首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Retinoic acid controls heart anteroposterior patterning by down-regulating Isl1 through the Fgf8 pathway.
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Retinoic acid controls heart anteroposterior patterning by down-regulating Isl1 through the Fgf8 pathway.

机译:维甲酸可通过Fgf8途径下调Isl1,从而控制心脏的前后模式。

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摘要

Distinct progenitor cell populations exist in cardiac mesoderm important for patterning of the heart. During heart tube formation in mouse, Tbx5 is expressed in progenitors located more laterally, whereas Isl1 and Fgf8 are expressed in progenitors located more medially. Signals that drive mesodermal progenitors into various cardiac lineages include Fgf8, which functions to induce Isl1. Studies in chick and zebrafish have shown that retinoic acid restricts the number of cardiac progenitors, but its role in mammalian cardiac development is unclear. Here, we demonstrate that Raldh2(-/-) mouse embryos lacking retinoic acid signaling exhibit a posterior expansion of the cardiac Fgf8 expression domain as well as an expansion of Isl1 expression into mesoderm lying posterior to the cardiac field. We provide evidence that retinoic acid acts specifically in the posterior-medial region of the cardiac field to establish the heart posterior boundary potentially by reducing Fgf8 expression which restricts the Isl1 domain.
机译:心脏中胚层中存在不同的祖细胞群,这对心脏的形成至关重要。在小鼠的心管形成过程中,Tbx5在位于更外侧的祖细胞中表达,而Isl1和Fgf8在位于更内侧的祖细胞中表达。驱动中胚层祖细胞进入各种心脏谱系的信号包括Fgf8,其功能是诱导Isl1。在小鸡和斑马鱼中的研究表明,视黄酸会限制心脏祖细胞的数量,但其在哺乳动物心脏发育中的作用尚不清楚。在这里,我们证明缺少视黄酸信号的Raldh2(-/-)小鼠胚胎显示出心脏Fgf8表达域的后向扩展以及Isl1表达向位于心脏后方的中胚层的扩展。我们提供的证据表明,视黄酸可能通过减少限制Isl1结构域的Fgf8表达而在心脏区域的后内侧区域中发挥特定作用,从而建立心脏的后边界。

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