Literature DB >> 3978702

Reorientation of the Golgi apparatus and the microtubule-organizing center inside macrophages subjected to a chemotactic gradient.

I Nemere, A Kupfer, S J Singer.   

Abstract

Mouse peritoneal macrophages subjected to gradients of activated mouse serum were found by immunofluorescence observations to have their Golgi apparatus and their microtubule-organizing center largely oriented in the direction of the gradient. By analogy with similar results obtained with motile fibroblasts, it is proposed that these two organelles are rapidly and coordinately reoriented inside the macrophages in order to direct the insertion of new membrane mass, via vesicles derived from the Golgi apparatus, into the leading edge of the cell. Consistent with the importance of such membrane insertion to cell migration, we found that the ionophore monensin, an inhibitor of Golgi functions, inhibited cell motility in the chemostactic gradient. It was further shown that several inhibitors of chemotaxis (monensin, cytochalasin D, cycloheximide) did not inhibit the reorientation of the Golgi apparatus/microtubule-organizing center in cells exposed to a chemotactic gradient, and that the reorientation required extracellular Ca+2.

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Year:  1985        PMID: 3978702     DOI: 10.1002/cm.970050103

Source DB:  PubMed          Journal:  Cell Motil        ISSN: 0271-6585


  15 in total

1.  Rear polarization of the microtubule-organizing center in neointimal smooth muscle cells depends on PKCα, ARPC5, and RHAMM.

Authors:  Rosalind Silverman-Gavrila; Lorelei Silverman-Gavrila; Guangpei Hou; Ming Zhang; Milton Charlton; Michelle P Bendeck
Journal:  Am J Pathol       Date:  2011-02       Impact factor: 4.307

2.  MTOC reorientation occurs during FcgammaR-mediated phagocytosis in macrophages.

Authors:  Edward W Eng; Adam Bettio; John Ibrahim; Rene E Harrison
Journal:  Mol Biol Cell       Date:  2007-04-18       Impact factor: 4.138

Review 3.  Orientation and function of the nuclear-centrosomal axis during cell migration.

Authors:  G W Gant Luxton; Gregg G Gundersen
Journal:  Curr Opin Cell Biol       Date:  2011-08-30       Impact factor: 8.382

4.  SMRT analysis of MTOC and nuclear positioning reveals the role of EB1 and LIC1 in single-cell polarization.

Authors:  Christopher M Hale; Wei-Chiang Chen; Shyam B Khatau; Brian R Daniels; Jerry S H Lee; Denis Wirtz
Journal:  J Cell Sci       Date:  2011-12-22       Impact factor: 5.285

5.  An on-chip study on the influence of geometrical confinement and chemical gradient on cell polarity.

Authors:  Wenfu Zheng; Yunyan Xie; Kang Sun; Dong Wang; Yi Zhang; Chen Wang; Yong Chen; Xingyu Jiang
Journal:  Biomicrofluidics       Date:  2014-10-15       Impact factor: 2.800

6.  The centrosome neither persistently leads migration nor determines the site of axonogenesis in migrating neurons in vivo.

Authors:  Martin Distel; Jennifer C Hocking; Katrin Volkmann; Reinhard W Köster
Journal:  J Cell Biol       Date:  2010-11-08       Impact factor: 10.539

7.  Mitochondrial localization and the persistent migration of epithelial cancer cells.

Authors:  Salil P Desai; Sangeeta N Bhatia; Mehmet Toner; Daniel Irimia
Journal:  Biophys J       Date:  2013-05-07       Impact factor: 4.033

8.  A role for PP1/NIPP1 in steering migration of human cancer cells.

Authors:  Cristina Martin-Granados; Alan R Prescott; Nele Van Dessel; Aleyde Van Eynde; Miguel Arocena; Izabela P Klaska; Janina Görnemann; Monique Beullens; Mathieu Bollen; John V Forrester; Colin D McCaig
Journal:  PLoS One       Date:  2012-07-16       Impact factor: 3.240

9.  The reorganization of microfilaments, centrosomes, and microtubules during in vitro small wound reendothelialization.

Authors:  M K Wong; A I Gotlieb
Journal:  J Cell Biol       Date:  1988-11       Impact factor: 10.539

10.  A microtubule-binding protein associated with membranes of the Golgi apparatus.

Authors:  V J Allan; T E Kreis
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

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