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将心脏Nkx2.5表达域细分为肌源性和非肌源性区室。

Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments.

作者信息

Raffin M, Leong L M, Rones M S, Sparrow D, Mohun T, Mercola M

机构信息

Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA.

出版信息

Dev Biol. 2000 Feb 15;218(2):326-40. doi: 10.1006/dbio.1999.9579.

Abstract

Nkx2.5 is expressed in the cardiogenic mesoderm of avian, mouse, and amphibian embryos. To understand how various cardiac fates within this domain are apportioned, we fate mapped the mesodermal XNkx2.5 domain of neural tube stage Xenopus embryos. The lateral portions of the XNkx2.5 expression domain in the neural tube stage embryo (stage 22) form the dorsal mesocardium and roof of the pericardial cavity while the intervening ventral region closes to form the myocardial tube. XNkx2.5 expression is maintained throughout the period of heart tube morphogenesis and differentiation of myocardial, mesocardial, and pericardial tissues. A series of microsurgical experiments showed that myocardial differentiation in the lateral portion of the field is suppressed during normal development by signals from the prospective myocardium and by tissues located more dorsally in the embryo, in particular the neural tube. These signals combine to block myogenesis downstream of XNkx2.5 and at or above the level of contractile protein gene expression. We propose that the entire XNkx2.5/heart field is transiently specified as cardiomyogenic. Suppression of this program redirects lateral cells to adopt dorsal mesocardial and dorsal pericardial fates and subdivides the field into distinct myogenic and nonmyogenic compartments.

摘要

Nkx2.5在鸟类、小鼠和两栖类胚胎的心脏中胚层中表达。为了了解该区域内各种心脏命运是如何分配的,我们对神经管阶段非洲爪蟾胚胎的中胚层XNkx2.5区域进行了命运图谱分析。神经管阶段胚胎(第22阶段)中XNkx2.5表达区域的外侧部分形成背侧心内膜和心包腔顶部,而中间的腹侧区域闭合形成心肌管。在心脏管形态发生以及心肌、心内膜和心包组织分化的整个过程中,XNkx2.5表达持续存在。一系列显微手术实验表明,在正常发育过程中,该区域外侧部分的心肌分化受到来自预期心肌的信号以及胚胎中更靠背部的组织(特别是神经管)的信号抑制。这些信号共同作用,在XNkx2.5下游以及收缩蛋白基因表达水平或以上阻断肌生成。我们提出,整个XNkx2.5/心脏区域被短暂指定为心肌生成性的。该程序的抑制使外侧细胞转而采用背侧心内膜和背侧心包命运,并将该区域细分为不同的肌生成和非肌生成区室。

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