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胚胎肢体间充质微团培养软骨形成过程中的Sox9表达。

Sox9 expression during chondrogenesis in micromass cultures of embryonic limb mesenchyme.

作者信息

Kulyk W M, Franklin J L, Hoffman L M

机构信息

Department of Anatomy, University of Saskatchewan, Saskatoon, Saskatchewan, S7N 5E5, Canada.

出版信息

Exp Cell Res. 2000 Mar 15;255(2):327-32. doi: 10.1006/excr.1999.4784.

Abstract

Sox9 plays a crucial role in chondrogenesis. It encodes an HMG-domain transcription factor that activates an enhancer in the gene for type II collagen (Col2a1), a principal cartilage matrix protein. We have characterized the temporal pattern of Sox9 RNA expression in micromass culture, a widely used in vitro model for the analysis of embryonic cartilage differentiation. Cultures were prepared from distal subridge mesenchyme of the stage 24/25 chick embryo wing bud, which undergoes uniform chondrogenic differentiation in vitro. The early "prechondrogenic" phase of culture was characterized by the activation of Sox9 RNA expression, which preceded detectable upregulation of Col2a1 transcription. Sox9 RNA levels peaked between 20 and 65 h of culture, a phase of progressive Col2a1 transcript accumulation, then declined in the mature cartilage of 120-h cultures. Staurosporine treatment enhanced chondrogenesis in micromass culture by inducing a rapid quantitative increase in Sox9 transcript levels. However, PMA, a phorbol ester that inhibits Col2a1 expression and chondrocyte differentiation, had an unexpectedly modest effect on Sox9 RNA accumulation.

摘要

Sox9在软骨形成过程中发挥着关键作用。它编码一种HMG结构域转录因子,该因子可激活II型胶原蛋白(Col2a1)基因中的一个增强子,Col2a1是一种主要的软骨基质蛋白。我们已经在微团培养中确定了Sox9 RNA表达的时间模式,微团培养是一种广泛用于分析胚胎软骨分化的体外模型。培养物取自24/25期鸡胚翼芽的远端嵴下间充质,其在体外经历均匀的软骨形成分化。培养的早期“软骨形成前期”阶段的特征是Sox9 RNA表达的激活,这先于Col2a1转录的可检测上调。Sox9 RNA水平在培养20至65小时之间达到峰值,这是Col2a1转录本逐渐积累的阶段,然后在120小时培养的成熟软骨中下降。星形孢菌素处理通过诱导Sox9转录本水平的快速定量增加来增强微团培养中的软骨形成。然而,佛波酯PMA可抑制Col2a1表达和软骨细胞分化,但其对Sox9 RNA积累的影响出人意料地较小。

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