BMP action in skeletogenesis involves attenuation of retinoid signaling

被引:92
作者
Hoffman, Lisa M.
Garcha, Kamal
Karamboulas, Konstantina
Cowan, Matthew F.
Drysdale, Linsay M.
Horton, William A.
Underhill, T. Michael [1 ]
机构
[1] Univ Western Ontario, Dept Physiol, Fad Med & Dent, London, ON N6A 5C1, Canada
[2] Univ British Columbia, Dept Cellular & Physiol Sci, Vancouver, BC V6T 1Z3, Canada
[3] Shriners Hosp Children, Portland, OR 97239 USA
关键词
D O I
10.1083/jcb.200604150
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
he bone morphogenetic protein (BMP) and growth and differentiation factor (GDF) signaling pathways have well-established and essential roles within the developing skeleton in coordinating the formation of cartilaginous anlagen. However, the identification of bona. de targets that underlie the action of these signaling molecules in chondrogenesis has remained elusive. We have identified the gene for the retinoic acid ( RA) synthesis enzyme Aldh1a2 as a principal target of BMP signaling; prochondrogenic BMPs or GDFs lead to attenuation of Aldh1a2 expression and, consequently, to reduced activation of the retinoid signaling pathway. Consistent with this, antagonism of retinoid signaling phenocopies BMP4 action, whereas RA inhibits the chondrogenic stimulatory activity of BMP4. BMP4 also down-regulates Aldh1a2 expression in organ culture and, consistent with this, Aldh1a2 is actively excluded from the developing cartilage anlagens. Collectively, these findings provide novel insights into BMP action and demonstrate that BMP signaling governs the fate of prechondrogenic mesenchyme, at least in part, through regulation of retinoid signaling.
引用
收藏
页码:101 / 113
页数:13
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