Mok Gi Fay, Cardenas Ryan, Anderton Helen, Campbell Keith H S, Sweetman Dylan
Division of Animal Sciences, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Sutton Bonington LE12 5RD, UK.
Division of Animal Sciences, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Sutton Bonington LE12 5RD, UK.
Dev Biol. 2014 Dec 15;396(2):214-23. doi: 10.1016/j.ydbio.2014.10.004. Epub 2014 Oct 18.
During limb development Pax3 positive myoblasts delaminate from the hypaxial dermomyotome of limb level somites and migrate into the limb bud where they form the dorsal and ventral muscle masses. Only then do they begin to differentiate and express markers of myogenic commitment and determination such as Myf5 and MyoD. However the signals regulating this process remain poorly characterised. We show that FGF18, which is expressed in the distal mesenchyme of the limb bud, induces premature expression of both Myf5 and MyoD and that blocking FGF signalling also inhibits endogenous MyoD expression. This expression is mediated by ERK MAP kinase but not PI3K signalling. We also show that retinoic acid (RA) can inhibit the myogenic activity of FGF18 and that blocking RA signalling allows premature induction of MyoD by FGF18 at HH19. We propose a model where interactions between FGF18 in the distal limb and retinoic acid in the proximal limb regulate the timing of myogenic gene expression during limb bud development.
在肢体发育过程中,Pax3阳性成肌细胞从肢体水平体节的轴下生皮节脱离,迁移到肢芽中,在那里形成背侧和腹侧肌肉块。只有到那时它们才开始分化并表达成肌定向和决定的标志物,如Myf5和MyoD。然而,调节这一过程的信号仍不清楚。我们发现,在肢芽远端间充质中表达的FGF18可诱导Myf5和MyoD的过早表达,并且阻断FGF信号也会抑制内源性MyoD的表达。这种表达是由ERK MAP激酶介导的,而不是PI3K信号。我们还发现视黄酸(RA)可以抑制FGF18的成肌活性,并且阻断RA信号会使FGF18在HH19时过早诱导MyoD。我们提出了一个模型,其中肢体远端的FGF18与肢体近端的视黄酸之间的相互作用调节肢芽发育过程中成肌基因表达的时间。