Journal article
Bone homeostasis in growth hormone receptor-null mice is restored by IGF-I but independent of Stat5
NA Sims, P Clément-Lacroix, F Da Ponte, Y Bouali, N Binart, R Moriggl, V Goffin, K Coschigano, M Gaillard-Kelly, J Kopchick, R Baron, PA Kelly
Journal of Clinical Investigation | AMER SOC CLINICAL INVESTIGATION INC | Published : 2000
DOI: 10.1172/JCI10753
Abstract
Growth hormone (GH) regulates both bone growth and remodeling, but it is unclear whether these actions are mediated directly by the GH receptor (GHR) and/or IGF-I signaling. The actions of GH are transduced by the Jak/Stat signaling pathway via Stat5, which is thought to regulate IGF-I expression. To determine the respective roles of GHR and IGF-I in bone growth and remodeling, we examined bones of wild-type, GHR knockout (GHR(-/-)), Stat5ab(-/-), and GHR(-/-) mice treated with IGF-I. Reduced bone growth in GHR(-/-) mice, due to a premature reduction in chondrocyte proliferation and cortical bone growth, was detected after 2 weeks of age. Additionally, although trabecular bone volume was unc..
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Awarded by National Institute of Dental and Craniofacial Research