Hakim Zeenat S, DiMichele Laura A, Doherty Jason T, Homeister Jonathon W, Beggs Hilary E, Reichardt Louis F, Schwartz Robert J, Brackhan Joseph, Smithies Oliver, Mack Christopher P, Taylor Joan M
Department of Pathology and Carolina Cardiovascular Biology Center, 501 Brinkhous-Bullitt Bldg. CB 7525, University of North Carolina, Chapel Hill, NC 27599, USA.
Mol Cell Biol. 2007 Aug;27(15):5352-64. doi: 10.1128/MCB.00068-07. Epub 2007 May 25.
To examine a role for focal adhesion kinase (FAK) in cardiac morphogenesis, we generated a line of mice with a conditional deletion of FAK in nkx2-5-expressing cells (herein termed FAKnk mice). FAKnk mice died shortly after birth, likely resulting from a profound subaortic ventricular septal defect and associated malalignment of the outflow tract. Additional less penetrant phenotypes included persistent truncus arteriosus and thickened valve leaflets. Thus, conditional inactivation of FAK in nkx2-5-expressing cells leads to the most common congenital heart defect that is also a subset of abnormalities associated with tetralogy of Fallot and the DiGeorge syndrome. No significant differences in proliferation or apoptosis between control and FAKnk hearts were observed. However, decreased myocardialization was observed for the conal ridges of the proximal outflow tract in FAKnk hearts. Interestingly, chemotaxis was significantly attenuated in isolated FAK-null cardiomyocytes in comparison to genetic controls, and these effects were concomitant with reduced tyrosine phosphorylation of Crk-associated substrate (CAS). Thus, it is possible that ventricular septation and appropriate outflow tract alignment is dependent, at least in part, upon FAK-dependent CAS activation and subsequent induction of polarized myocyte movement into the conal ridges. Future studies will be necessary to determine the precise contributions of the additional nkx2-5-derived lineages to the phenotypes observed.
为了研究粘着斑激酶(FAK)在心脏形态发生中的作用,我们构建了一种小鼠品系,其在表达nkx2-5的细胞中条件性缺失FAK(在此称为FAKnk小鼠)。FAKnk小鼠出生后不久即死亡,可能是由于严重的主动脉下室间隔缺损以及相关的流出道排列不齐所致。其他较少见的表型包括永存动脉干和瓣膜小叶增厚。因此,在表达nkx2-5的细胞中条件性失活FAK会导致最常见的先天性心脏缺陷,这也是与法洛四联症和迪乔治综合征相关的异常的一个子集。在对照心脏和FAKnk心脏之间未观察到增殖或凋亡的显著差异。然而,在FAKnk心脏中,观察到近端流出道的圆锥嵴心肌化减少。有趣的是,与基因对照相比,分离的FAK缺失心肌细胞的趋化性显著减弱,并且这些效应与Crk相关底物(CAS)的酪氨酸磷酸化减少同时出现。因此,室间隔形成和适当的流出道排列可能至少部分依赖于FAK依赖的CAS激活以及随后诱导极化的心肌细胞向圆锥嵴移动。未来的研究将有必要确定额外的nkx2-5衍生谱系对所观察到的表型的确切贡献。