Formaldehyde Induces Rho-Associated Kinase Activity to Evoke Airway Hyperresponsiveness
Formaldehyde, a common indoor air pollutant, exacerbates asthma and synergizes with allergen to induce airway hyperresponsiveness (AHR) in animal models. The mechanisms mediating formaldehyde-induced AHR remain poorly understood. We posit that formaldehyde modulates agonist-induced contractile respo...
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creator | Jude, Joseph Koziol-White, Cynthia Scala, Jacqueline Yoo, Edwin Jester, William Maute, Christopher Dalton, Pamela Panettieri, Jr, Reynold |
description | Formaldehyde, a common indoor air pollutant, exacerbates asthma and synergizes with allergen to induce airway hyperresponsiveness (AHR) in animal models. The mechanisms mediating formaldehyde-induced AHR remain poorly understood. We posit that formaldehyde modulates agonist-induced contractile response of human airway smooth muscle (HASM) cells to elicit AHR. HASM cells were exposed to formaldehyde or vehicle and agonist-induced intracellular Ca
([Ca
]
) and myosin light-chain phosphatase (MYPT1) phosphorylation were determined. Air-liquid interface-differentiated human bronchial epithelial (HBE) cells were exposed to formaldehyde or vehicle and cocultured with HASM cells. Agonist-induced [Ca
]
and MYPT1 phosphorylation were determined in the cocultured HASM cells. Precision-cut human lung slices were exposed to PBS or varying concentrations of formaldehyde, and then carbachol-induced airway narrowing was determined 24 hours after exposure. HASM cells were transfected with nontargeting or nuclear factor erythroid-derived 2, like 2 (Nrf-2)-targeting small interfering RNA and exposed to formaldehyde or vehicle, followed by determination of antioxidant response (quinone oxido-reductase 1 and thioredoxin 1) and basal and agonist-induced MYPT1 phosphorylation. Formaldehyde enhanced the basal Rho-kinase activity and MYPT1 phosphorylation with little effect on agonist-induced [Ca
]
in HASM cells. Formaldehyde induced Nrf-2-dependent antioxidant response in HASM cells, although the MYPT1 phosphorylation was independent of Nrf-2 induction. Although HBE cells exposed to formaldehyde had little effect on agonist-induced [Ca
]
or MYPT1 phosphorylation in cocultured HASM cells, formaldehyde enhanced carbachol-induced airway responsiveness in precision-cut human lung slices. In conclusion, formaldehyde induces phosphorylation of the regulatory subunit of MYPT1, independent of formaldehyde-induced Nrf-2 activation in HASM cells. The findings suggest that the Rho kinase-dependent Ca
sensitization pathway plays a role in formaldehyde-induced AHR. |
doi_str_mv | 10.1165/rcmb.2015-0254OC |
format | Article |
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([Ca
]
) and myosin light-chain phosphatase (MYPT1) phosphorylation were determined. Air-liquid interface-differentiated human bronchial epithelial (HBE) cells were exposed to formaldehyde or vehicle and cocultured with HASM cells. Agonist-induced [Ca
]
and MYPT1 phosphorylation were determined in the cocultured HASM cells. Precision-cut human lung slices were exposed to PBS or varying concentrations of formaldehyde, and then carbachol-induced airway narrowing was determined 24 hours after exposure. HASM cells were transfected with nontargeting or nuclear factor erythroid-derived 2, like 2 (Nrf-2)-targeting small interfering RNA and exposed to formaldehyde or vehicle, followed by determination of antioxidant response (quinone oxido-reductase 1 and thioredoxin 1) and basal and agonist-induced MYPT1 phosphorylation. Formaldehyde enhanced the basal Rho-kinase activity and MYPT1 phosphorylation with little effect on agonist-induced [Ca
]
in HASM cells. Formaldehyde induced Nrf-2-dependent antioxidant response in HASM cells, although the MYPT1 phosphorylation was independent of Nrf-2 induction. Although HBE cells exposed to formaldehyde had little effect on agonist-induced [Ca
]
