A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field

Genesis - Tập 45 Số 7 - Trang 470-475 - 2007
Tuong Huynh1,2, Li Chen3,1,2, Phillip Terrell1, Antonio Baldini3,1,4
1Institute of Biosciences and Technology, Texas A&M University Health Sciences Center, Houston, Texas
2Tuong Huynh and Li Chen contributed equally to this work.
3Cardiovascular Sciences Program, Baylor College of Medicine, Houston, Texas
4Telethon Institute of Genetics and Medicine, Naples, Italy

Tóm tắt

Abstract

Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the outflow tract of the heart. Loss of Tbx1 causes heart defects in humans and mice. We report a novel Tbx1Cre knock‐in allele that we use to fate map Tbx1‐expressing cells during development in conjunction with a reporter and 3D image reconstruction. Tbx1 descendants constitute a mesodermal cell population that surrounds the primitive pharynx and approaches the arterial pole of the heart from lateral and posterior, but not anterior directions. These cells populate most of the outflow tract with the exception of the anterior portion, thus identifying a population of the SHF of distinct origin. Both myocardial and underlying endocardial layers were labeled, suggesting a common origin of these cell types. Finally, we show that Tbx1Cre‐positive and Tbx1Cre‐negative cell descendants occupy discrete domains in the outflow tract throughout development. genesis 45:470–475, 2007. Published 2007 Wiley‐Liss, Inc.

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