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Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover.

Publication ,  Journal Article
Volovyk, ZM; Wolf, MJ; Prasad, SVN; Rockman, HA
Published in: J Biol Chem
April 7, 2006

Stimulation of beta-adrenergic receptors (betaARs) leads to sequential recruitment of beta-arrestin, AP-2 adaptor protein, clathrin, and dynamin to the receptor complex, resulting in endocytosis. Whether a dynamic actin cytoskeleton is required for betaAR endocytosis is not known. In this study, we have used beta(1)- and beta(2) ARs, two ubiquitously expressed members of the betaAR family, to comprehensively evaluate the requirement of the actin cytoskeleton in receptor internalization. The integrity of the actin cytoskeleton was manipulated with the agent latrunculin B (LB) and mutants of cofilin to depolymerize actin filaments. Treatment of cells with LB resulted in dose-dependent depolymerization of the cortical actin cytoskeleton that was associated with significant attenuation in internalization of beta(2)ARs, beta(1)ARs, and mutants of beta(1)ARs that internalize via either clathrin- or caveolin-dependent pathways. Importantly, LB treatment did not inhibit beta-arrestin translocation or dynamin recruitment to the agonist-stimulated receptor. To unequivocally demonstrate the requirement of the actin cytoskeleton for beta(2)AR endocytosis, we used an actin-binding protein cofilin that biochemically depolymerizes and severs actin filaments. Isoproterenol-mediated internalization of beta(2)AR was completely blocked in the presence of wild type cofilin, which could be rescued by a mutant of cofilin that mimics a constitutive phosphorylated state and leads to normal agonist-stimulated beta(2)AR endocytosis. Finally, treatment with jasplakinolide, an inhibitor of actin turnover, resulted in dose-dependent inhibition of beta(2)AR internalization, suggesting that turnover of actin filaments at the receptor complex is required for endocytosis. Taken together, these data demonstrate that intact and functional dynamic actin cytoskeleton is required for normal betaAR internalization.

Duke Scholars

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

April 7, 2006

Volume

281

Issue

14

Start / End Page

9773 / 9780

Location

United States

Related Subject Headings

  • Thiazolidines
  • Thiazoles
  • Receptors, Adrenergic, beta-2
  • Receptors, Adrenergic, beta-1
  • Kidney
  • Isoproterenol
  • Humans
  • Endocytosis
  • Cell Culture Techniques
  • Bridged Bicyclo Compounds, Heterocyclic
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Volovyk, Z. M., Wolf, M. J., Prasad, S. V. N., & Rockman, H. A. (2006). Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover. J Biol Chem, 281(14), 9773–9780. https://doi.org/10.1074/jbc.M511435200
Volovyk, Zoya M., Matthew J. Wolf, Sathyamangla V Naga Prasad, and Howard A. Rockman. “Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover.J Biol Chem 281, no. 14 (April 7, 2006): 9773–80. https://doi.org/10.1074/jbc.M511435200.
Volovyk ZM, Wolf MJ, Prasad SVN, Rockman HA. Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover. J Biol Chem. 2006 Apr 7;281(14):9773–80.
Volovyk, Zoya M., et al. “Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover.J Biol Chem, vol. 281, no. 14, Apr. 2006, pp. 9773–80. Pubmed, doi:10.1074/jbc.M511435200.
Volovyk ZM, Wolf MJ, Prasad SVN, Rockman HA. Agonist-stimulated beta-adrenergic receptor internalization requires dynamic cytoskeletal actin turnover. J Biol Chem. 2006 Apr 7;281(14):9773–9780.

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

April 7, 2006

Volume

281

Issue

14

Start / End Page

9773 / 9780

Location

United States

Related Subject Headings

  • Thiazolidines
  • Thiazoles
  • Receptors, Adrenergic, beta-2
  • Receptors, Adrenergic, beta-1
  • Kidney
  • Isoproterenol
  • Humans
  • Endocytosis
  • Cell Culture Techniques
  • Bridged Bicyclo Compounds, Heterocyclic