期刊
PLOS ONE
卷 12, 期 11, 页码 -出版社
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0187980
关键词
-
资金
- National Institute of Health/National Institute of Arthritis and Musculoskeletal and Skin Diseases [R01-AR041255, P30-R057235]
- Barnes Jewish Hospital Foundation
Connexin43 (Cx43) is the main gap junction protein expressed in bone forming cells, where it modulates peak bone mass acquisition and cortical modeling. Genetic ablation of the Cx43 gene (Gja1) results in cortical expansion with accentuated periosteal bone formation associated with decreased expression of the Wnt inhibitor sclerostin. To determine whether sclerostin (Sost) down-regulation might contribute to periosteal expansion in Gja1 deficient bones, we took a gene interaction approach and crossed mice harboring germline null alleles for Gja1 or Sost to generate single Gja1(+/-) and Sost(+/-) and double Gja1(+/-); Sost(+/-) heterozygous mice. In vivo mu CT analysis of cortical bone at age 1 and 3 months confirmed increased thickness in Sost(-/-) mice, but revealed no cortical abnormalities in single Gja1(+/-) or Sost(+/-) mice. Double heterozygous Gja1(+/-) Sost(+/-) also showed no differences in mineral density, cortical thickness, width or geometry relative to wild type control mice. Likewise, 3-point bending measurement of bone strength revealed no significant differences between double Gja1(+/-); Sost(+/-) or single heterozygous and wild type mice. Although these data do not exclude a contribution of reduced sclerostin in the cortical expansion seen in Gja1 deficient bones, they are not consistent with a strong genetic interaction between Sost and Gja1 dictating cortical modeling.
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