Aberrant differentiation of second heart field mesoderm prefigures cellular defects in the outflow tract in response to loss of FGF8

被引:3
作者
Astrof, Sophie [1 ]
Arriagada, Cecilia [1 ]
Saijoh, Yukio [2 ]
Francou, Alexandre [3 ]
Kelly, Robert G. [3 ]
Moon, Anne [4 ,5 ,6 ]
机构
[1] Univ Med & Dent New Jersey, Dept Cell Biol & Mol Med, Rutgers Biomed & Hlth Sci, Newark, NJ USA
[2] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT USA
[3] Aix Marseille Univ, Dev Biol Inst Marseille, CNRS UMR 7288, Marseille, France
[4] Geisinger Med Clin, Weis Ctr Res, Dept Mol & Funct Genom, Danville, PA 17821 USA
[5] Univ Utah, Dept Human Genet, Salt Lake City, UT USA
[6] Hess Ctr Sci & Med Mt Sinai, Mindich Child Hlth & Dev Inst, New York, NY USA
关键词
ARTERIAL POLE; MORPHOGENESIS; POLARITY; TBX1; IDENTIFICATION; MYOCARDIUM; LINEAGE; CELLS; PROLIFERATION; ENDODERM;
D O I
10.1016/j.ydbio.2023.04.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development of the outflow tract of the heart requires specification, proliferation and deployment of a progenitor cell population from the second heart field to generate the myocardium at the arterial pole of the heart. Disruption of these processes leads to lethal defects in rotation and septation of the outflow tract. We previously showed that Fibroblast Growth Factor 8 (FGF8) directs a signaling cascade in the second heart field that regulates critical aspects of OFT morphogenesis. Here we show that in addition to the survival and proliferation cues previously described, FGF8 provides instructive and patterning information to OFT myocardial cells and their progenitors that prevents their aberrant differentiation along a working myocardial program.
引用
收藏
页码:10 / 21
页数:12
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