8
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Moving towards a paradigm: common mechanisms of chemotactic signaling in Dictyostelium and mammalian leukocytes.

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Chemotaxis, or directed migration of cells along a chemical gradient, is a highly coordinated process that involves gradient sensing, motility, and polarity. Most of our understanding of chemotaxis comes from studies of cells undergoing amoeboid-type migration, in particular the social amoeba Dictyostelium discoideum and leukocytes. In these amoeboid cells the molecular events leading to directed migration can be conceptually divided into four interacting networks: receptor/G protein, signal transduction, cytoskeleton, and polarity. The signal transduction network occupies a central position in this scheme as it receives direct input from the receptor/G protein network, as well as feedback from the cytoskeletal and polarity networks. Multiple overlapping modules within the signal transduction network transmit the signals to the actin cytoskeleton network leading to biased pseudopod protrusion in the direction of the gradient. The overall architecture of the networks, as well as the individual signaling modules, is remarkably conserved between Dictyostelium and mammalian leukocytes, and the similarities and differences between the two systems are the subject of this review.

          Related collections

          Author and article information

          Journal
          Cell. Mol. Life Sci.
          Cellular and molecular life sciences : CMLS
          1420-9071
          1420-682X
          Oct 2014
          : 71
          : 19
          Affiliations
          [1 ] Department of Cell Biology, Johns Hopkins University, School of Medicine, 725 N. Wolfe St., 114 WBSB, Baltimore, MD, 21205, USA.
          Article
          NIHMS597547
          10.1007/s00018-014-1638-8
          4162842
          24846395
          7731caa0-38d2-46c5-85f0-47e39f4d4363
          History

          Comments

          Comment on this article