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12 facilitates shortening in human airway smooth muscle by modulating phosphoinositide 3-kinase-mediated activation in a RhoA-dependent manner.
Yoo, Edwin J; Cao, Gaoyuan; Koziol-White, Cynthia J; Ojiaku, Christie A; Sunder, Krishna; Jude, Joseph A; Michael, James V; Lam, Hong; Pushkarsky, Ivan; Damoiseaux, Robert; Di Carlo, Dino; Ahn, Kwangmi; An, Steven S; Penn, Raymond B; Panettieri, Reynold A.
Afiliação
  • Yoo EJ; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Cao G; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Koziol-White CJ; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Ojiaku CA; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Sunder K; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Jude JA; Rutgers Institute for Translational Medicine and Science, Child Health Institute, Rutgers University, New Brunswick, NJ, USA.
  • Michael JV; Department of Medicine, Division of Pulmonary and Critical Care Medicine, Center for Translational Medicine, Jane and Leonard Korman Lung Center, Thomas Jefferson University, Philadelphia, PA, USA.
  • Lam H; Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Pushkarsky I; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Damoiseaux R; Department of Molecular and Medicinal Pharmacology, University of California, Los Angeles, CA, USA.
  • Di Carlo D; California NanoSystems Institute, University of California, Los Angeles, CA, USA.
  • Ahn K; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • An SS; California NanoSystems Institute, University of California, Los Angeles, CA, USA.
  • Penn RB; Department of Mechanical Engineering, University of California, Los Angeles, CA, USA.
  • Panettieri RA; National Institute of Mental Health, Bethesda, MD, USA.
Br J Pharmacol ; 174(23): 4383-4395, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28921504
ABSTRACT
BACKGROUND AND

PURPOSE:

PI3K-dependent activation of Rho kinase (ROCK) is necessary for agonist-induced human airway smooth muscle cell (HASMC) contraction, and inhibition of PI3K promotes bronchodilation of human small airways. The mechanisms driving agonist-mediated PI3K/ROCK axis activation, however, remain unclear. Given that G12 family proteins activate ROCK pathways in other cell types, their role in M3 muscarinic acetylcholine receptor-stimulated PI3K/ROCK activation and contraction was examined. EXPERIMENTAL

APPROACH:

Gα12 coupling was evaluated using co-immunoprecipitation and serum response element (SRE)-luciferase reporter assays. siRNA and pharmacological approaches, as well as overexpression of a regulator of G-protein signaling (RGS) proteins were applied in HASMCs. Phosphorylation levels of Akt, myosin phosphatase targeting subunit-1 (MYPT1), and myosin light chain-20 (MLC) were measured. Contraction and shortening were evaluated using magnetic twisting cytometry (MTC) and micro-pattern deformation, respectively. Human precision-cut lung slices (hPCLS) were utilized to evaluate bronchoconstriction. KEY

RESULTS:

Knockdown of M3 receptors or Gα12 attenuated activation of Akt, MYPT1, and MLC phosphorylation. Gα12 coimmunoprecipitated with M3 receptors, and p115RhoGEF-RGS overexpression inhibited carbachol-mediated induction of SRE-luciferase reporter. p115RhoGEF-RGS overexpression inhibited carbachol-induced activation of Akt, HASMC contraction, and shortening. Moreover, inhibition of RhoA blunted activation of PI3K. Lastly, RhoA inhibitors induced dilation of hPCLS. CONCLUSIONS AND IMPLICATIONS Gα12 plays a crucial role in HASMC contraction via RhoA-dependent activation of the PI3K/ROCK axis. Inhibition of RhoA activation induces bronchodilation in hPCLS, and targeting Gα12 signaling may elucidate novel therapeutic targets in asthma. These findings provide alternative approaches to the clinical management of airway obstruction in asthma.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína rhoA de Ligação ao GTP / Subunidades alfa G12-G13 de Proteínas de Ligação ao GTP / Fosfatidilinositol 3-Quinase / Músculo Liso Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína rhoA de Ligação ao GTP / Subunidades alfa G12-G13 de Proteínas de Ligação ao GTP / Fosfatidilinositol 3-Quinase / Músculo Liso Idioma: En Ano de publicação: 2017 Tipo de documento: Article