Literature DB >> 7681007

Exocytosis of vacuolar apical compartment (VAC) in Madin-Darby canine kidney epithelial cells: cAMP is involved as second messenger.

M Brignoni1, E J Podesta, P Mele, M L Rodriguez, D E Vega-Salas, P J Salas.   

Abstract

Vacuolar apical compartment (VAC) is a transient organelle originally observed in Madin-Darby canine kidney (MDCK) epithelial cells impaired from forming cell-cell contacts. VACs are large vacuoles which contain microvilli and apical plasma membrane markers (among others, a 184-kDa plasma membrane protein, AP2), but exclude basolateral membrane markers. Upon reestablishment of cell-cell contacts, VACs are rapidly (within 1 h) exocytosed toward intercellular spaces, after which the apical plasma membrane drifts toward its final destination (Vega-Salas, Salas, and Rodriguez-Boulan. 1988. J. Cell Biol. 107, 1717-1728). In this work, we studied the role of cAMP as a mediator for the exocytosis of VACs. We shifted confluent cells from low to normal calcium medium (thus reestablishing cell-cell contacts and causing VAC exocytosis), a shift which resulted in a significant rise of cellular levels of both total intracellular and protein-bound cAMP. The 8-Br analog of cAMP (8-Br-cAMP) (5-50 microM) caused externalization of the intracellular compartment of AP2 as measured by radioimmunoassay. A similar effect was observed with 3-isobutyl-1-methylxanthine. 8-Br-cAMP also caused the appearance of AP2-positive VAC images in nonpermeabilized cells, namely, VACs that become accessible to extracellular antibodies upon fusion with the plasma membrane. Lanthanum, which abolishes the peak of intracellular free calcium during a calcium switch, failed to block the exocytosis. On the other hand, 12-O-tetradecanoylphorbol-13-acetate induced only a modest exocytic response. Finally, 8-Br-cAMP induced VAC exocytosis in sparse MDCK cells grown in normal calcium medium. These data indicate that cAMP is a mediator between the extracellular signal provided by cell-cell contacts and VAC exocytosis.

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Year:  1993        PMID: 7681007     DOI: 10.1006/excr.1993.1072

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  6 in total

1.  Intracellular redirection of plasma membrane trafficking after loss of epithelial cell polarity.

Authors:  S H Low; M Miura; P A Roche; A C Valdez; K E Mostov; T Weimbs
Journal:  Mol Biol Cell       Date:  2000-09       Impact factor: 4.138

2.  A molecular network for de novo generation of the apical surface and lumen.

Authors:  David M Bryant; Anirban Datta; Alejo E Rodríguez-Fraticelli; Johan Peränen; Fernando Martín-Belmonte; Keith E Mostov
Journal:  Nat Cell Biol       Date:  2010-10-03       Impact factor: 28.824

3.  Mechanism of IFN-gamma-induced endocytosis of tight junction proteins: myosin II-dependent vacuolarization of the apical plasma membrane.

Authors:  Markus Utech; Andrei I Ivanov; Stanislav N Samarin; Matthias Bruewer; Jerrold R Turner; Randall J Mrsny; Charles A Parkos; Asma Nusrat
Journal:  Mol Biol Cell       Date:  2005-07-29       Impact factor: 4.138

4.  Sphingolipid transport to the apical plasma membrane domain in human hepatoma cells is controlled by PKC and PKA activity: a correlation with cell polarity in HepG2 cells.

Authors:  M M Zegers; D Hoekstra
Journal:  J Cell Biol       Date:  1997-07-28       Impact factor: 10.539

5.  Temporal Coordination of Collective Migration and Lumen Formation by Antagonism between Two Nuclear Receptors.

Authors:  Xianping Wang; Heng Wang; Lin Liu; Sheng Li; Gregory Emery; Jiong Chen
Journal:  iScience       Date:  2020-07-01

Review 6.  Regulation of organic anion transport in the liver.

Authors:  H Roelofsen; M Müller; P L Jansen
Journal:  Yale J Biol Med       Date:  1997 Jul-Aug
  6 in total

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