Literature DB >> 6889606

Reevaluation of brush border motility: calcium induces core filament solution and microvillar vesiculation.

D R Burgess, B E Prum.   

Abstract

The report that microvillar cores of isolated, demembranated brush borders retract into the terminal web in the presence of Ca(++) and ATP has been widely cited as an example of Ca(++)-regulated nonmuscle cell motility. Because of recent findings that microvillar core actin filaments are cross-linked by villin which, in the presence of micromolar Ca(++), fragments actin filaments, we used the techniques of video enhanced differential interference contrast, immunofluorescence, and phase contrast microscopy and thin-section electron microscopy (EM) to reexamine the question of contraction of isolated intestinal cell brush borders. Analysis of video enhanced light microscopic images of Triton- demembranated brush borders treated with a buffered Ca(++) solution shows the cores disintegrating with the terminal web remaining intact; membranated brush borders show the microvilli to vesiculate with Ca(++). Using Ca(++)/EGTA buffers, it is found that micromolar free Ca(++) causes core filament dissolution in membranated or demembranated brush borders, Ca(++) causes microvillar core solation followed by complete vesiculation of the microvillar membrane. The lengths of microvilli cores and rootlets were measured in thin sections of membranated and demembranated controls, in Ca(++)-, Ca(++) + ATP-, and in ATP-treated brush borders. Results of these measurements show that Ca(++) alone causes the complete solation of the microvillar cores, yet the rootlets in the terminal web region remain of normal length. These results show that microvilli do not retract into the terminal web in response to Ca(++) and ATP but rather that the microvillar cores disintegrate. NBD-phallicidin localization of actin and fluorescent antibodies to myosin reveal a circumferential band of actin and myosin in mildly permeabilized cells in the region of the junctional complex. The presence of these contractile proteins in this region, where other studies have shown a circumferential band of thin filaments, is consistent with the hypothesis that brush borders may be motile through the circumferential constriction of this "contractile ring," and is also consistent with the observations that ATP-treated brush borders become cup shaped as if there had been a circumferential constriction.

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Year:  1982        PMID: 6889606      PMCID: PMC2112202          DOI: 10.1083/jcb.94.1.97

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


  22 in total

1.  The visualization of actin filament polarity in thin sections. Evidence for the uniform polarity of membrane-associated filaments.

Authors:  D A Begg; R Rodewald; L I Rebhun
Journal:  J Cell Biol       Date:  1978-12       Impact factor: 10.539

2.  Organization of the cross-filaments in intestinal microvilli.

Authors:  P T Matsudaira; D R Burgess
Journal:  J Cell Biol       Date:  1982-03       Impact factor: 10.539

3.  Localization of actin and microfilament-associated proteins in the microvilli and terminal web of the intestinal brush border by immunofluorescence microscopy.

Authors:  A Bretscher; K Weber
Journal:  J Cell Biol       Date:  1978-12       Impact factor: 10.539

4.  The terminal web. A reevaluation of its structure and function.

Authors:  B E Hull; L A Staehelin
Journal:  J Cell Biol       Date:  1979-04       Impact factor: 10.539

5.  Brush border motility. Microvillar contraction in triton-treated brush borders isolated from intestinal epithelium.

Authors:  M S Mooseker
Journal:  J Cell Biol       Date:  1976-11       Impact factor: 10.539

6.  Organization of an actin filament-membrane complex. Filament polarity and membrane attachment in the microvilli of intestinal epithelial cells.

Authors:  M S Mooseker; L G Tilney
Journal:  J Cell Biol       Date:  1975-12       Impact factor: 10.539

7.  alpha-Actinin localization in the junctional complex of intestinal epithelial cells.

Authors:  S W Craig; J V Pardo
Journal:  J Cell Biol       Date:  1979-01       Impact factor: 10.539

8.  Characterization and localization of myosin in the brush border of intestinal epithelial cells.

Authors:  M S Mooseker; T D Pollard; K Fujiwara
Journal:  J Cell Biol       Date:  1978-11       Impact factor: 10.539

9.  Identification and organization of the components in the isolated microvillus cytoskeleton.

Authors:  P T Matsudaira; D R Burgess
Journal:  J Cell Biol       Date:  1979-12       Impact factor: 10.539

10.  Alpha-actinin localization in the cleavage furrow during cytokinesis.

Authors:  K Fujiwara; M E Porter; T D Pollard
Journal:  J Cell Biol       Date:  1978-10       Impact factor: 10.539

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  27 in total

1.  Calpain regulates enterocyte brush border actin assembly and pathogenic Escherichia coli-mediated effacement.

Authors:  David A Potter; Anjaiah Srirangam; Kerry A Fiacco; Daniel Brocks; John Hawes; Carter Herndon; Masatoshi Maki; David Acheson; Ira M Herman
Journal:  J Biol Chem       Date:  2003-05-22       Impact factor: 5.157

2.  Structural and functional lesions in brush border of human polarized intestinal Caco-2/TC7 cells infected by members of the Afa/Dr diffusely adhering family of Escherichia coli.

Authors:  I Peiffer; J Guignot; A Barbat; C Carnoy; S L Moseley; B J Nowicki; A L Servin; M F Bernet-Camard
Journal:  Infect Immun       Date:  2000-10       Impact factor: 3.441

3.  Adhesion of enteropathogenic Escherichia coli to human intestinal enterocytes and cultured human intestinal mucosa.

Authors:  S Knutton; D R Lloyd; A S McNeish
Journal:  Infect Immun       Date:  1987-01       Impact factor: 3.441

4.  Morphological alterations and cytoskeletal reorganization in opossum kidney (OK) cells during osmotic swelling and volume regulation.

Authors:  P C Dartsch; H A Kolb; M Beckmann; F Lang
Journal:  Histochemistry       Date:  1994-08

5.  Evidence for the association of villin with core filaments and rootlets of intestinal epithelial microvilli.

Authors:  D Drenckhahn; H D Hofmann; H G Mannherz
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

6.  Cell surface changes during mitosis and cytokinesis of epithelial cells.

Authors:  J M Sanger; A M Reingold; J W Sanger
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

7.  Pathogenicity of the diffusely adhering strain Escherichia coli C1845: F1845 adhesin-decay accelerating factor interaction, brush border microvillus injury, and actin disassembly in cultured human intestinal epithelial cells.

Authors:  M F Bernet-Camard; M H Coconnier; S Hudault; A L Servin
Journal:  Infect Immun       Date:  1996-06       Impact factor: 3.441

8.  Parathyroid hormone-induced changes of the brush border topography and cytoskeleton in cultured renal proximal tubular cells.

Authors:  M S Goligorsky; D N Menton; K A Hruska
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

9.  Myosin-1a is critical for normal brush border structure and composition.

Authors:  Matthew J Tyska; Andrew T Mackey; Jian-Dong Huang; Neil G Copeland; Nancy A Jenkins; Mark S Mooseker
Journal:  Mol Biol Cell       Date:  2005-03-09       Impact factor: 4.138

10.  Ultrastructural changes in lactating tissue related to the suppression of milk secretion by concanavalin A.

Authors:  U Welsch; S Singh; B H Stemberger; W Buchheim; S Patton
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

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