Drosophila syndecan regulates tracheal cell migration by stabilizing Robo levels

被引:8
|
作者
Schulz, Joachim G. [1 ,2 ,3 ]
Ceulemans, Helga [1 ,3 ]
Caussinus, Emmanuel [4 ]
Baietti, Maria F. [1 ,3 ]
Affolter, Markus [4 ]
Hassan, Bassem A. [2 ,3 ]
David, Guido [1 ,3 ]
机构
[1] Katholieke Univ Leuven, Lab Glycobiol & Dev Genet, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven VIB, Neurogenet Lab, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Dept Human Genet, Ctr Human Genet, B-3000 Louvain, Belgium
[4] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
cell migration; Drosophila; heparan sulphate; Robo; tracheal system; HEPARAN-SULFATE PROTEOGLYCAN; BRANCHING MORPHOGENESIS; AXON GUIDANCE; SLIT; SURFACE; MIDLINE; COMMISSURELESS; ANGIOGENESIS; ACTIVATION; MECHANISMS;
D O I
10.1038/embor.2011.153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we identify a new role for Syndecan (Sdc), the only transmembrane heparan sulphate proteoglycan in Drosophila, in tracheal development. Sdc is required cell autonomously for efficient directed migration and fusion of dorsal branch cells, but not for dorsal branch formation per se. The cytoplasmic domain of Sdc is dispensable, indicating that Sdc does not transduce a signal by itself. Although the branch-specific phenotype of sdc mutants resembles those seen in the absence of Slit/Robo2 signalling, genetic interaction experiments indicate that Sdc also helps to suppress Slit/Robo2 signalling. We conclude that Sdc cell autonomously regulates Slit/Robo2 signalling in tracheal cells to guarantee ordered directional migration and branch fusion.
引用
收藏
页码:1039 / 1046
页数:8
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