Mirror-symmetric microtubule assembly and cell interactions drive lumen formation in the zebrafish neural rod

被引:54
作者
Buckley, Clare E. [1 ]
Ren, Xiaoyun [1 ]
Araya, Claudio [1 ]
Green, Mary J. [1 ]
Clark, Brian S. [2 ]
Link, Brian A. [2 ]
Clarke, Jonathan D. W. [1 ]
机构
[1] Kings Coll London, MRC, Ctr Dev Neurobiol, London SE1 1UL, England
[2] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
apical polarisation; lumen formation; Pard3; Rablla; zebrafish; ADHERENS JUNCTIONS; SPINDLE ORIENTATION; RECYCLING ENDOSOME; CLEAVAGE FURROW; APICAL SURFACE; POLARITY; CENTROSOME; CYTOKINESIS; DIVISION; PROTEIN;
D O I
10.1038/emboj.2012.305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
By analysing the cellular and subcellular events that occur in the centre of the developing zebrafish neural rod, we have uncovered a novel mechanism of cell polarisation during lumen formation. Cells from each side of the neural rod interdigitate across the tissue midline. This is necessary for localisation of apical junctional proteins to the region where cells intersect the tissue midline. Cells assemble a mirror-symmetric microtubule cytoskeleton around the tissue midline, which is necessary for the trafficking of proteins required for normal lumen forma:ton, such as partitioning defective 3 and Rablla to this point. This occurs in advance and is independent of the midline cell division that has been shown to have a powerful role in lumen organisation. To our knowledge, this is the first example of the initiation of apical polarisation part way along the length of a cell, rather than at a cell extremity. Although the midline division is not necessary for apical polarisation, it confers a morphogenetic advantage by efficiently eliminating cellular processes that would otherwise bridge the developing lumen. The EMBO Journal (2013) 32, 30-44. doi:10.1038/emboj.2012.305; Published online 30 November 2012
引用
收藏
页码:30 / 44
页数:15
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