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骨形态发生蛋白 2、5 和 6 联合体外刺激成骨细胞但不刺激破骨细胞。

Bone morphogenetic proteins 2, 5, and 6 in combination stimulate osteoblasts but not osteoclasts in vitro.

机构信息

University Hospital of Cranio, Maxillofacial and Oral Surgery, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.

出版信息

J Orthop Res. 2010 Nov;28(11):1431-9. doi: 10.1002/jor.21144.

Abstract

Bone regeneration is required for fracture healing. Various procedures have been used to promote osteogenesis with bone morphogenetic proteins (BMPs). We assessed the effects of BMP-2, BMP-5, and BMP-6 in isolated and combined use on the generation of osteoblasts and osteoclasts by comparing the osteoclastic potency of each on osteoclasts of primary murine bone marrow cells. Subsequently, cells were stained for tartrate-resistant acid phosphatase, and real time PCR analysis of receptor activator of NKκB ligand and osteoprotegerin was conducted. The same combination of BMPs was used to assess their potential to enhance osteoblasts, employing a mineralization assay and real-time PCR analysis of collagen type-1, runx2, and osterix. While BMP-2 alone and the combination of BMP-2 and BMP-5 significantly enhanced osteoclastogenesis, BMP-2, BMP-5, and BMP-6 in combination did not have additional effects. However, the combined use of BMP-2, BMP-5, and BMP-6 had an additive effect on matrix mineralization and osterix expression in osteoblasts. Our study shows that the combination of BMP-2, BMP-5, and BMP-6 stimulates osteoblasts but not osteoclastogenesis. Thus, the synergistic use of various BMPs might improve effective bone regeneration in the clinical setting.

摘要

骨再生是骨折愈合所必需的。已经使用了各种方法来促进成骨作用,使用骨形态发生蛋白(BMPs)。我们通过比较每种蛋白对原代鼠骨髓细胞破骨细胞的破骨潜能,评估了 BMP-2、BMP-5 和 BMP-6 单独和联合使用对成骨细胞和破骨细胞生成的影响。随后,对细胞进行抗酒石酸酸性磷酸酶染色,并对核因子-κB 受体激活剂配体和骨保护素进行实时 PCR 分析。使用相同的 BMP 组合来评估它们增强成骨细胞的潜力,采用矿化测定和实时 PCR 分析胶原类型-1、runx2 和osterix。虽然 BMP-2 单独使用和 BMP-2 与 BMP-5 的联合使用显著增强了破骨细胞生成,但 BMP-2、BMP-5 和 BMP-6 的联合使用没有额外的效果。然而,BMP-2、BMP-5 和 BMP-6 的联合使用对成骨细胞的基质矿化和osterix 表达有相加作用。我们的研究表明,BMP-2、BMP-5 和 BMP-6 的联合使用刺激成骨细胞,但不刺激破骨细胞生成。因此,联合使用各种 BMP 可能会改善临床环境中的有效骨再生。

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