Literature DB >> 2681225

The response of the Golgi complex to microtubule alterations: the roles of metabolic energy and membrane traffic in Golgi complex organization.

J R Turner1, A M Tartakoff.   

Abstract

A striking example of the interrelation between the Golgi complex (GC) and microtubules is the reversible fragmentation and dispersal of the GC which occurs upon microtubule depolymerization. We have characterized dispersal of the GC after nocodazole treatment as well as its recovery from the dispersed state by immunofluorescent localization of beta 1, 4-galactosyltransferase in Madin-Darby bovine kidney cells. Immunofluorescent anti-tubulin staining allowed simultaneous examination of the microtubule array. Based on our results, dispersal can be divided into a three-step process: microtubule depolymerization, GC fragmentation, and fragment dispersal. In cells treated with metabolic inhibitors after microtubule depolymerization, neither fragmentation nor dispersal occur, despite the absence of assembled microtubules. Thus, fragmentation is energy dependent and not tightly linked to microtubule depolymerization. The slowing of fragmentation and dispersal by monensin or ammonium chloride, as well as progressive inhibition at less than 34 degrees C, suggest that ongoing membrane traffic is required for these processes. Similarly, recovery may be separated into four steps: microtubule depolymerization, GC fragment centralization, fragment coalescence, and polarization of the reticular GC network. Fragment centralization and coalescence were arrested by metabolic inhibitors, despite the presence of microtubules. Neither monensin nor ammonium choride inhibited GC recovery. Partial inhibition of recovery at reduced temperatures paralleled the extent of microtubule assembly. These data demonstrate that dispersal and recovery are multi-step operations, and that the individual steps differ in temperature dependence, energy dependence, and sensitivity to ionic perturbation. GC distribution and microtubule status have also been clearly dissociate, thereby proving that organization of the GC is an active process that is not simply determined by microtubule binding. Furthermore, the results indicate that ongoing intra-GC membrane traffic may participate in fragmentation and dispersal.

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Year:  1989        PMID: 2681225      PMCID: PMC2115848          DOI: 10.1083/jcb.109.5.2081

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  45 in total

1.  Microtubule stability and assembly in living cells: the influence of metabolic inhibitors, taxol and pH.

Authors:  M De Brabander; G Geuens; R Nuydens; R Willebrords; J De Mey
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1982

2.  Disparate effects of monensin and colchicine on intracellular processing of secretory proteins in cultured rat hepatocytes.

Authors:  K Oda; Y Misumi; Y Ikehara
Journal:  Eur J Biochem       Date:  1983-09-15

3.  Monoclonal antibodies that recognize discrete forms of tubulin.

Authors:  I Gozes; C J Barnstable
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

Review 4.  Perturbation of vesicular traffic with the carboxylic ionophore monensin.

Authors:  A M Tartakoff
Journal:  Cell       Date:  1983-04       Impact factor: 41.582

5.  Polarization of the Golgi apparatus and the microtubule-organizing center in cultured fibroblasts at the edge of an experimental wound.

Authors:  A Kupfer; D Louvard; S J Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

6.  Cold and metabolic inhibitor effects on cytoplasmic microtubules and the Golgi complex in cultured rat epiphyseal chondrocytes.

Authors:  S Moskalewski; J Thyberg; U Friberg
Journal:  Cell Tissue Res       Date:  1980       Impact factor: 5.249

7.  Binding and internalization of alpha 2-microglobulin by cultured fibroblasts. Effects of monovalent ionophores.

Authors:  R B Dickson; R Schlegel; M C Willingham; I Pastan
Journal:  Exp Cell Res       Date:  1982-11       Impact factor: 3.905

8.  Internalization of cationized ferritin into the Golgi complex of cultured mouse peritoneal macrophages. Effects of colchicine and cytochalasin B.

Authors:  J Thyberg
Journal:  Eur J Cell Biol       Date:  1980-12       Impact factor: 4.492

9.  Immunofluorescence microscopy of organized microtubule arrays in structurally stabilized meristematic plant cells.

Authors:  S M Wick; R W Seagull; M Osborn; K Weber; B E Gunning
Journal:  J Cell Biol       Date:  1981-06       Impact factor: 10.539

10.  Immunocytochemical localization of galactosyltransferase in HeLa cells: codistribution with thiamine pyrophosphatase in trans-Golgi cisternae.

Authors:  J Roth; E G Berger
Journal:  J Cell Biol       Date:  1982-04       Impact factor: 10.539

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  68 in total

1.  Low cytoplasmic pH causes fragmentation and dispersal of the Golgi apparatus in human hepatoma cells.

Authors:  T Yoshida; T Kamiya; K Imanaka-Yoshida; T Sakakura
Journal:  Int J Exp Pathol       Date:  1999-02       Impact factor: 1.925

2.  Golgi complex reorganization during muscle differentiation: visualization in living cells and mechanism.

Authors:  Z Lu; D Joseph; E Bugnard; K J Zaal; E Ralston
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

3.  The Golgi complex is a microtubule-organizing organelle.

Authors:  K Chabin-Brion; J Marceiller; F Perez; C Settegrana; A Drechou; G Durand; C Poüs
Journal:  Mol Biol Cell       Date:  2001-07       Impact factor: 4.138

4.  Identification of a novel light intermediate chain (D2LIC) for mammalian cytoplasmic dynein 2.

Authors:  Paula M Grissom; Eugeni A Vaisberg; J Richard McIntosh
Journal:  Mol Biol Cell       Date:  2002-03       Impact factor: 4.138

5.  Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis.

Authors:  N K Gonatas; A Stieber; Z Mourelatos; Y Chen; J O Gonatas; S H Appel; A P Hays; W F Hickey; J J Hauw
Journal:  Am J Pathol       Date:  1992-03       Impact factor: 4.307

6.  Distinct pathways for basolateral targeting of membrane and secretory proteins in polarized epithelial cells.

Authors:  W Boll; J S Partin; A I Katz; M J Caplan; J D Jamieson
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

7.  The hydrophobic domain of infectious bronchitis virus E protein alters the host secretory pathway and is important for release of infectious virus.

Authors:  Travis R Ruch; Carolyn E Machamer
Journal:  J Virol       Date:  2010-11-03       Impact factor: 5.103

8.  Altered Golgi apparatus in hydrostatically loaded articular cartilage chondrocytes.

Authors:  J J Parkkinen; M J Lammi; A Pelttari; H J Helminen; M Tammi; I Virtanen
Journal:  Ann Rheum Dis       Date:  1993-03       Impact factor: 19.103

9.  The hypolipidemic compound cetaben induces changes in Golgi morphology and vesicle movement.

Authors:  Werner J Kovacs; Michael Schrader; Ingrid Walter; Herbert Stangl
Journal:  Histochem Cell Biol       Date:  2004-07-28       Impact factor: 4.304

10.  The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease.

Authors:  Z Mourelatos; N K Gonatas; A Stieber; M E Gurney; M C Dal Canto
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

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