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使用原代软骨细胞的微团培养分析软骨成熟情况。

Analysis of cartilage maturation using micromass cultures of primary chondrocytes.

作者信息

Kameda T, Koike C, Saitoh K, Kuroiwa A, Iba H

机构信息

Department of Gene Regulation, Institute of Medical Science, University of Tokyo, Japan.

出版信息

Dev Growth Differ. 2000 Jun;42(3):229-36. doi: 10.1046/j.1440-169x.2000.00508.x.

Abstract

A micromass culture (MM-C) system of primary immature chondrocytes for functional analysis of soluble factors involved in the maturation step of cartilage was previously developed. Ectopically expressed BMP-2 was shown to induce the expression of the Ihh and Noggin genes. Here it is demonstrated that, upon longer culture, secreted bone morphogenetic protein-2 (BMP-2) further promotes the maturation step as judged by the induction of type X collagen and BMP-6 expression, which are known to be detectable in the later phase of cartilage maturation. Induction of all of these genes by secreted BMP-2 was not inhibited by ectopic expression of parathyroid hormone-related peptide (PTHrP) induced by retrovirus vector infection, although the same virus vector showed strong inhibitory effects on the expression of type X collagen gene or alkaline phosphatase activity in mature chondrocytes. These results suggest that the maturation-promoting activity exhibited by BMP-2 is dominant over the suppressive effect of PTHrP in immature chondrocytes. When the BMP-6 gene was introduced into the same virus vector as that used for BMP-2, it induced the same sets of genes (Ihh, Noggin, type X collagen and endogenous BMP-6) as BMP-2 did. These results also suggest that BMP-6 would autonomously maintain and/or promote a later stage of chondrocytic maturation.

摘要

我们之前开发了一种用于软骨成熟步骤中可溶性因子功能分析的原代未成熟软骨细胞微团培养(MM-C)系统。异位表达的骨形态发生蛋白-2(BMP-2)可诱导印度刺猬(Ihh)基因和头蛋白(Noggin)基因的表达。在此证明,在更长时间的培养后,分泌的骨形态发生蛋白-2(BMP-2)通过诱导X型胶原和BMP-6的表达进一步促进成熟步骤,已知这些在软骨成熟后期是可检测到的。分泌的BMP-2对所有这些基因的诱导不受逆转录病毒载体感染诱导的甲状旁腺激素相关肽(PTHrP)异位表达的抑制,尽管相同的病毒载体对成熟软骨细胞中X型胶原基因的表达或碱性磷酸酶活性具有强烈的抑制作用。这些结果表明,BMP-2表现出的促进成熟活性在未成熟软骨细胞中比PTHrP的抑制作用占主导地位。当将BMP-6基因导入与用于BMP-2相同的病毒载体时,它诱导与BMP-2相同的一组基因(Ihh、Noggin、X型胶原和内源性BMP-6)。这些结果还表明,BMP-6将自主维持和/或促进软骨细胞成熟的后期阶段。

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