Department of Surgery, Weill Cornell Medical College, Cornell University, 1300 York Ave., LC-708, New York, NY, USA.
Development. 2013 Sep;140(18):3787-98. doi: 10.1242/dev.093567. Epub 2013 Jul 31.
Biphasic control of WNT signaling is essential during cardiogenesis, but how the pathway switches from promoting cardiac mesoderm to restricting cardiomyocyte progenitor fate is unknown. We identified genes expressed in lateral mesoderm that are dysregulated in zebrafish when both gata5 and gata6 are depleted, causing a block to cardiomyocyte specification. This screen identified tmem88a, which is expressed in the early cardiac progenitor field and was previously implicated in WNT modulation by overexpression studies. Depletion of tmem88a results in a profound cardiomyopathy, secondary to impaired cardiomyocyte specification. In tmem88a morphants, activation of the WNT pathway exacerbates the cardiomyocyte deficiency, whereas WNT inhibition rescues progenitor cells and cardiogenesis. We conclude that specification of cardiac fate downstream of gata5/6 involves activation of the tmem88a gene to constrain WNT signaling and expand the number of cardiac progenitors. Tmem88a is a novel component of the regulatory mechanism controlling the second phase of biphasic WNT activity essential for embryonic cardiogenesis.
WNT 信号的双相调控对于心脏发生至关重要,但该途径如何从促进心脏中胚层转变为限制心肌细胞祖细胞命运尚不清楚。我们鉴定了在 gata5 和 gata6 耗尽的斑马鱼中表达异常的侧中胚层基因,导致心肌细胞特化受阻。该筛选鉴定了 tmem88a,它在早期心肌祖细胞区室中表达,并在过表达研究中被先前牵连到 WNT 调节。tmem88a 的耗竭导致严重的心肌病,继发于心肌细胞特化受损。在 tmem88a 形态发生体中,WNT 途径的激活加剧了心肌细胞的缺乏,而 WNT 抑制则挽救了祖细胞和心脏发生。我们得出结论,gata5/6 下游的心脏命运特化涉及 tmem88a 基因的激活,以限制 WNT 信号并增加心肌祖细胞的数量。Tmem88a 是控制双相 WNT 活性第二阶段的调节机制的一个新组成部分,对于胚胎心脏发生至关重要。