Letter

Nature 448, 362-365 (19 July 2007) | doi:10.1038/nature05965; Received 29 April 2007; Accepted 25 May 2007

Two distinct modes of guidance signalling during collective migration of border cells

Ambra Bianco1, Minna Poukkula1,3, Adam Cliffe1,2,3, Juliette Mathieu1, Carlos M. Luque1,4, Tudor A. Fulga1,4 & Pernille Rørth1,2

  1. European Molecular Biology Laboratory, Heidelberg, 69117, Germany
  2. Temasek Life Sciences Laboratory (TLL), 1 Research Link, National University of Singapore, Singapore 117604
  3. These authors contributed equally to this work.
  4. Present addresses: Centro Andaluz de Biología del Desarrollo CSIC/UPO, Carretera de Utrera, Km. 1, 41013 Sevilla, Spain (C.M.L.); Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, 02115 Boston, USA (T.A.F.).

Correspondence to: Pernille Rørth1,2 Correspondence and requests for materials should be addressed to P.R. (Email: Pernille@tll.org.sg).

Although directed migration is a feature of both individual cells and cell groups, guided migration has been studied most extensively for single cells in simple environments1, 2. Collective guidance of cell groups remains poorly understood, despite its relevance for development and metastasis3. Neural crest cells and neuronal precursors migrate as loosely organized streams of individual cells4, 5, whereas cells of the fish lateral line6, 7, Drosophila tracheal tubes and border-cell clusters8 migrate as more coherent groups. Here we use Drosophila border cells to examine how collective guidance is performed. We report that border cells migrate in two phases using distinct mechanisms. Genetic analysis combined with live imaging shows that polarized cell behaviour is critical for the initial phase of migration, whereas dynamic collective behaviour dominates later. PDGF- and VEGF-related receptor and epidermal growth factor receptor act in both phases, but use different effector pathways in each. The myoblast city (Mbc, also known as DOCK180) and engulfment and cell motility (ELMO, also known as Ced-12) pathway is required for the early phase, in which guidance depends on subcellular localization of signalling within a leading cell. During the later phase, mitogen-activated protein kinase and phospholipase Cgamma are used redundantly, and we find that the cluster makes use of the difference in signal levels between cells to guide migration. Thus, information processing at the multicellular level is used to guide collective behaviour of a cell group.

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