TGF-β1 Evokes Human Airway Smooth Muscle Cell Shortening and Hyperresponsiveness via Smad3

Autor: Steven S. An, Edwin J. Yoo, Reynold A. Panettieri, Gaoyuan Cao, Wanqu Zhu, Christie A. Ojiaku, Blanca E. Himes, Maya Shumyatcher
Rok vydání: 2018
Předmět:
0301 basic medicine
Pulmonary and Respiratory Medicine
Myosin Light Chains
Myosin light-chain kinase
Bronchoconstriction
medicine.medical_treatment
Myocytes
Smooth Muscle

Clinical Biochemistry
Cell
Transforming Growth Factor beta1
Myosin-Light-Chain Phosphatase
03 medical and health sciences
medicine
Humans
Calcium Signaling
Smad3 Protein
Phosphorylation
Molecular Biology
Rho-associated protein kinase
Cells
Cultured

Excitation Contraction Coupling
Calcium signaling
rho-Associated Kinases
business.industry
Muscle
Smooth

Cell Biology
respiratory system
Asthma
respiratory tract diseases
Cell biology
030104 developmental biology
medicine.anatomical_structure
Cytokine
Immunology
Myosin-light-chain phosphatase
Bronchial Hyperreactivity
medicine.symptom
rhoA GTP-Binding Protein
business
Transforming growth factor
Zdroj: American Journal of Respiratory Cell and Molecular Biology. 58:575-584
ISSN: 1535-4989
1044-1549
DOI: 10.1165/rcmb.2017-0247oc
Popis: Transforming growth factor β1 (TGF-β1), a cytokine whose levels are elevated in the airways of patients with asthma, perpetuates airway inflammation and modulates airway structural cell remodeling. However, the role of TGF-β1 in excessive airway narrowing in asthma, or airway hyperresponsiveness (AHR), remains unclear. In this study, we set out to investigate the direct effects of TGF-β1 on human airway smooth muscle (HASM) cell shortening and hyperresponsiveness. The dynamics of AHR and single-cell excitation-contraction coupling were measured in human precision-cut lung slices and in isolated HASM cells using supravital microscopy and magnetic twisting cytometry, respectively. In human precision-cut lung slices, overnight treatment with TGF-β1 significantly augmented basal and carbachol-induced bronchoconstriction. In isolated HASM cells, TGF-β1 increased basal and methacholine-induced cytoskeletal stiffness in a dose- and time-dependent manner. TGF-β1-induced single-cell contraction was corroborated by concomitant increases in myosin light chain and myosin phosphatase target subunit 1 phosphorylation levels, which were attenuated by small interfering RNA-mediated knockdown of Smad3 and pharmacological inhibition of Rho kinase. Strikingly, these physiological effects of TGF-β1 occurred through a RhoA-independent mechanism, with little effect on HASM cell [Ca2+]i levels. Together, our data suggest that TGF-β1 enhances HASM excitation-contraction coupling pathways to induce HASM cell shortening and hyperresponsiveness. These findings reveal a potential link between airway injury-repair responses and bronchial hyperreactivity in asthma, and define TGF-β1 signaling as a potential target to reduce AHR in asthma.
Databáze: OpenAIRE