| Literature DB >> 25224220 |
Qinghang Meng1, Maureen Mongan1, Jingjing Wang1, Xiaofang Tang2, Jinling Zhang1, Winston Kao3, Ying Xia1,3.
Abstract
Epithelial sheet movement is an essential morphogenetic process during mouse embryonic eyelid closure in which Mitogen-Activated Protein 3 Kinase 1 (MAP3K1) and c-Jun play a critical role. Here we show that MAP3K1 associates with the cytoskeleton, activates Jun N-terminal kinase (JNK) and actin polymerization, and promotes the eyelid inferior epithelial cell elongation and epithelium protrusion. Following epithelium protrusion, c-Jun begins to express and acts to promote ERK phosphorylation and migration of the protruding epithelial cells. Homozygous deletion of either gene causes defective eyelid closure, but non-allelic non-complementation does not occur between Map3k1 and c-Jun and the double heterozygotes have normal eyelid closure. Results from this study suggest that MAP3K1 and c-Jun signal through distinct temporal-spatial pathways and that productive epithelium movement for eyelid closure requires the consecutive action of MAP3K1-dependent cytoskeleton reorganization followed by c-Jun-mediated migration.Entities:
Keywords: Embryonic eyelid closure; MAP3K1; c-Jun
Mesh:
Substances:
Year: 2014 PMID: 25224220 PMCID: PMC4204485 DOI: 10.1016/j.ydbio.2014.09.001
Source DB: PubMed Journal: Dev Biol ISSN: 0012-1606 Impact factor: 3.582