Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices
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...
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Veröffentlicht in: | American journal of physiology. Lung cellular and molecular physiology 2020-02, Vol.318 (2), p.L323-L330 |
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container_title | American journal of physiology. Lung cellular and molecular physiology |
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creator | Ram-Mohan, Sumati Bai, Yan Schaible, Niccole Ehrlicher, Allen J Cook, Daniel P Suki, Bela Stoltz, David A Solway, Julian Ai, Xingbin Krishnan, Ramaswamy |
description | 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
) more sensitive to bronchoconstrictor stimuli,
) less variable across airways, and
) 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. |
doi_str_mv | 10.1152/ajplung.00297.2019 |
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) more sensitive to bronchoconstrictor stimuli,
) less variable across airways, and
) 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.</description><identifier>ISSN: 1040-0605</identifier><identifier>ISSN: 1522-1504</identifier><identifier>EISSN: 1522-1504</identifier><identifier>DOI: 10.1152/ajplung.00297.2019</identifier><identifier>PMID: 31774304</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Animals, Newborn ; Asthma ; Biomechanical Phenomena ; Bronchoconstriction - physiology ; Bronchospasm ; Fluidization ; Fluidizing ; Humans ; Innovative Methodology ; Lung - physiology ; Lungs ; Microscopy ; Muscle contraction ; Muscle Contraction - physiology ; Muscle, Smooth - physiology ; Muscles ; Muscular function ; Respiratory tract ; Smooth muscle ; Spatial data ; Stress, Mechanical ; Swine ; Traction</subject><ispartof>American journal of physiology. Lung cellular and molecular physiology, 2020-02, Vol.318 (2), p.L323-L330</ispartof><rights>Copyright American Physiological Society Feb 2020</rights><rights>Copyright © 2020 the American Physiological Society 2020 American Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-3d31120cd7483c3b07c3e761bf48fe554aa9c15a64a104ab89e72a6f5c23d6c83</citedby><cites>FETCH-LOGICAL-c430t-3d31120cd7483c3b07c3e761bf48fe554aa9c15a64a104ab89e72a6f5c23d6c83</cites><orcidid>0000-0002-9720-1006</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31774304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ram-Mohan, Sumati</creatorcontrib><creatorcontrib>Bai, Yan</creatorcontrib><creatorcontrib>Schaible, Niccole</creatorcontrib><creatorcontrib>Ehrlicher, Allen J</creatorcontrib><creatorcontrib>Cook, Daniel P</creatorcontrib><creatorcontrib>Suki, Bela</creatorcontrib><creatorcontrib>Stoltz, David A</creatorcontrib><creatorcontrib>Solway, Julian</creatorcontrib><creatorcontrib>Ai, Xingbin</creatorcontrib><creatorcontrib>Krishnan, Ramaswamy</creatorcontrib><title>Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices</title><title>American journal of physiology. Lung cellular and molecular physiology</title><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><description>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
) more sensitive to bronchoconstrictor stimuli,
) less variable across airways, and
) 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.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Asthma</subject><subject>Biomechanical Phenomena</subject><subject>Bronchoconstriction - physiology</subject><subject>Bronchospasm</subject><subject>Fluidization</subject><subject>Fluidizing</subject><subject>Humans</subject><subject>Innovative Methodology</subject><subject>Lung - physiology</subject><subject>Lungs</subject><subject>Microscopy</subject><subject>Muscle contraction</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle, Smooth - physiology</subject><subject>Muscles</subject><subject>Muscular function</subject><subject>Respiratory tract</subject><subject>Smooth muscle</subject><subject>Spatial