Literature DB >> 7037797

Chemotactic reorientation of granulocytes stimulated with micropipettes containing fMet-Leu-Phe.

G Gerisch, H U Keller.   

Abstract

Human granulocytes were stimulated by means of a micropipette, with an orifice of about 0.2 micrometer in diameter, which contained fMet-Leu-Phe at a concentration of 10(-5) M. The cells were reorientated by extending lamellipodia towards the source of the attractant, often within less than 10 s. Any part of the granulocyte, from the front to the tip of the tail, could be stimulated to produce new lamellipodia. Usually, but not always, this response occurred at the side of the cell nearest to the micropipette. Cells stimulated from behind responded in one of the following ways: (1) Cells that maintained their polarity extended new lamellipodia at one side of the leading front and reorientated by moving in a U-turn towards the micropipette. Occasionally, the leading front was split because one part of the front tried to make a left-hand and the other a right-hand turn. (2) Formation of lamellipodia at the leading front was arrested and new lamellipodia were formed at the tail instead, indicating reversal of polarity. The result was an immediate change in the direction of locomotion by about 180 degrees. (3) A combination of the first 2 forms of behaviour was observed occasionally. Transiently, lamellipodia were extended from cell surface areas both close to and distant from the micropipette. These observations show that parts of a cell can respond independently to chemotactic gradients by extending lamellipodia towards the source of the attractant. The phenomenon can easily be explained by assuming that a temporal change of attractant concentration is recognized.

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Year:  1981        PMID: 7037797     DOI: 10.1242/jcs.52.1.1

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  62 in total

1.  Dynamics of a chemoattractant receptor in living neutrophils during chemotaxis.

Authors:  G Servant; O D Weiner; E R Neptune; J W Sedat; H R Bourne
Journal:  Mol Biol Cell       Date:  1999-04       Impact factor: 4.138

2.  Spatial control of actin polymerization during neutrophil chemotaxis.

Authors:  O D Weiner; G Servant; M D Welch; T J Mitchison; J W Sedat; H R Bourne
Journal:  Nat Cell Biol       Date:  1999-06       Impact factor: 28.824

3.  Functions of LIM proteins in cell polarity and chemotactic motility.

Authors:  Bharat Khurana; Taruna Khurana; Nandkumar Khaire; Angelika A Noegel
Journal:  EMBO J       Date:  2002-10-15       Impact factor: 11.598

Review 4.  Microfluidic technologies for temporal perturbations of chemotaxis.

Authors:  Daniel Irimia
Journal:  Annu Rev Biomed Eng       Date:  2010-08-15       Impact factor: 9.590

5.  The cyclase-associated protein CAP as regulator of cell polarity and cAMP signaling in Dictyostelium.

Authors:  Angelika A Noegel; Rosemarie Blau-Wasser; Hameeda Sultana; Rolf Müller; Lars Israel; Michael Schleicher; Hitesh Patel; Cornelis J Weijer
Journal:  Mol Biol Cell       Date:  2003-10-31       Impact factor: 4.138

6.  Galvanotaxis of human granulocytes: electric field jump studies.

Authors:  K Franke; H Gruler
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

Review 7.  Understanding eukaryotic chemotaxis: a pseudopod-centred view.

Authors:  Robert H Insall
Journal:  Nat Rev Mol Cell Biol       Date:  2010-05-06       Impact factor: 94.444

8.  Subsecond reorganization of the actin network in cell motility and chemotaxis.

Authors:  Stefan Diez; Günther Gerisch; Kurt Anderson; Annette Müller-Taubenberger; Till Bretschneider
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-13       Impact factor: 11.205

9.  Biased random walk by stochastic fluctuations of chemoattractant-receptor interactions at the lower limit of detection.

Authors:  Peter J M van Haastert; Marten Postma
Journal:  Biophys J       Date:  2007-05-18       Impact factor: 4.033

10.  Cell-substrate interactions and locomotion of Dictyostelium wild-type and mutants defective in three cytoskeletal proteins: a study using quantitative reflection interference contrast microscopy.

Authors:  M Schindl; E Wallraff; B Deubzer; W Witke; G Gerisch; E Sackmann
Journal:  Biophys J       Date:  1995-03       Impact factor: 4.033

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