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骨形态发生蛋白(BMP)和成纤维细胞生长因子(FGF)调控途径控制心脏瓣膜前体细胞的细胞谱系多样化。

BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells.

作者信息

Lincoln Joy, Alfieri Christina M, Yutzey Katherine E

机构信息

Division of Molecular Cardiovascular Biology, MLC 7020, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

Dev Biol. 2006 Apr 15;292(2):292-302. doi: 10.1016/j.ydbio.2005.12.042.

Abstract

The atrioventricular heart valve leaflets and chordae tendineae are composed of diverse cell lineages and highly organized extracellular matrices that share characteristics with cartilage and tendon cell types in the limb buds and somites. During embryonic chicken valvulogenesis, aggrecan and sox9, characteristic of cartilage cells, are observed in the AV valve leaflets, in contrast to tendon-associated genes scleraxis and tenascin, present in the chordae tendineae. In the limb buds and somites, cartilage cell lineage differentiation is regulated by BMP2, while FGF4 controls tendon cell fate. The ability of BMP2 and FGF4 to induce similar patterns of gene expression in heart valve precursor cells was examined. In multiple assays of cells from prefused endocardial cushions, BMP2 is sufficient to activate Smad1/5/8 phosphorylation and induce sox9 and aggrecan expression, while FGF4 treatment increases phosphorylated MAPK (dpERK) signaling and promotes expression of scleraxis and tenascin. However, these treatments do not alter differentiated lineage gene expression in valve progenitors from fused cushions of older embryos. Together, these studies define regulatory pathways of AV valve progenitor cell diversification into leaflets and chordae tendineae that share inductive interactions and differentiation phenotypes with cartilage and tendon cell lineages.

摘要

房室心脏瓣膜小叶和腱索由多种细胞谱系和高度有序的细胞外基质组成,这些细胞外基质与肢芽和体节中的软骨和肌腱细胞类型具有共同特征。在胚胎鸡瓣膜发生过程中,在房室瓣膜小叶中观察到软骨细胞特有的聚集蛋白聚糖和sox9,而腱索中则存在与肌腱相关的基因硬骨素和腱生蛋白。在肢芽和体节中,软骨细胞谱系分化受BMP2调控,而FGF4控制肌腱细胞命运。研究了BMP2和FGF4在心脏瓣膜前体细胞中诱导相似基因表达模式的能力。在对融合前心内膜垫细胞的多次检测中,BMP2足以激活Smad1/5/8磷酸化并诱导sox9和聚集蛋白聚糖表达,而FGF4处理则增加磷酸化MAPK(dpERK)信号传导并促进硬骨素和腱生蛋白的表达。然而,这些处理不会改变来自 older胚胎融合垫的瓣膜祖细胞中分化谱系基因的表达。总之,这些研究确定了房室瓣膜祖细胞分化为小叶和腱索的调控途径,这些途径与软骨和肌腱细胞谱系具有共同的诱导相互作用和分化表型。

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