Ghrelin directly regulates bone formation

被引:230
作者
Fukushima, N
Hanada, R
Teranishi, H
Fukue, Y
Tachibana, T
Ishikawa, H
Takeda, S
Takeuchi, Y
Fukumoto, S
Kangawa, K
Nagata, K
Kojima, M
机构
[1] Kurume Univ, Inst Life Sci, Kurume, Fukuoka 8390861, Japan
[2] Kurume Univ, Sch Med, Dept Orthoped Surg, Kurume, Fukuoka 830, Japan
[3] Jikei Univ, Daisan Hosp, Sch Med, Dept Anat,Minato Ku, Tokyo 201, Japan
[4] Tokyo Med & Dent Univ, Grad Sch, Ctr Excellence,Sect Orthoped & Spinal Surg, Program Frontier Res Mol Destruct & Reconstruct T, Tokyo, Japan
[5] Toranomon Gen Hosp, Dept Endocrinol & Metab, Minato Ku, Tokyo, Japan
[6] Tokyo Univ Hosp, Dept Internal Med, Div Nephrol & Endocrinol, Bunkyo Ku, Tokyo 113, Japan
[7] Natl Cardiovasc Ctr, Res Inst, Dept Biochem, Suita, Osaka 565, Japan
关键词
ghrelin; growth hormone secretagogue receptor 1a; osteoblast; differentiation; BMD;
D O I
10.1359/JBMR.041237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To clarify the role of ghrelin in bone metabolism, we examined the effect of ghrelin in vitro and in vivo. Ghrelin and its receptor, GHS-R1a, were identified in osteoblasts, and ghrelin promoted both proliferation and differentiation. Furthermore, ghrelin increased BMD in rats. Our results show that ghrelin directly affects bone formation. Introduction: Ghrelin is a gut peptide involved in growth hormone (GH) secretion and energy homeostasis. Recently, it has been reported that the adipocyte-derived hormone leptin, which also regulates energy homeostasis and opposes ghrelin's actions in energy homeostasis, plays a significant role in bone metabolism. This evidence implies that ghrelin may modulate bone metabolism; however, it has not been clarified. To study the role of ghrelin in skeletal integrity, we examined its effects on bone metabolism both in vitro and in vivo. Materials and Methods: We measured the expression of ghrelin and growth hormone secretagogue receptor la (GHS-R1a) in rat osteoblasts using RT-PCR and immunohistochemistry (IHC). The effect of ghrelin on primary osteoblast-like cell proliferation was examined by recording changes in cell number and the level of DNA synthesis. Osteoblast differentiation markers (Runx2, collagen alpha 1 type I [COLI], alkaline phosphatase [ALP], osteocalcin [OCN]) were analyzed using quantitative RT-PCR. We also examined calcium accumulation and ALP activity in osteoblast-like cells induced by ghrelin. Finally, to address the in vivo effects of ghrelin on bone metabolism, we examined the BMD of Sprague-Dawley (SD) rats and genetically GH-deficient, spontaneous dwarf rats (SDR). Results: Ghrelin and GHS-R1a were identified in osteoblast-like cells. Ghrelin significantly increased osteoblast-like cell numbers and DNA synthesis in a dose-dependent manner. The proliferative effects of ghrelin were suppressed by [D-LyS(3)] -GHRP-6, an antagonist of GHS-R1a, in a dose-dependent manner. Furthermore, ghrelin increased the expression of osteoblast differentiation markers, ALP activity, and calcium accumulation in the matrix. Finally, ghrelin definitely increased BMD of both SD rats and SDRs. Conclusions: These observations show that ghrelin directly stimulates bone formation.
引用
收藏
页码:790 / 798
页数:9
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