Lavery Danielle L, Martin Jennifer, Turnbull Yvonne D, Hoppler Stefan
Institute of Medical Sciences, Cell and Developmental Biology Research Programme, University of Aberdeen, Foresterhill, Aberdeen, AB25 2ZD, Scotland, UK.
Dev Biol. 2008 Nov 15;323(2):177-88. doi: 10.1016/j.ydbio.2008.08.032. Epub 2008 Sep 9.
Mesodermal tissue with heart forming potential (cardiogenic mesoderm) is induced during gastrulation. This cardiogenic mesoderm later differentiates into heart muscle tissue (myocardium) and non-muscular heart tissue. Inhibition of Wnt/beta-catenin signaling is known to be required early for induction of cardiogenic mesoderm; however, the identity of the inhibiting Wnt signal itself is still elusive. We have identified Wnt6 in Xenopus as an endogenous Wnt signal, which is expressed in tissues close to and later inside the developing heart. Our loss-of-function experiments show that Wnt6 function is required in the embryo to prevent development of an abnormally large heart muscle. We find, however, that Wnt6 is not required as expected during gastrulation stages, but later during organogenesis stages just before cells of the cardiogenic mesoderm begin to differentiate into heart muscle (myocardium). Our gain-of-function experiments show that Wnt6 and also activated canonical Wnt/beta-catenin signaling are capable of restricting heart muscle development at these relatively late stages of development. This repressive role of Wnt signaling is mediated initially via repression of cardiogenic transcription factors, since reinstatement of GATA function can rescue expression of other cardiogenic transcription factors and downstream cardiomyogenic differentiation genes.
具有心脏形成潜能的中胚层组织(生心中胚层)在原肠胚形成过程中被诱导产生。这种生心中胚层随后分化为心肌组织(心肌层)和非肌肉性心脏组织。已知在早期诱导生心中胚层时需要抑制Wnt/β-连环蛋白信号通路;然而,抑制性Wnt信号本身的身份仍然难以捉摸。我们在非洲爪蟾中鉴定出Wnt6作为一种内源性Wnt信号,它在发育中心脏附近及之后的内部组织中表达。我们的功能缺失实验表明,胚胎中需要Wnt6的功能来防止异常大的心肌发育。然而,我们发现,在原肠胚形成阶段并不像预期的那样需要Wnt6,而是在器官发生阶段后期,就在生心中胚层细胞开始分化为心肌(心肌层)之前需要它。我们的功能获得实验表明,Wnt6以及激活的经典Wnt/β-连环蛋白信号通路在这些相对较晚的发育阶段能够限制心肌发育。Wnt信号通路的这种抑制作用最初是通过抑制生心转录因子介导的,因为恢复GATA功能可以挽救其他生心转录因子和下游心肌分化基因的表达。