Parathyroid hormone (PTH) receptors and the biological response to PTH in osteoblasts have been shown to be influenced by glucocorticoids, growth factors, cytokines or PTH itself. Furthermore, components of extracellular matrix (ECM) appear to regulate the response to PTH as well. We investigated th
Parathyroid hormone (1–34) regulates integrin expression in vivo in rat osteoblasts
✍ Scribed by Edelgard Kaiser; Masahiko Sato; Jude E. Onyia; Srinivasan Chandrasekhar
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 646 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0730-2312
- DOI
- 10.1002/jcb.1256
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✦ Synopsis
Intermittent administration of parathyroid hormone (PTH) activates new sites of bone formation by stimulating osteoblast differentiation and function resulting in an increase in bone mass. Because integrins have been shown to play a crucial role in osteoblast differentiation and bone formation, in the present study, we evaluated whether human PTH (1±34) upon administration to rats, in¯uenced integrin expression in osteoblastic cells isolated from the metaphysis and the diaphysis of rat long bones. Initial immunohistochemical evaluation of bone sections demonstrated that the osteoblasts expressed at least a v , a 2 , a 3 , and a 5 b 1 integrins. Immunocolocalization studies for integrins and vinculin established that a v , a 2 , and a 5 b 1 , but not a 3 integrins were present in the focal adhesion sites of osteoblasts attached to FN coated surfaces. Osteoprogenitor cells isolated from metaphyseal (but not diaphyseal) marrow of rats injected with intermittent PTH (1±34) exhibited greater a v and reduced a 2 levels, with no apparent changes in a 3 , and a 5 b 1 integrin levels, as assessed by immunohistochemistry, Northern, and Western blot analyses. However, these changes were not observed on the same cells treated with PTH in vitro. These observations suggest that integrin modulation by PTH is likely to be indirect and that selective phenotypic expression of integrin subtypes is part of te cascade of events that lead to PTH (1±34) mediated osteoblast differentiation.
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