or MYPT1 phosphorylation in cocultured HASM cells, formaldehyde enhanced carbachol-induced airway responsiveness in precision-cut human lung slices. In conclusion, formaldehyde induces phosphorylation of the regulatory subunit of MYPT1, independent of formaldehyde-induced Nrf-2 activation in HASM cells. The findings suggest that the Rho kinase-dependent Ca
sensitization pathway plays a role in formaldehyde-induced AHR.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/rcmb.2015-0254OC</identifier><identifier>PMID: 27149505</identifier><language>eng</language><publisher>United States: American Thoracic Society</publisher><subject>Air pollution ; Aldehydes ; Asthma ; Gene expression ; Homeostasis ; Inflammation ; Kinases ; Occupational safety ; Original Research ; Phosphatase ; Phosphorylation ; Pollutants ; Proteins ; Smooth muscle ; Studies</subject><ispartof>American journal of respiratory cell and molecular biology, 2016-10, Vol.55 (4), p.542-553</ispartof><rights>Copyright American Thoracic Society Oct 2016</rights><rights>Copyright © 2016 by the American Thoracic Society 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-7e53b2c27f3f1b42ce535de5dd3b37df4a80b786912db1fca9c0e0790660fdd53</citedby><cites>FETCH-LOGICAL-c457t-7e53b2c27f3f1b42ce535de5dd3b37df4a80b786912db1fca9c0e0790660fdd53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27149505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jude, Joseph</creatorcontrib><creatorcontrib>Koziol-White, Cynthia</creatorcontrib><creatorcontrib>Scala, Jacqueline</creatorcontrib><creatorcontrib>Yoo, Edwin</creatorcontrib><creatorcontrib>Jester, William</creatorcontrib><creatorcontrib>Maute, Christopher</creatorcontrib><creatorcontrib>Dalton, Pamela</creatorcontrib><creatorcontrib>Panettieri, Jr, Reynold</creatorcontrib><title>Formaldehyde Induces Rho-Associated Kinase Activity to Evoke Airway Hyperresponsiveness</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>Formaldehyde, a common indoor air pollutant, exacerbates asthma and synergizes with allergen to induce airway hyperresponsiveness (AHR) in animal models. The mechanisms mediating formaldehyde-induced AHR remain poorly understood. We posit that formaldehyde modulates agonist-induced contractile response of human airway smooth muscle (HASM) cells to elicit AHR. HASM cells were exposed to formaldehyde or vehicle and agonist-induced intracellular Ca
([Ca
]
) and myosin light-chain phosphatase (MYPT1) phosphorylation were determined. Air-liquid interface-differentiated human bronchial epithelial (HBE) cells were exposed to formaldehyde or vehicle and cocultured with HASM cells. Agonist-induced [Ca
]
and MYPT1 phosphorylation were determined in the cocultured HASM cells. Precision-cut human lung slices were exposed to PBS or varying concentrations of formaldehyde, and then carbachol-induced airway narrowing was determined 24 hours after exposure. HASM cells were transfected with nontargeting or nuclear factor erythroid-derived 2, like 2 (Nrf-2)-targeting small interfering RNA and exposed to formaldehyde or vehicle, followed by determination of antioxidant response (quinone oxido-reductase 1 and thioredoxin 1) and basal and agonist-induced MYPT1 phosphorylation. Formaldehyde enhanced the basal Rho-kinase activity and MYPT1 phosphorylation with little effect on agonist-induced [Ca
]
in HASM cells. Formaldehyde induced Nrf-2-dependent antioxidant response in HASM cells, although the MYPT1 phosphorylation was independent of Nrf-2 induction. Although HBE cells exposed to formaldehyde had little effect on agonist-induced [Ca
]
or MYPT1 phosphorylation in cocultured HASM cells, formaldehyde enhanced carbachol-induced airway responsiveness in precision-cut human lung slices. In conclusion, formaldehyde induces phosphorylation of the regulatory subunit of MYPT1, independent of formaldehyde-induced Nrf-2 activation in HASM cells. The findings suggest that the Rho kinase-dependent Ca
