Department of Biology, West Virginia University, Morgantown, WV 26506, USA.
Department of Clinical Laboratory, The Affiliated Hospital of KMUST, Medical School, Kunming University of Science and Technology, Kunming 650032, China.
Development. 2018 Apr 4;145(7):dev158154. doi: 10.1242/dev.158154.
During vertebrate gastrulation, canonical Wnt signaling induces the formation of neural plate border (NPB). Wnt is also thought to be required for the subsequent specification of neural crest (NC) lineage at the NPB, but the direct evidence is lacking. We found previously that the disintegrin metalloproteinase ADAM13 is required for Wnt activation and NC induction in Here, we report that knockdown of ADAM13 or its close paralog ADAM19 severely downregulates Wnt activity at the NPB, inhibiting NC specification without affecting earlier NPB formation. Surprisingly, ADAM19 functions nonproteolytically in NC specification by interacting with ADAM13 and inhibiting its proteasomal degradation. Ectopic expression of stabilized ADAM13 mutants that function independently of ADAM19 can induce the NC marker/specifier in the future epidermis via Wnt signaling. These results unveil the essential roles of a novel protease-protease interaction in regulating a distinct wave of Wnt signaling, which directly specifies the NC lineage.
在脊椎动物原肠胚形成过程中,经典 Wnt 信号诱导神经板边界(NPB)的形成。Wnt 也被认为是 NPB 中神经嵴(NC)谱系随后特化所必需的,但直接证据尚缺乏。我们之前发现,解整合素金属蛋白酶 ADAM13 对于 Wnt 的激活和 NC 的诱导是必需的。在这里,我们报告说 ADAM13 或其密切的同源物 ADAM19 的敲低严重下调 NPB 处的 Wnt 活性,抑制 NC 特化而不影响早期 NPB 的形成。令人惊讶的是,ADAM19 通过与 ADAM13 相互作用并抑制其蛋白酶体降解,以非蛋白水解的方式在 NC 特化中发挥作用。稳定表达的 ADAM13 突变体的异位表达可通过 Wnt 信号在未来的表皮中诱导 NC 标记物/决定因子。这些结果揭示了一种新型蛋白酶-蛋白酶相互作用在调节特定 Wnt 信号波中,直接决定 NC 谱系的重要作用。