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HA 释放钙离子对成骨细胞分化的影响。

Effects of HA released calcium ion on osteoblast differentiation.

机构信息

Interdisciplinary Program for Bioengineering, Seoul National University, Seoul, 152-742, Korea.

出版信息

J Mater Sci Mater Med. 2010 May;21(5):1649-54. doi: 10.1007/s10856-010-4011-y. Epub 2010 Feb 17.

Abstract

Hydroxyapatite (HA) is a widely used calcium phosphate implant substitute and has dissolution property. Although HA has been shown a beneficial effect on osteoblast differentiation, the exact mechanism is still unclear. In the present study, we proposed that Ca(2+) released from HA activated the expression bone associated proteins, OPN and BSP, mediated by L-type calcium channel and calcium/calmodulin-dependent protein kinase (CaMK) 2 which resulted into improved osteoblast differentiation. Results showed that HA elevated ALP expression as well as OPN and BSP expression in MC3T3-E1 cells. The result from western blot of CaMK2alpha indicated that HA released Ca(2+) activated CaMK2 through L-type calcium channel. Furthermore, upregulation of OPN and BSP mRNA expression was significantly inhibited when blocking both the L-type calcium channel and CaMK2. These findings suggested that HA accelerated the osteoblast differentiation by releasing Ca(2+).

摘要

羟基磷灰石(HA)是一种广泛应用的磷酸钙植入物替代物,具有溶解性能。尽管 HA 已被证明对成骨细胞分化有有益的影响,但确切的机制仍不清楚。在本研究中,我们提出 HA 释放的 Ca(2+) 通过 L 型钙通道和钙/钙调蛋白依赖性蛋白激酶(CaMK)2 激活骨相关蛋白 OPN 和 BSP 的表达,从而促进成骨细胞分化。结果表明,HA 可提高 MC3T3-E1 细胞中碱性磷酸酶(ALP)的表达以及 OPN 和 BSP 的表达。来自 CaMK2alpha 的 Western blot 结果表明,HA 通过 L 型钙通道释放 Ca(2+) 激活 CaMK2。此外,当同时阻断 L 型钙通道和 CaMK2 时,OPN 和 BSP mRNA 表达的上调显著受到抑制。这些发现表明,HA 通过释放 Ca(2+) 加速成骨细胞分化。

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