Collective cell migration requires vesicular trafficking for chemoattractant delivery at the trailing edge

Author:

Kriebel Paul W.1,Barr Valarie A.1,Rericha Erin C.12,Zhang Guofeng3,Parent Carole A.1

Affiliation:

1. Laboratory of Cellular and Molecular Biology, National Cancer Institute,

2. Institute for Research in Electronics and Applied Physics, University of Maryland, College Park, MD 20742

3. Division of Bioengineering and Physical Sciences, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD 20892

Abstract

Chemoattractant signaling induces the polarization and directed movement of cells secondary to the activation of multiple effector pathways. In addition, chemotactic signals can be amplified and relayed to proximal cells via the synthesis and secretion of additional chemoattractant. The mechanisms underlying such remarkable features remain ill defined. We show that the asymmetrical distribution of adenylyl cyclase (ACA) at the back of Dictyostelium discoideum cells, an essential determinant of their ability to migrate in a head-to-tail fashion, requires vesicular trafficking. This trafficking results in a local accumulation of ACA-containing intracellular vesicles and involves intact actin, microtubule networks, and de novo protein synthesis. We also show that migrating cells leave behind ACA-containing vesicles, likely secreted as multivesicular bodies and presumably involved in the formation of head-to-tail arrays of migrating cells. We propose that similar compartmentalization and shedding mechanisms exist in mammalian cells during embryogenesis, wound healing, neuron growth, and metastasis.

Publisher

Rockefeller University Press

Subject

Cell Biology

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