Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices

Author:

Ram-Mohan Sumati1,Bai Yan2,Schaible Niccole1,Ehrlicher Allen J.3,Cook Daniel P.4,Suki Bela5ORCID,Stoltz David A.4,Solway Julian6,Ai Xingbin2,Krishnan Ramaswamy1

Affiliation:

1. Center for Vascular Biology Research, Department of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts

2. Pulmonary and Critical Care Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts

3. Department of Bioengineering, McGill University, Montreal, Quebec, Canada

4. Department of Internal Medicine, University of Iowa, Iowa City, Iowa

5. Biomedical Engineering Department, Boston University, Boston, Massachusetts

6. Department of Medicine, University of Chicago, Chicago, Illinois

Abstract

In asthma, acute bronchospasm is driven by contractile forces of airway smooth muscle (ASM). These forces can be imaged in the cultured ASM cell or assessed in the muscle strip and the tracheal/bronchial ring, but in each case, the ASM is studied in isolation from the native airway milieu. Here, we introduce a novel platform called tissue traction microscopy (TTM) to measure ASM contractile force within porcine and human precision-cut lung slices (PCLS). Compared with the conventional measurements of lumen area changes in PCLS, TTM measurements of ASM force changes are 1) more sensitive to bronchoconstrictor stimuli, 2) less variable across airways, and 3) provide spatial information. Notably, within every human airway, TTM measurements revealed local regions of high ASM contraction that we call “stress hotspots”. As an acute response to cyclic stretch, these hotspots promptly decreased but eventually recovered in magnitude, spatial location, and orientation, consistent with local ASM fluidization and resolidification. By enabling direct and precise measurements of ASM force, TTM should accelerate preclinical studies of airway reactivity.

Funder

National Institutes of Health

Cystic Fibrosis Foundation

NSERC RGPIN

EQPEQ

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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