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指骨形成区域独特的SMAD1/5/8活性决定了手指身份。

Unique SMAD1/5/8 activity at the phalanx-forming region determines digit identity.

作者信息

Suzuki Takayuki, Hasso Sean M, Fallon John F

机构信息

Department of Anatomy University of Wisconsin, 1300 University Avenue, Madison, WI 53706, USA.

出版信息

Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4185-90. doi: 10.1073/pnas.0707899105. Epub 2008 Mar 11.

Abstract

The zone of polarizing activity is the primary signaling center controlling anterior-posterior patterning of the amniote limb bud. The autopodial interdigits (IDs) are secondary signaling centers proposed to determine digit identity by acting on the cells of the digital ray. Here, we focus on events accompanying digital fate determination and define a region of the digital ray that expresses Sox9 and Bmpr1b and is phosphorylated-SMAD1/5/8 (p-SMAD1/5/8) positive. We name this region the phalanx-forming region (PFR), and show that the PFR cells arise from the distal subridge mesenchyme of digital ray. This phalanx-forming cell lineage is subsequently committed to the cartilage lineage; the fate of these cells is initially labile but becomes fixed as they are incorporated into the condensed cartilage of the digit primordium. Using an in vivo reporter assay, we establish that each digital PFR has a unique p-SMAD1/5/8 activity signature. In addition, we show that changes in this activity correlate with the identity of the digit that forms after experimental manipulation, supporting the idea that threshold signaling levels can lead to different developmental outcomes in a morphogenetic field. Our data define the molecular profile of the PFR, and we propose a model for understanding formation and variation of digits during autopodial development.

摘要

极化活性区是控制羊膜动物肢体芽前后模式形成的主要信号中心。 autopodial 指间组织(IDs)是次级信号中心,被认为通过作用于指射线的细胞来确定指的身份。在这里,我们关注伴随指命运决定的事件,并定义了指射线中一个表达Sox9和Bmpr1b且磷酸化SMAD1/5/8(p-SMAD1/5/8)呈阳性的区域。我们将这个区域命名为指骨形成区(PFR),并表明PFR细胞起源于指射线的远侧子嵴间充质。这个指骨形成细胞谱系随后定向分化为软骨谱系;这些细胞的命运最初是不稳定的,但随着它们被纳入指原基的凝聚软骨中而变得固定。使用体内报告基因检测,我们确定每个指的PFR都有独特的p-SMAD1/5/8活性特征。此外,我们表明这种活性的变化与实验操作后形成的指的身份相关,支持了阈值信号水平可导致形态发生场中不同发育结果的观点。我们的数据定义了PFR的分子特征,并且我们提出了一个模型来理解autopodial发育过程中手指的形成和变异。

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