Retinoic acid signaling is essential for formation of the heart tube in Xenopus

• Published in: Developmental biology Vol. 291; no. 1; pp. 96 - 109
• Main Authors: Collop, Andrew H., Broomfield, Joel A.S., Chandraratna, Roshantha A.S., Yong, Zhao, Deimling, Steven J., Kolker, Sandra J., Weeks, Daniel L., Drysdale, Thomas A.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2006
• Subjects: Animals; Body Patterning; Cardiac troponin I; Cardiogenesis; Embryo, Nonmammalian - metabolism; Female; GATA-4; GATA4 Transcription Factor - biosynthesis; GATA4 Transcription Factor - physiology; Gene Expression Regulation, Developmental; Heart - embryology; Heart development; Homeobox Protein Nkx-2.5; Homeodomain Proteins - biosynthesis; Homeodomain Proteins - physiology; Left–right asymmetry; Mesoderm - physiology; Myocardium - metabolism; Nkx2.5; Retinoic acid; Retinoic acid antagonist; Signal Transduction; Transcription Factors - biosynthesis; Transcription Factors - physiology; Tretinoin - antagonists & inhibitors; Tretinoin - physiology; Xenopus; Xenopus laevis; Xenopus Proteins - biosynthesis; Xenopus Proteins - physiology; Xenopus; Cardiac troponin I; Retinoic acid antagonist; Heart development; Nkx2.5; Cardiogenesis; Retinoic acid; GATA-4; Left–right asymmetry
• DOI: 10.1016/j.ydbio.2005.12.018
• ISSN: 0012-1606

Retinoic acid is clearly important for the development of the heart. In this paper, we provide evidence that retinoic acid is essential for multiple aspects of cardiogenesis in Xenopus by examining embryos that have been exposed to retinoic acid receptor antagonists. Early in cardiogenesis, retinoic acid alters the expression of key genes in the lateral plate mesoderm including Nkx2.5 and HAND1, indicating that early patterning of the lateral plate mesoderm is, in part, controlled by retinoic acid. We found that, in Xenopus, the transition of the heart from a sheet of cells to a tube required retinoic acid signaling. The requirement for retinoic acid signaling was determined to take place during a narrow window of time between embryonic stages 14 and 18, well before heart tube closure. At the highest doses used, the lateral fields of myocardium fail to fuse, intermediate doses lead to a fusion of the two sides but failure to form a tube, and embryos exposed to lower concentrations of antagonist form a heart tube that failed to complete all the landmark changes that characterize looping. The myocardial phenotypes observed when exposed to the retinoic acid antagonist resemble the myocardium from earlier stages of cardiogenesis, although precocious expression of cardiac differentiation markers was not seen. The morphology of individual cells within the myocardium appeared immature, closely resembling the shape and size of cells at earlier stages of development. However, the failures in morphogenesis are not merely a slowing of development because, even when allowed to develop through stage 40, the heart tubes did not close when embryos were exposed to high levels of antagonist. Indeed, some aspects of left–right asymmetry also remained even in hearts that never formed a tube. These results demonstrate that components of the retinoic acid signaling pathway are necessary for the progression of cardiac morphogenesis in Xenopus.