Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells. Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated...
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Veröffentlicht in: | Journal of leukocyte biology 2009-11, Vol.86 (5), p.1145-1151 |
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description | Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells.
Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune‐mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung. |
doi_str_mv | 10.1189/jlb.0209078 |
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Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune‐mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung.</description><identifier>ISSN: 0741-5400</identifier><identifier>EISSN: 1938-3673</identifier><identifier>DOI: 10.1189/jlb.0209078</identifier><identifier>PMID: 19638499</identifier><language>eng</language><publisher>England: Society for Leukocyte Biology</publisher><subject>Animals ; Cell Differentiation ; Chemokines, CXC - physiology ; Coronavirus - isolation & purification ; Coronavirus - physiology ; Coronavirus Infections - immunology ; Coronavirus Infections - physiopathology ; CXC chemokine ; Epithelial Cells - immunology ; Epithelial Cells - pathology ; Epithelial Cells - physiology ; Epithelial Cells - virology ; Host-Pathogen Interactions - physiology ; Humans ; innate immunity ; Lung - virology ; Lung Diseases - virology ; lung infection ; Mini‐Review ; Mini‐Reviews ; neutrophil recruitment ; pneumocyte ; Pulmonary Alveoli - immunology ; Pulmonary Alveoli - physiopathology ; Pulmonary Alveoli - virology ; Rats ; Respiratory Tract Infections - epidemiology ; Respiratory Tract Infections - virology ; SARS ; Severe Acute Respiratory Syndrome - immunology ; Severe Acute Respiratory Syndrome - physiopathology ; Severe acute respiratory syndrome-related coronavirus - physiology ; Virus Diseases - epidemiology ; Virus Diseases - immunology</subject><ispartof>Journal of leukocyte biology, 2009-11, Vol.86 (5), p.1145-1151</ispartof><rights>2009 Society for Leukocyte Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4525-e8a4ba3061c5c989d96ebc2a4b8587d3e80e8f35353391214fb4f5163624af953</citedby><cites>FETCH-LOGICAL-c4525-e8a4ba3061c5c989d96ebc2a4b8587d3e80e8f35353391214fb4f5163624af953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1189%2Fjlb.0209078$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1189%2Fjlb.0209078$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19638499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miura, Tanya A.</creatorcontrib><creatorcontrib>Holmes, Kathryn V.</creatorcontrib><title>Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells</title><title>Journal of leukocyte biology</title><addtitle>J Leukoc Biol</addtitle><description>Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells.
Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune‐mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung.</description><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Chemokines, CXC - physiology</subject><subject>Coronavirus - isolation & purification</subject><subject>Coronavirus - physiology</subject><subject>Coronavirus Infections - immunology</subject><subject>Coronavirus Infections - physiopathology</subject><subject>CXC chemokine</subject><subject>Epithelial Cells - immunology</subject><subject>Epithelial Cells - pathology</subject><subject>Epithelial Cells - physiology</subject><subject>Epithelial Cells - virology</subject><subject>Host-Pathogen Interactions - physiology</subject><subject>Humans</subject><subject>innate immunity</subject><subject>Lung - virology</subject><subject>Lung Diseases - virology</subject><subject>lung infection</subject><subject>Mini‐Review</subject><subject>Mini‐Reviews</subject><subject>neutrophil recruitment</subject><subject>pneumocyte</subject><subject>Pulmonary Alveoli - immunology</subject><subject>Pulmonary