Polarization of Chemoattractant Receptor Signaling During Neutrophil Chemotaxis
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- Guy Servant
- Department of Cellular and Molecular Pharmacology and
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- Orion D. Weiner
- Department of Cellular and Molecular Pharmacology and
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- Paul Herzmark
- Department of Cellular and Molecular Pharmacology and
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- Tamás Balla
- Endocrinology and Reproduction Research Branch, National Institutes of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892–4510, USA.
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- John W. Sedat
- Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94143, USA.
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- Henry R. Bourne
- Department of Cellular and Molecular Pharmacology and
抄録
<jats:p> Morphologic polarity is necessary for chemotaxis of mammalian cells. As a probe of intracellular signals responsible for this asymmetry, the pleckstrin homology domain of the AKT protein kinase (or protein kinase B), tagged with the green fluorescent protein (PHAKT-GFP), was expressed in neutrophils. Upon exposure of cells to chemoattractant, PHAKT-GFP is recruited selectively to membrane at the cell's leading edge, indicating an internal signaling gradient that is much steeper than that of the chemoattractant. Translocation of PHAKT-GFP is inhibited by toxin-B from <jats:italic>Clostridium difficile</jats:italic> , indicating that it requires activity of one or more Rho guanosine triphosphatases. </jats:p>
収録刊行物
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- Science
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Science 287 (5455), 1037-1040, 2000-02-11
American Association for the Advancement of Science (AAAS)
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キーワード
詳細情報 詳細情報について
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- CRID
- 1362825894834893568
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- NII論文ID
- 80011642303
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- ISSN
- 10959203
- 00368075
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- データソース種別
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- Crossref
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