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牛软骨细胞中胰岛素样生长因子结合蛋白的产生及激素调节

Production and hormonal regulation of insulin-like growth factor binding proteins in bovine chondrocytes.

作者信息

Olney R C, Smith R L, Kee Y, Wilson D M

机构信息

Department of Pediatrics, Stanford University Medical Center, California 94305.

出版信息

Endocrinology. 1993 Aug;133(2):563-70. doi: 10.1210/endo.133.2.7688290.

Abstract

Linear growth results from proliferation and differentiation of chondrocytes within the growth plates and is regulated, in part, by the insulin-like growth factors (IGFs). IGF binding proteins (IGFBPs) also appear to play a significant, but yet unclear, role. To examine IGFBP production by chondrocytes, we isolated bovine chondrocytes from adult articular, fetal articular, and fetal growth plate cartilage, and maintained them in primary culture as high-density monolayers or encapsulated in alginate beads. Cells were cultured in serum-free conditions with human GH (hGH), insulin, hIGF-I, or hIGF-II. Human IGF-I resulted in higher DNA content in all three of the chondrocyte types. Conditioned medium samples were analyzed for IGFBPs by Western ligand blotting. Chondrocytes released IGFBPs of 24, 29, 33, 39, and 43 kilodaltons (kDa). Deglycosylation and immunoblotting identified the 39/43-kDa doublet as IGFBP-3 and the 33-kDa band as IGFBP-2. All chondrocyte types released 29- and 24-kDa IGFBP bands constitutively. Adult articular chondrocytes increased production all IGFBPs in response to IGF-I, but particularly the 29-kDa band (17-fold increase). Fetal articular chondrocytes showed a similar pattern, but with less of an increase when treated with IGF-I. Fetal growth plate chondrocytes primarily showed increases in IGFBP-3 and the 24-kDa form (4.7- and 2.7-fold, respectively) in response to IGF-I. Although the role of IGFBPs in IGF mediation of articular and growth plate chondrocyte metabolism requires further research, we show here that bovine chondrocytes produce IGFBPs, and the IGFs regulate this production.

摘要

线性生长源于生长板内软骨细胞的增殖和分化,部分受胰岛素样生长因子(IGFs)调控。胰岛素样生长因子结合蛋白(IGFBPs)似乎也发挥着重要但尚不清楚的作用。为研究软骨细胞产生IGFBPs的情况,我们从成年关节软骨、胎儿关节软骨和胎儿生长板软骨中分离出牛软骨细胞,并将其作为高密度单层细胞进行原代培养或包封在藻酸盐珠中。细胞在无血清条件下用人生长激素(hGH)、胰岛素、人IGF-I或人IGF-II进行培养。人IGF-I使所有三种类型的软骨细胞中的DNA含量更高。通过Western配体印迹分析条件培养基样品中的IGFBPs。软骨细胞释放出分子量为24、29、33、39和43千道尔顿(kDa)的IGFBPs。去糖基化和免疫印迹鉴定出39/43-kDa双峰为IGFBP-3,33-kDa条带为IGFBP-2。所有类型的软骨细胞都组成性地释放29-kDa和24-kDa的IGFBP条带。成年关节软骨细胞对IGF-I的反应是所有IGFBPs的产生增加,尤其是29-kDa条带(增加了17倍)。胎儿关节软骨细胞表现出类似的模式,但用IGF-I处理时增加幅度较小。胎儿生长板软骨细胞对IGF-I的反应主要表现为IGFBP-3和24-kDa形式增加(分别为4.7倍和2.7倍)。尽管IGFBPs在IGF介导关节和生长板软骨细胞代谢中的作用需要进一步研究,但我们在此表明牛软骨细胞产生IGFBPs,并且IGFs调节这种产生。

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