sensitization pathway plays a role in formaldehyde-induced AHR.</description><subject>Air pollution</subject><subject>Aldehydes</subject><subject>Asthma</subject><subject>Gene expression</subject><subject>Homeostasis</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Occupational safety</subject><subject>Original Research</subject><subject>Phosphatase</subject><subject>Phosphorylation</subject><subject>Pollutants</subject><subject>Proteins</subject><subject>Smooth muscle</subject><subject>Studies</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkU1v1DAQhi0EoqVw54QiceklZez4I74grVYtrahUCYE4Wo49YV2SeLGTRfn3JNpSASdO_nrm1YwfQl5TuKBUinfJ9c0FAypKYILfbZ-QUyoqUXJd66fLHjgvqeD6hLzI-R6AsprS5-SEKcq1AHFKvl7F1NvO4272WNwMfnKYi0-7WG5yji7YEX3xMQw2Y7FxYziEcS7GWFwe4vflJqSfdi6u5z2mhHkfhxwOOGDOL8mz1nYZXz2sZ-TL1eXn7XV5e_fhZru5LR0XaiwViqphjqm2amnDmVvOwqPwvmoq5Vtua2hULTVlvqGts9oBgtIgJbTei-qMvD_m7qemR-9wGJPtzD6F3qbZRBvM3y9D2Jlv8WAEKKDAloDzh4AUf0yYR9OH7LDr7IBxyobWlWJaMqH-A2VSKi3lmvr2H_Q-TmlYfmKlNDC1TLBQcKRcijknbB_7pmBWwWYVbFbB5ih4KXnz57yPBb-NVr8A3Xqjdg</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Jude, Joseph</creator><creator>Koziol-White, Cynthia</creator><creator>Scala, Jacqueline</creator><creator>Yoo, Edwin</creator><creator>Jester, William</creator><creator>Maute, Christopher</creator><creator>Dalton, Pamela</creator><creator>Panettieri, Jr, Reynold</creator><general>American Thoracic Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>7TV</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>201610</creationdate><title>Formaldehyde Induces Rho-Associated Kinase Activity to Evoke Airway Hyperresponsiveness</title><author>Jude, Joseph ; 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The mechanisms mediating formaldehyde-induced AHR remain poorly understood. We posit that formaldehyde modulates agonist-induced contractile response of human airway smooth muscle (HASM) cells to elicit AHR. HASM cells were exposed to formaldehyde or vehicle and agonist-induced intracellular Ca
([Ca
]
) and myosin light-chain phosphatase (MYPT1) phosphorylation were determined. Air-liquid interface-differentiated human bronchial epithelial (HBE) cells were exposed to formaldehyde or vehicle and cocultured with HASM cells. Agonist-induced [Ca
]
and MYPT1 phosphorylation were determined in the cocultured HASM cells. Precision-cut human lung slices were exposed to PBS or varying concentrations of formaldehyde, and then carbachol-induced airway narrowing was determined 24 hours after exposure. HASM cells were transfected with nontargeting or nuclear factor erythroid-derived 2, like 2 (Nrf-2)-targeting small interfering RNA and exposed to formaldehyde or vehicle, followed by determination of antioxidant response (quinone oxido-reductase 1 and thioredoxin 1) and basal and agonist-induced MYPT1 phosphorylation. Formaldehyde enhanced the basal Rho-kinase activity and MYPT1 phosphorylation with little effect on agonist-induced [Ca
]
in HASM cells. Formaldehyde induced Nrf-2-dependent antioxidant response in HASM cells, although the MYPT1 phosphorylation was independent of Nrf-2 induction. Although HBE cells exposed to formaldehyde had little effect on agonist-induced [Ca
]
or MYPT1 phosphorylation in cocultured HASM cells, formaldehyde enhanced carbachol-induced airway responsiveness in precision-cut human lung slices. In conclusion, formaldehyde induces phosphorylation of the regulatory subunit of MYPT1, independent of formaldehyde-induced Nrf-2 activation in HASM cells. The findings suggest that the Rho kinase-dependent Ca
sensitization pathway plays a role in formaldehyde-induced AHR.</abstract><cop>United States</cop><pub>American Thoracic Society</pub><pmid>27149505</pmid><doi>10.1165/rcmb.2015-0254OC</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Air pollution Aldehydes Asthma Gene expression Homeostasis Inflammation Kinases Occupational safety Original Research Phosphatase Phosphorylation Pollutants Proteins Smooth muscle Studies |
title | Formaldehyde Induces Rho-Associated Kinase Activity to Evoke Airway Hyperresponsiveness |
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