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骨骼生长因子以及已知存在于骨基质中的其他生长因子可刺激人骨细胞的增殖和蛋白质合成。

Skeletal growth factor and other growth factors known to be present in bone matrix stimulate proliferation and protein synthesis in human bone cells.

作者信息

Wergedal J E, Mohan S, Lundy M, Baylink D J

机构信息

Department of Medicine, Loma Linda University, CA.

出版信息

J Bone Miner Res. 1990 Feb;5(2):179-86. doi: 10.1002/jbmr.5650050212.

Abstract

The purpose of the study was to investigate the effect of skeletal growth factor/insulinlike growth factor II and other growth factors known to be present in bone matrix on the proliferation and differentiation of human bone cells. Cells were isolated by collagenase digestion from femoral heads obtained during hip replacement operations. Cells were cultured in DMEM medium with 10% calf serum. Third to fifth passage cells were plated in multiwell plates and the medium changed to low serum (0.1%) for 2 days. The medium was changed to serum-free medium prior to addition of growth factors. Cell proliferation was measured by the incorporation of [3H]thymidine into DNA and by the percentage of cells that incorporate bromodeoxyuridine. Protein synthesis was measured by the incorporation of [3H]proline into trichloroacetic acid-precipitable material. Skeletal growth factor/insulinlike growth factor II and insulinlike growth factor I stimulated cell proliferation and protein synthesis in a dose-dependent manner. Alkaline phosphatase-specific activity was not increased by these factors. Transforming growth factor beta 1 did not affect cell proliferation but stimulated protein synthesis and increased the specific activity of alkaline phosphatase. Fibroblast growth factor did not affect any of the cell parameters. These studies suggest that skeletal growth factor/insulinlike growth factor II, insulinlike growth factor I, and transforming growth factor beta 1 may play a role in the local control of the proliferation and differentiation of human osteoblasts.

摘要

本研究的目的是调查骨骼生长因子/胰岛素样生长因子II以及已知存在于骨基质中的其他生长因子对人骨细胞增殖和分化的影响。通过胶原酶消化从髋关节置换手术中获取的股骨头分离细胞。细胞在含10%小牛血清的DMEM培养基中培养。将第三代至第五代细胞接种于多孔板中,培养基换成低血清(0.1%)2天。在添加生长因子之前,将培养基换成无血清培养基。通过[3H]胸腺嘧啶核苷掺入DNA以及掺入溴脱氧尿苷的细胞百分比来测量细胞增殖。通过[3H]脯氨酸掺入三氯乙酸可沉淀物质来测量蛋白质合成。骨骼生长因子/胰岛素样生长因子II和胰岛素样生长因子I以剂量依赖方式刺激细胞增殖和蛋白质合成。这些因子未增加碱性磷酸酶的特异性活性。转化生长因子β1不影响细胞增殖,但刺激蛋白质合成并增加碱性磷酸酶的特异性活性。成纤维细胞生长因子不影响任何细胞参数。这些研究表明,骨骼生长因子/胰岛素样生长因子II、胰岛素样生长因子I和转化生长因子β1可能在人成骨细胞增殖和分化的局部调控中发挥作用。

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