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甲状旁腺激素-Smad3轴发挥抗凋亡作用,并增强成骨细胞中转化生长因子β的合成代谢作用。

Parathyroid hormone-Smad3 axis exerts anti-apoptotic action and augments anabolic action of transforming growth factor beta in osteoblasts.

作者信息

Sowa Hideaki, Kaji Hiroshi, Iu Mei Fway, Tsukamoto Tatsuo, Sugimoto Toshitsugu, Chihara Kazuo

机构信息

Division of Endocrinology/Metabolism, Neurology and Hematology/Oncology, Department of Clinical Molecular Medicine, Kobe University Graduate School of Medicine, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.

出版信息

J Biol Chem. 2003 Dec 26;278(52):52240-52. doi: 10.1074/jbc.M302566200. Epub 2003 Sep 29.

Abstract

Although several studies indicated that parathyroid hormone (PTH) exerted anabolic action on bone, its precise mechanisms have been unknown. On the other hand, transforming growth factor beta (TGF-beta), abundantly stored in bone matrix, stimulates bone formation with a local injection in rodents. Although our previous study suggested that Smad3 is an important molecule for the stimulation of bone formation, no reports have been available about the effects of PTH on Smad3. In this present study, we examined the effects of PTH on Smad3 and the physiological significance in mouse osteoblastic cells. PTH promoted the expression of Smad3 mRNA within 10 min and the protein level in a dose-dependent manner in MC3T3-E1 and rat osteoblastic UMR-106 cells. Protein kinase A (PKA) activator as well as protein kinase C (PKC) activators increased Smad3 protein level, and both PKA and PKC inhibitors antagonized PTH-induced Smad3, indicating that PTH promotes the production of Smad3 through both PKA and PKC pathways. Next, we examined anti-apoptotic effects of PTH and Smad3 in these cells, employing trypan blue, transferase-mediated nick end labeling, and Hoechst staining. Pretreatment with PTH or overexpression of Smad3 decreased the number of apoptotic cells induced by dexamethasone and etoposide. Moreover, a dominant negative mutant, Smad3DeltaC, abrogated PTH-induced anti-apoptotic effects. On the other hand, PTH augmented TGF-beta-induced transcriptional activity. Furthermore, PTH enhanced TGF-beta-induced production of type I collagen, whereas it did not affect TGF-beta-reduced proliferation in MC3T3-E1 cells. These observations indicated that PTH amplified the anabolic effects of TGF-beta by accelerating the transcriptional activity of Smad3. In conclusion, we first demonstrated that PTH-Smad3 axis exerts anti-apoptotic effects in osteoblasts and reinforces the anabolic action by TGF-beta in osteoblasts. Hence, PTH-Smad3 axis might be involved in the bone anabolic action of PTH.

摘要

尽管多项研究表明甲状旁腺激素(PTH)对骨骼具有合成代谢作用,但其确切机制尚不清楚。另一方面,大量储存在骨基质中的转化生长因子β(TGF-β),通过在啮齿动物体内局部注射可刺激骨形成。虽然我们之前的研究表明Smad3是刺激骨形成的重要分子,但尚无关于PTH对Smad3影响的报道。在本研究中,我们检测了PTH对Smad3的影响及其在小鼠成骨细胞中的生理意义。PTH在10分钟内以剂量依赖性方式促进MC3T3-E1和大鼠成骨UMR-106细胞中Smad3 mRNA的表达和蛋白水平。蛋白激酶A(PKA)激活剂以及蛋白激酶C(PKC)激活剂均可增加Smad3蛋白水平,且PKA和PKC抑制剂均拮抗PTH诱导的Smad3,这表明PTH通过PKA和PKC途径促进Smad3的产生。接下来,我们采用台盼蓝、转移酶介导的缺口末端标记和Hoechst染色,检测了PTH和Smad3在这些细胞中的抗凋亡作用。用PTH预处理或过表达Smad3可减少地塞米松和依托泊苷诱导的凋亡细胞数量。此外,显性负突变体Smad3DeltaC消除了PTH诱导的抗凋亡作用。另一方面,PTH增强了TGF-β诱导的转录活性。此外,PTH增强了TGF-β诱导的I型胶原产生,而它不影响TGF-β降低的MC3T3-E1细胞增殖。这些观察结果表明,PTH通过加速Smad3的转录活性增强了TGF-β的合成代谢作用。总之,我们首次证明PTH-Smad3轴在成骨细胞中发挥抗凋亡作用,并增强TGF-β在成骨细胞中的合成代谢作用。因此,PTH-Smad3轴可能参与了PTH的骨合成代谢作用。

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