» Articles » PMID: 36796098

Membrane Adhesion Junctions Regulate Airway Smooth Muscle Phenotype and Function

Overview
Journal Physiol Rev
Specialty Physiology
Date 2023 Feb 16
PMID 36796098
Authors
Affiliations
Soon will be listed here.
Abstract

The local environment surrounding airway smooth muscle (ASM) cells has profound effects on the physiological and phenotypic properties of ASM tissues. ASM is continually subjected to the mechanical forces generated during breathing and to the constituents of its surrounding extracellular milieu. The smooth muscle cells within the airways continually modulate their properties to adapt to these changing environmental influences. Smooth muscle cells connect to the extracellular cell matrix (ECM) at membrane adhesion junctions that provide mechanical coupling between smooth muscle cells within the tissue. Membrane adhesion junctions also sense local environmental signals and transduce them to cytoplasmic and nuclear signaling pathways in the ASM cell. Adhesion junctions are composed of clusters of transmembrane integrin proteins that bind to ECM proteins outside the cell and to large multiprotein complexes in the submembranous cytoplasm. Physiological conditions and stimuli from the surrounding ECM are sensed by integrin proteins and transduced by submembranous adhesion complexes to signaling pathways to the cytoskeleton and nucleus. The transmission of information between the local environment of the cells and intracellular processes enables ASM cells to rapidly adapt their physiological properties to modulating influences in their extracellular environment: mechanical and physical forces that impinge on the cell, ECM constituents, local mediators, and metabolites. The structure and molecular organization of adhesion junction complexes and the actin cytoskeleton are dynamic and constantly changing in response to environmental influences. The ability of ASM to rapidly accommodate to the ever-changing conditions and fluctuating physical forces within its local environment is essential for its normal physiological function.

Citing Articles

Targeting cytoskeletal biomechanics to modulate airway smooth muscle contraction in asthma.

McCullough M, Joshi I, Pereira N, Fuentes N, Krishnan R, Druey K J Biol Chem. 2024; 301(1):108028.

PMID: 39615690 PMC: 11721269. DOI: 10.1016/j.jbc.2024.108028.


N-cadherin antagonism is bronchoprotective in severe asthma models.

Pereira N, Schaible N, Desai A, Chan E, Ablooglu A, Capuano J Sci Adv. 2024; 10(48):eadp8872.

PMID: 39612338 PMC: 11606448. DOI: 10.1126/sciadv.adp8872.


Focal adhesion kinase activation is involved in contractile stimulation-induced detrusor muscle contraction in mice.

Maher S, Bayachou M, Fu P, Hijaz A, Liu G Eur J Pharmacol. 2023; 952:175807.

PMID: 37236435 PMC: 10330804. DOI: 10.1016/j.ejphar.2023.175807.

References
1.
Franco S, Rodgers M, Perrin B, Han J, Bennin D, Critchley D . Calpain-mediated proteolysis of talin regulates adhesion dynamics. Nat Cell Biol. 2004; 6(10):977-83. DOI: 10.1038/ncb1175. View

2.
Hirshman C, Zhu D, Pertel T, Panettieri R, Emala C . Isoproterenol induces actin depolymerization in human airway smooth muscle cells via activation of an Src kinase and GS. Am J Physiol Lung Cell Mol Physiol. 2005; 288(5):L924-31. DOI: 10.1152/ajplung.00463.2004. View

3.
Huang Y, J Gunst S . Phenotype transitions induced by mechanical stimuli in airway smooth muscle are regulated by differential interactions of parvin isoforms with paxillin and Akt. Am J Physiol Lung Cell Mol Physiol. 2020; 318(5):L1036-L1055. PMC: 7272735. DOI: 10.1152/ajplung.00506.2019. View

4.
Fukuda T, Guo L, Shi X, Wu C . CH-ILKBP regulates cell survival by facilitating the membrane translocation of protein kinase B/Akt. J Cell Biol. 2003; 160(7):1001-8. PMC: 2172761. DOI: 10.1083/jcb.200212113. View

5.
Togashi H, Emala C, Hall I, Hirshman C . Carbachol-induced actin reorganization involves Gi activation of Rho in human airway smooth muscle cells. Am J Physiol. 1998; 274(5):L803-9. DOI: 10.1152/ajplung.1998.274.5.L803. View