The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance

被引:133
作者
Ackley, BD
Crew, JR
Elamaa, H
Pihlajaniemi, T
Kuo, CJ
Kramer, JM
机构
[1] Northwestern Univ, Sch Med, Dept Cell & Mol Biol, Chicago, IL 60611 USA
[2] Univ Oulu, Bioctr, Collagen Res Unit, FIN-90014 Oulu, Finland
[3] Univ Oulu, Dept Med Biochem, FIN-90014 Oulu, Finland
[4] Harvard Univ, Sch Med, Childrens Hosp, Dept Surg, Boston, MA 02115 USA
关键词
cell migration; neurogenesis; endostatin; collagen; Caenorhahditis elegans;
D O I
10.1083/jcb.152.6.1219
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Type XVIII collagen is a homotrimeric basement membrane molecule of unknown function, whose COOH-terminal NC1 domain contains endostatin (ES), a potent antiangiogenic agent. The Caenorhabditis elegans collagen XVIII homologue, cle-1, encodes three developmentally regulated protein isoforms expressed predominantly in neurons. The CLE-1 protein is found in low amounts in all basement membranes but accumulates at high levels in the nervous system. Deletion of the cle-1 NC1 domain results in viable fertile animals that display multiple cell migration and axon guidance defects. Particular defects can be rescued by ectopic expression of the NC1 domain, which is shown to be capable of forming trimers. In contrast, expression of monomeric ES does not rescue but dominantly causes cell and axon migration defects that phenocopy the NC1 deletion, suggesting that ES inhibits the promigratory activity of the NC1 domain. These results indicate that the cle-1 NC1/ES domain regulates cell and axon migrations in C. elegans.
引用
收藏
页码:1219 / 1232
页数:14
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