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Publication : Enhanced prostacyclin formation and Wnt signaling in sclerostin deficient osteocytes and bone.

First Author  Ryan ZC Year  2014
Journal  Biochem Biophys Res Commun Volume  448
Issue  1 Pages  83-8
PubMed ID  24780398 Mgi Jnum  J:219447
Mgi Id  MGI:5620844 Doi  10.1016/j.bbrc.2014.04.092
Citation  Ryan ZC, et al. (2014) Enhanced prostacyclin formation and Wnt signaling in sclerostin deficient osteocytes and bone. Biochem Biophys Res Commun 448(1):83-8
abstractText  We show that prostacyclin production is increased in bone and osteocytes from sclerostin (Sost) knockout mice which have greatly increased bone mass. The addition of prostacyclin or a prostacyclin analog to bone forming osteoblasts enhances differentiation and matrix mineralization of osteoblasts. The increase in prostacyclin synthesis is linked to increases in beta-catenin concentrations and activity as shown by enhanced binding of lymphoid enhancer factor, Lef1, to promoter elements within the prostacyclin synthase promoter. Blockade of Wnt signaling reduces prostacyclin production in osteocytes. Increased prostacyclin production by osteocytes from sclerostin deficient mice could potentially contribute to the increased bone formation seen in this condition.
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