Abstract:
:Glucose-dependent insulinotropic peptide (GIP) is a 42-amino acid peptide synthesized and secreted from endocrine cells in the small intestine. The role of GIP in coupling nutrient intake and insulin secretion, the incretin effect, is well known. We report that GIP receptor messenger RNA and protein are present in normal bone and osteoblast-like cell lines, and that high affinity receptors for GIP can be demonstrated by [125I]GIP binding studies. When applied to osteoblast-like cells (SaOS2), GIP stimulated increases in cellular cAMP content and intracellular calcium, with both responses being dose dependent. Moreover, administration of GIP results in elevated expression of collagen type I messenger RNA as well as an increase in alkaline phosphatase activity. Both of these effects reflect anabolic actions of presumptive osteoblasts. These results provide the first evidence that GIP receptors are present in bone and osteoblast-like cells and that GIP modulates the function of these cells.
journal_name
Endocrinologyjournal_title
Endocrinologyauthors
Bollag RJ,Zhong Q,Phillips P,Min L,Zhong L,Cameron R,Mulloy AL,Rasmussen H,Qin F,Ding KH,Isales CMdoi
10.1210/endo.141.3.7366subject
Has Abstractpub_date
2000-03-01 00:00:00pages
1228-35issue
3eissn
0013-7227issn
1945-7170journal_volume
141pub_type
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