Pitx2 regulates cardiac left-right asymmetry by patterning second cardiac lineage-derived myocardium

被引:92
作者
Ai, Di
Liu, Wei
Ma, Lijiang
Dong, Feiyan
Lu, Mei-Fang
Wang, Degang
Verzi, Michael P.
Cai, Chenleng
Gage, Philip J.
Evans, Sylvia
Black, Brian L.
Brown, Nigel A.
Martin, James F.
机构
[1] Texas A&M Syst, Hlth Sci Ctr, Inst Biosci & Technol, Houston, TX 77030 USA
[2] Univ Michigan, Dept Ophthalmol & Visual Sci, Ann Arbor, MI 48109 USA
[3] Univ Calif San Diego, Dept Med, Inst Mol Med, La Jolla, CA 92093 USA
[4] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[6] Univ London St Georges Hosp, Sch Med, Div Basic Med Sci, London SW17 0RE, England
关键词
left-right asymmetry; secondary heart field; homeobox;
D O I
10.1016/j.ydbio.2006.06.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Current models of left-right asymmetry hold that an early asymmetric signal is generated at the node and transduced to lateral plate mesoderm in a linear signal transduction cascade through the function of the Nodal signaling molecule. The Pitx2 homeobox gene functions at the final stages of this cascade to direct asymmetric morphogenesis of selected organs including the heart. We previously showed that Pitx2 regulated an asymmetric pathway that was independent of cardiac looping suggesting a second asymmetric cardiac pathway. It has been proposed that in the cardiac outflow tract Pitx2 functions in both cardiac neural crest, as a target of canonical Wnt-signaling, and in the mesoderm-derived cardiac second lineage. We used fate mapping, conditional loss of function, and chimera analysis in mice to investigate the role of Pitx2 in outflow tract morphogenesis. Our findings reveal that Pitx2 is dispensable in the cardiac neural crest but functions in second lineage myocardium revealing that this cardiac progenitor field is patterned asymmetrically. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:437 / 449
页数:13
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