indeed, knockdown of
cx43 in
alf
dty86
mutant fins rescues joint formation. Together, these data reveal a correlation between the level of Cx43 expression in the fin ray mesenchyme and the location of joints. Cx43 was also observed laterally in cells associated with developing joints. Confocal microscopy revealed that the Cx43 protein initially surrounds the membranes of ZNS5-positive joint cells, but at later stages becomes polarized toward the underlying Cx43-positive mesenchymal cells. One possibility is that communication between the Cx43-positive mesenchyme and the overlying ZNS5-positive cells regulates joint location, and upregulation of Cx43 in joint-forming cells contributes to joint morphogenesis. |
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ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/j.ydbio.2008.12.027 |