Abstract

Vertebrate limbs originate from the lateral plate mesoderm (LPM) and the overlying ectoderm. While normal limb formation in defined regions has been well studied, the question of whether other positions retain limb-forming potential has not been fully investigated in mice. By ectopically activating β-catenin in the ectoderm with Msx2-cre, we observed that local tissue outgrowths were induced, which either progressed into limb-like structure within the inter-limb flank or formed extra tissues in other parts of the mouse embryo. In the presumptive abdominal region of severely affected embryos, ectopic limb formation was coupled with impaired abdominal ventral body wall (AVBW) closure, which indicates the existence of a potential counterbalance of limb formation and AVBW closure. At the molecular level, constitutive β-catenin activation was sufficient to trigger, but insufficient to maintain the ectopic expression of a putative limb-inducing factor, Fgf8, in the ectoderm. These findings provide new insight into the mechanism of limb formation and AVBW closure, and the crosstalk between the Wnt/β-catenin pathway and Fgf signal.

Highlights

  • In vertebrates, the lateral plate mesoderm (LPM) is located in the flank of the embryonic trunk and gives rise to the mesoderm of multiple organs and tissues, which includes limbs and the abdominal ventral body wall (AVBW).Specification of the prospective limb territories in LPM requires the participation of the homeobox and Tbx genes [1,2,3,4]

  • The LPM cells undergo continuous proliferation and bulge outwards, and express Fgf10, inducing the overlying ectoderm to thicken in the most distal region, forming a structure known as the apical ectodermal ridge (AER), in turn producing Fgf8 to maintain the expression of Fgf10 in the underlying LPM [5]

  • We subsequently investigated whether disrupted limb formation promoted AVBW closure

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Summary

Introduction

Specification of the prospective limb territories in LPM requires the participation of the homeobox and Tbx genes [1,2,3,4]. In addition to the Fgf gene family, Wnt proteins are involved in the limb initiation. Wnt2b and Wnt8c are expressed in the LPM of the presumptive forelimb and hindlimb regions, respectively, where they could both directly induce the expression of Fgf10 [8]. Another Wnt protein, Wnt3a, acts downstream of Fgf to activate and maintain the expression of

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