Cells display chemotaxis and electrotaxis by migrating directionally in gradients of specific chemicals or electrical potential. Chemotaxis in Dictyostelium discoideum is mediated by G protein–coupled receptors. The unique Gβ is essential for all chemotactic responses, although different chemoattractants use different receptors and Gα subunits. Dictyostelium amoebae show striking electrotaxis in an applied direct current electric field. Perhaps electrotaxis and chemotaxis share similar signaling mechanisms? Null mutation of Gβ and cAMP receptor 1 and Gα2 did not abolish electrotaxis, although Gβ-null mutations showed suppressed electrotaxis. By contrast, G protein signaling plays an essential role in chemotaxis. G protein–coupled receptor signaling was monitored with PHcrac–green fluorescent protein, which translocates to inositol phospholipids at the leading edge of cells during chemotaxis. There was no intracellular gradient of this protein during electrotaxis. However, F-actin was polymerized at the leading edge of cells during electrotaxis. We conclude that reception and transduction of the electrotaxis signal are largely independent of G protein–coupled receptor signaling and that the pathways driving chemotaxis and electrotaxis intersect downstream of heterotrimeric G proteins to invoke cytoskeletal elements.
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10 June 2002
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June 03 2002
Genetic analysis of the role of G protein–coupled receptor signaling in electrotaxis
Min Zhao,
Min Zhao
1Department of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
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Tian Jin,
Tian Jin
2Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, MD 21205
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Colin D. McCaig,
Colin D. McCaig
1Department of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
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John V. Forrester,
John V. Forrester
3Department of Ophthalmology, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
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Peter N. Devreotes
Peter N. Devreotes
2Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, MD 21205
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Min Zhao
1Department of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
Tian Jin
2Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, MD 21205
Colin D. McCaig
1Department of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
John V. Forrester
3Department of Ophthalmology, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom
Peter N. Devreotes
2Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, MD 21205
Address correspondence to Min Zhao, Dept. of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK. Tel.: 44-1224-273001. Fax: 44-1224-273019. E-mail: [email protected]
The online version of this article contains supplemental material.
T. Jin's present address is Laboratory of Immunogenetics, NIH-NIAID, Twinbrook II Facility, 12441 Parklawn Dr., Rockville, MD 20852.
*
Abbreviations used in this paper: DC, direct current; EF, electric field; GFP, green fluorescent protein; PH, pleckstrin homology.
Received:
December 17 2001
Revision Received:
April 16 2002
Accepted:
April 16 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2002
J Cell Biol (2002) 157 (6): 921–928.
Article history
Received:
December 17 2001
Revision Received:
April 16 2002
Accepted:
April 16 2002
Citation
Min Zhao, Tian Jin, Colin D. McCaig, John V. Forrester, Peter N. Devreotes; Genetic analysis of the role of G protein–coupled receptor signaling in electrotaxis . J Cell Biol 10 June 2002; 157 (6): 921–928. doi: https://doi.org/10.1083/jcb.200112070
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