Complement Fragment C3a Controls Mutual Cell Attraction during Collective Cell Migration

被引:253
作者
Carmona-Fontaine, Carlos [1 ]
Theveneau, Eric [1 ]
Tzekou, Apostolia [4 ]
Tada, Masazumi [1 ]
Woods, Mae [1 ,2 ,3 ]
Page, Karen M. [2 ,3 ]
Parsons, Maddy [5 ]
Lambris, John D. [4 ]
Mayor, Roberto [1 ]
机构
[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
[2] UCL, Dept Math, London WC1E 6BT, England
[3] UCL, CoMPLEX, London WC1E 6BT, England
[4] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[5] Kings Coll London, Randall Div Cell & Mol Biophys, London WC2R 2LS, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 美国国家卫生研究院;
关键词
NEURAL CREST MIGRATION; IN-VIVO; EXPRESSION; XENOPUS; MORPHOGENESIS; DIVERSITY; MOVEMENTS; CADHERINS; MEMBRANE; INVASION;
D O I
10.1016/j.devcel.2011.10.012
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Collective cell migration is a mode of movement crucial for morphogenesis and cancer metastasis. However, little is known about how migratory cells coordinate collectively. Here we show that mutual cell-cell attraction (named here coattraction) is required to maintain cohesive clusters of migrating mesenchymal cells. Coattraction can counterbalance the natural tendency of cells to disperse via mechanisms such as contact inhibition and epithelial-to-mesenchymal transition. Neural crest cells are coattracted via the complement fragment C3a and its receptor C3aR, revealing an unexpected role of complement proteins in early vertebrate development. Loss of coattraction disrupts collective and coordinated movements of these cells. We propose that coattraction and contact inhibition act in concert to allow cell collectives to self-organize and respond efficiently to external signals, such as chemoattractants and repellents.
引用
收藏
页码:1026 / 1037
页数:12
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