Affiliation:
1. Departments of Zoology and Anatomy and Neuroscience Training Program,University of Wisconsin, Madison, WI 53706, USA.
Abstract
Neural crest cells (NCCs) are pluripotent migratory cells that are crucial to the development of the peripheral nervous system, pigment cells and craniofacial cartilage and bone. NCCs are specified within the dorsal ectoderm and undergo an epithelial to mesenchymal transition (EMT) in order to migrate to target destinations where they differentiate. Here we report a role for a member of the semaphorin family of cell guidance molecules in NCC development. Morpholino-mediated knockdown of Sema3d inhibits the proliferation of hindbrain neuroepithelial cells. In addition, Sema3d knockdown reduces markers of migratory NCCs and disrupts NCC-derived tissues. Similarly, expression of a dominant-repressor form of TCF (ΔTCF) reduces hindbrain cell proliferation and leads to a disruption of migratory NCC markers. Moreover,expression of ΔTCF downregulates sema3d RNA expression. Finally, Sema3d overexpression rescues reduced proliferation caused byΔTCF expression, suggesting that Sema3d lies downstream of Wnt/TCF signaling in the molecular pathway thought to control cell cycle in NCC precursors.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Cited by
36 articles.
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