data</subject><subject>Stress, Mechanical</subject><subject>Swine</subject><subject>Traction</subject><issn>1040-0605</issn><issn>1522-1504</issn><issn>1522-1504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1O3DAUha0KVOi0L9AFssSmmwzXf3GyQapQKZWQ2AwbNpbnjgMeJXGI41bz9jgwHbWsbPl-9-gcH0K-MlgypviF3Q5t6h-XALzWSw6s_kBO84AXTIE8yneQUEAJ6oR8inELAAqg_EhOBNNaCpCn5GHlY0yOTqPFyYeedh7HEDEMOzoF-pxsP_lmR7sUsXUUQ38g__jpyfd0GB36mB8KTBOdDdHYenTxMzlubBvdl_25IPfXP1ZXN8Xt3c9fV99vC8wWpkJsBGMccKNlJVCsQaNwumTrRlaNU0paWyNTtpQ257Hrqnaa27JRyMWmxEosyOWb7pDWndugmy22Zhh9Z8edCdab_ye9fzKP4bfRoHhZiSzwbS8whufk4mQ6H9G1re1dSNFwwWpWa64go-fv0G1IY5_jZUoqxWou6kzxN2r-yji65mCGgZmrM_vqzGt1Zq4uL539G-Ow8rcr8QLV-5jV</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Ram-Mohan, Sumati</creator><creator>Bai, Yan</creator><creator>Schaible, Niccole</creator><creator>Ehrlicher, Allen J</creator><creator>Cook, Daniel P</creator><creator>Suki, Bela</creator><creator>Stoltz, David A</creator><creator>Solway, Julian</creator><creator>Ai, Xingbin</creator><creator>Krishnan, Ramaswamy</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9720-1006</orcidid></search><sort><creationdate>20200201</creationdate><title>Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices</title><author>Ram-Mohan, Sumati ; Bai, Yan ; Schaible, Niccole ; Ehrlicher, Allen J ; Cook, Daniel P ; Suki, Bela ; Stoltz, David A ; Solway, Julian ; Ai, Xingbin ; Krishnan, Ramaswamy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-3d31120cd7483c3b07c3e761bf48fe554aa9c15a64a104ab89e72a6f5c23d6c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Asthma</topic><topic>Biomechanical Phenomena</topic><topic>Bronchoconstriction - physiology</topic><topic>Bronchospasm</topic><topic>Fluidization</topic><topic>Fluidizing</topic><topic>Humans</topic><topic>Innovative Methodology</topic><topic>Lung - physiology</topic><topic>Lungs</topic><topic>Microscopy</topic><topic>Muscle contraction</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle, Smooth - physiology</topic><topic>Muscles</topic><topic>Muscular function</topic><topic>Respiratory tract</topic><topic>Smooth muscle</topic><topic>Spatial data</topic><topic>Stress, Mechanical</topic><topic>Swine</topic><topic>Traction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ram-Mohan, Sumati</creatorcontrib><creatorcontrib>Bai, Yan</creatorcontrib><creatorcontrib>Schaible, Niccole</creatorcontrib><creatorcontrib>Ehrlicher, Allen J</creatorcontrib><creatorcontrib>Cook, Daniel P</creatorcontrib><creatorcontrib>Suki, Bela</creatorcontrib><creatorcontrib>Stoltz, David A</creatorcontrib><creatorcontrib>Solway, Julian</creatorcontrib><creatorcontrib>Ai, Xingbin</creatorcontrib><creatorcontrib>Krishnan, Ramaswamy</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ram-Mohan, Sumati</au><au>Bai, Yan</au><au>Schaible, Niccole</au><au>Ehrlicher, Allen J</au><au>Cook, Daniel P</au><au>Suki, Bela</au><au>Stoltz, David A</au><au>Solway, Julian</au><au>Ai, Xingbin</au><au>Krishnan, Ramaswamy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>318</volume><issue>2</issue><spage>L323</spage><epage>L330</epage><pages>L323-L330</pages><issn>1040-0605</issn><issn>1522-1504</issn><eissn>1522-1504</eissn><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
) more sensitive to bronchoconstrictor stimuli,
) less variable across airways, and
) 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.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>31774304</pmid><doi>10.1152/ajplung.00297.2019</doi><orcidid>https://orcid.org/0000-0002-9720-1006</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Newborn Asthma Biomechanical Phenomena Bronchoconstriction - physiology Bronchospasm Fluidization Fluidizing Humans Innovative Methodology Lung - physiology Lungs Microscopy Muscle contraction Muscle Contraction - physiology Muscle, Smooth - physiology Muscles Muscular function Respiratory tract Smooth muscle Spatial data Stress, Mechanical Swine Traction |
title | Tissue traction microscopy to quantify muscle contraction within precision-cut lung slices |
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