Waxman Joshua S, Keegan Brian R, Roberts Richard W, Poss Kenneth D, Yelon Deborah
Department of Cell Biology, Kimmel Center for Biology and Medicine, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Dev Cell. 2008 Dec;15(6):923-34. doi: 10.1016/j.devcel.2008.09.009.
How adjacent organ fields communicate during development is not understood. Here, we identify a mechanism in which signaling within the forelimb field restricts the potential of the neighboring heart field. In zebrafish embryos deficient in retinoic acid (RA) signaling, the pectoral fins (forelimbs) are lost while both chambers of the heart are enlarged. We provide evidence that both of these phenotypes are due to RA signaling acting directly within the forelimb field. hoxb5b, an RA-responsive gene expressed within the forelimb field, is required to restrict the number of atrial cells arising from the adjacent heart field, although its function is dispensable for forelimb formation. Together, these data indicate nonautonomous influences downstream of RA signaling that act to limit individual chamber size. Therefore, our results offer new perspectives on the mechanisms regulating organ size and the possible causes of congenital syndromes affecting both the heart and forelimb.
在发育过程中相邻器官区域如何相互作用尚不清楚。在此,我们确定了一种机制,即前肢区域内的信号传导限制了相邻心脏区域的潜能。在视黄酸(RA)信号传导缺陷的斑马鱼胚胎中,胸鳍(前肢)缺失,而心脏的两个腔室都增大。我们提供的证据表明,这两种表型都是由于RA信号直接在前肢区域起作用。hoxb5b是在前肢区域表达的一种RA反应基因,它是限制来自相邻心脏区域的心房细胞数量所必需的,尽管其功能对于前肢形成是可有可无的。这些数据共同表明,RA信号下游存在非自主影响,其作用是限制各个腔室的大小。因此,我们的结果为调节器官大小的机制以及影响心脏和前肢的先天性综合征的可能病因提供了新的视角。