dc.contributorColumbia Univ
dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorYadav, Vijay K.
dc.creatorArantes, Henrique Pierotti [UNIFESP]
dc.creatorBarros, Elizabete Ribeiro [UNIFESP]
dc.creatorLazaretti-Castro, Marise [UNIFESP]
dc.creatorDucy, Patricia
dc.date.accessioned2016-01-24T13:59:38Z
dc.date.available2016-01-24T13:59:38Z
dc.date.created2016-01-24T13:59:38Z
dc.date.issued2010-05-01
dc.identifierCalcified Tissue International. New York: Springer, v. 86, n. 5, p. 382-388, 2010.
dc.identifier0171-967X
dc.identifierhttp://repositorio.unifesp.br/handle/11600/32501
dc.identifier10.1007/s00223-010-9350-7
dc.identifierWOS:000277014000007
dc.description.abstractThe low-density lipoprotein receptor-related protein (Lrp)-5 regulates osteoblast proliferation and bone formation through its expression in duodenum by modifying the gut serotonin-bone endocrine axis. However, its direct role, if any, in osteoblast progenitor cells has not been studied thus far. Here, we show that mice with a Dermo1-Cre-mediated disruption of Lrp5 in osteoblast progenitor cells have normal embryonic skeletogenesis and normal skeletal growth and development postnatally. Histomorphometric analysis of 3-month-old adult mice revealed normal osteoblast numbers, bone formation rate, and bone mass in Lrp5 (Dermo) (-/-) mice. in addition, analysis of two osteoporosis pseudoglioma (OPPG) patients revealed a three- to fivefold increase in their serum serotonin levels compared to age-matched controls. These results rule out a direct function of Lrp5 in osteoblast progenitor cells and add further support to the notion that dysregulation of serotonin synthesis is involved in bone mass abnormalities observed in OPPG patients.
dc.languageeng
dc.publisherSpringer
dc.relationCalcified Tissue International
dc.rightshttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dc.rightsAcesso restrito
dc.subjectOsteoblast
dc.subjectOsteoporosis
dc.subjectAnimal model
dc.subjectMouse genetics/transgenics
dc.titleGenetic Analysis of Lrp5 Function in Osteoblast Progenitors
dc.typeArtigo


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