Division of Biology and Biological Engineering, California Institute of Technology, 1200 E California Boulevard, Pasadena, CA 91125, USA.
Division of Biology and Biological Engineering, California Institute of Technology, 1200 E California Boulevard, Pasadena, CA 91125, USA
Development. 2018 Oct 24;145(20):dev164046. doi: 10.1242/dev.164046.
Neural crest cells migrate long distances throughout the embryo and rely on extracellular signals that attract, repel and/or stimulate survival to ensure proper contribution to target derivatives. Here, we show that leukocyte receptor tyrosine kinase (LTK), an ALK-type receptor tyrosine kinase, is expressed by neural crest cells during early migratory stages in chicken embryos. Loss of LTK in the cranial neural crest impairs migration and results in increased levels of apoptosis. Conversely, midkine, previously proposed as a ligand for ALK, is secreted by the non-neural ectoderm during early neural crest migratory stages and internalized by neural crest cells Similar to loss of LTK, loss of midkine reduces survival of the migratory neural crest. Moreover, we show by proximity ligation and co-immunoprecipitation assays that midkine binds to LTK. Taken together, these results suggest that LTK in neural crest cells interacts with midkine emanating from the non-neural ectoderm to promote cell survival, revealing a new signaling pathway that is essential for neural crest development.
神经嵴细胞在胚胎中长距离迁移,并依赖于吸引、排斥和/或刺激存活的细胞外信号,以确保对靶衍生物的适当贡献。在这里,我们表明白细胞受体酪氨酸激酶(LTK),一种 ALK 型受体酪氨酸激酶,在鸡胚胎的早期迁移阶段由神经嵴细胞表达。颅神经嵴中的 LTK 缺失会损害迁移并导致细胞凋亡水平增加。相反,中期因子(midkine),以前被提议为 ALK 的配体,在早期神经嵴迁移阶段由非神经外胚层分泌,并被神经嵴细胞内化。与 LTK 缺失相似,中期因子缺失会降低迁移的神经嵴细胞的存活率。此外,我们通过接近连接和共免疫沉淀测定表明,中期因子与来自非神经外胚层的 LTK 结合。综上所述,这些结果表明神经嵴细胞中的 LTK 与从中胚层分泌的中期因子相互作用,以促进细胞存活,揭示了一条对神经嵴发育至关重要的新信号通路。