首页> 外文期刊>European Journal of Pharmacology: An International Journal >A novel member of the calcitonin gene-related peptide family, calcitonin receptor-stimulating peptide, inhibits the formation and activity of osteoclasts.
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A novel member of the calcitonin gene-related peptide family, calcitonin receptor-stimulating peptide, inhibits the formation and activity of osteoclasts.

机译:降钙素基因相关肽家族的一个新成员,降钙素受体刺激肽,抑制破骨细胞的形成和活性。

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摘要

We isolated a novel peptide, calcitonin receptor-stimulating peptide-1 (CRSP-1), from porcine brain and found that the administration of this peptide into rats induced a transient decrease in plasma calcium concentration. Therefore, we investigated the effects of CRSP-1 on osteoclastogenesis. Osteoclast-like cells were formed from spleen cells or bone marrow cells by a combination of the receptor activator of nuclear factor-kappaB ligand (RANKL) and macrophage colony-stimulating factor (M-CSF). CRSP-1 dose-dependently inhibited the formation of multinucleated osteoclast-like cells, and a calcitonin receptor inhibitor antagonized in part the inhibition of osteoclast formation by CRSP-1. Furthermore, CRSP-1 destroyed the actin ring that is a typical index of osteoclast resorption activity; it contributed to this action via the signaling pathway of protein kinase A. Our findings indicate that CRSP-1 inhibits osteoclastogenesis by inhibiting the formation and activity of multinucleated osteoclasts. The inhibitory effects of CRSP-1 on osteoclast metabolism were similar in degree to those of porcine calcitonin. CRSP-1 might provide a clue to the development of tools useful in the prevention and treatment of osteoporosis.
机译:我们从猪脑中分离出一种新型肽,降钙素受体刺激肽1(CRSP-1),发现将这种肽施用于大鼠会引起血浆钙浓度的短暂降低。因此,我们研究了CRSP-1对破骨细胞形成的影响。破骨细胞样细胞是由脾细胞或骨髓细胞通过核因子-κB配体(RANKL)受体激活剂和巨噬细胞集落刺激因子(M-CSF)的组合而形成的。 CRSP-1剂量依赖性地抑制了多核破骨细胞样细胞的形成,而降钙素受体抑制剂部分拮抗了CRSP-1对破骨细胞形成的抑制作用。此外,CRSP-1破坏了肌动蛋白环,这是破骨细胞吸收活性的典型指标。我们的发现表明CRSP-1通过抑制多核破骨细胞的形成和活性来抑制破骨细胞的生成。 CRSP-1对破骨细胞代谢的抑制作用在程度上与猪降钙素相似。 CRSP-1可能为开发用于预防和治疗骨质疏松症的工具提供了线索。

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