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ARS Home » Plains Area » Houston, Texas » Children's Nutrition Research Center » Research » Publications at this Location » Publication #212278
Title: The circadian modulation of leptin-controlled bone formation

Author
item Fu, Loning
item PATEL, M - BAYLOR COLLEGE MED
item Karsenty, Gerald

Submitted to: Book Chapter
Publication Type: Book / Chapter
Publication Acceptance Date: 6/20/2006
Publication Date: 7/27/2006
Citation: Fu, L., Patel, M.S., Karsenty, G. 2006. The circadian modulation of leptin-controlled bone formation. In: Kalsbeek, A., Fliers, E., Hofman, M.A., Swaab, D.F., van Someren, E.J.W., Buijs, R. M., editors. Progress in Brain Research. Amsterdam, The Netherlands: Elsevier. p. 153:177-188.

Interpretive Summary:

Technical Abstract: Mice with circadian gene Period and Cryptochrome mutations develop high bone mass early in life. Such a phenotype is accompanied by an increase in osteoblast numbers in mutant bone and cannot be corrected by leptin intracerebroventricular infusion. Thus, the molecular clock plays a key role in leptin-mediated sympathetic regulation of bone formation. Indeed, we found that leptin-dependent sympathetic signaling induces the expression of AP1 and circadian genes in bone and in osteoblasts with similar kinetics, and these two pathways play opposite roles in controlling c-myc expression. Mutations in the Period 1 and 2 genes result in uncontrolled c-myc signaling, overexpression of G1 cyclins, and increased osteoblast proliferation and bone-formation parameters. These results indicate that the role of leptin-dependent sympathetic signaling in bone formation is achieved through regulating two antagonistic pathways in osteoblasts.