Alveoli - physiopathology</subject><subject>Pulmonary Alveoli - virology</subject><subject>Rats</subject><subject>Respiratory Tract Infections - epidemiology</subject><subject>Respiratory Tract Infections - virology</subject><subject>SARS</subject><subject>Severe Acute Respiratory Syndrome - immunology</subject><subject>Severe Acute Respiratory Syndrome - physiopathology</subject><subject>Severe acute respiratory syndrome-related coronavirus - physiology</subject><subject>Virus Diseases - epidemiology</subject><subject>Virus Diseases - immunology</subject><issn>0741-5400</issn><issn>1938-3673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFP5CAYxcnGjY66p72bnvRgqlCghYuJGnXWTOJFb5sQynydYpgyQjuN_72dmcZdL4YDCe_H-x48hH4TfEGIkJevrrzAGZa4ED_QhEgqUpoXdA9NcMFIyhnGB-gwxleMMc1yvI8OiMypYFJO0N-pj2260m3tF9AktmkhaNNa38Rk3gXbLBLjg2_02oYuDnoFWzXxVbIKdqnDe6LdGrzTIYGVbWtwVrvEgHPxGP2stIvwa9yP0Mv93fPtNJ09Pfy5vZ6lhvGMpyA0KzXFOTHcSCHnMofSZMOh4KKYUxAYREX5sKgkGWFVySpOcppnTFeS0yN0tfNddeUS5gaaNminxnzKa6u-Ko2t1cKvVVYUTIiNwdloEPxbB7FVSxs3T9AN-C6qgjJCOCdsIM93pAk-xgDV5xSC1aYONdShxjoG-uT_YP_Y8f8HAO-A3jp4_85LPc5uCGGbrKe7K7Vd1L0NoOJSOzdMyFTf9yJXXG3BD6H6pKM</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Miura, Tanya A.</creator><creator>Holmes, Kathryn V.</creator><general>Society for Leukocyte Biology</general><general>John Wiley and Sons Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>200911</creationdate><title>Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells</title><author>Miura, Tanya A. ; Holmes, Kathryn V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4525-e8a4ba3061c5c989d96ebc2a4b8587d3e80e8f35353391214fb4f5163624af953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cell Differentiation</topic><topic>Chemokines, CXC - physiology</topic><topic>Coronavirus - isolation & purification</topic><topic>Coronavirus - physiology</topic><topic>Coronavirus Infections - immunology</topic><topic>Coronavirus Infections - physiopathology</topic><topic>CXC chemokine</topic><topic>Epithelial Cells - immunology</topic><topic>Epithelial Cells - pathology</topic><topic>Epithelial Cells - physiology</topic><topic>Epithelial Cells - virology</topic><topic>Host-Pathogen Interactions - physiology</topic><topic>Humans</topic><topic>innate immunity</topic><topic>Lung - virology</topic><topic>Lung Diseases - virology</topic><topic>lung infection</topic><topic>Mini‐Review</topic><topic>Mini‐Reviews</topic><topic>neutrophil recruitment</topic><topic>pneumocyte</topic><topic>Pulmonary Alveoli - immunology</topic><topic>Pulmonary Alveoli - physiopathology</topic><topic>Pulmonary Alveoli - virology</topic><topic>Rats</topic><topic>Respiratory Tract Infections - epidemiology</topic><topic>Respiratory Tract Infections - virology</topic><topic>SARS</topic><topic>Severe Acute Respiratory Syndrome - immunology</topic><topic>Severe Acute Respiratory Syndrome - physiopathology</topic><topic>Severe acute respiratory syndrome-related coronavirus - physiology</topic><topic>Virus Diseases - epidemiology</topic><topic>Virus Diseases - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miura, Tanya A.</creatorcontrib><creatorcontrib>Holmes, Kathryn V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of leukocyte biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miura, Tanya A.</au><au>Holmes, Kathryn V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells</atitle><jtitle>Journal of leukocyte biology</jtitle><addtitle>J Leukoc Biol</addtitle><date>2009-11</date><risdate>2009</risdate><volume>86</volume><issue>5</issue><spage>1145</spage><epage>1151</epage><pages>1145-1151</pages><issn>0741-5400</issn><eissn>1938-3673</eissn><abstract>Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells.
Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune‐mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung.</abstract><cop>England</cop><pub>Society for Leukocyte Biology</pub><pmid>19638499</pmid><doi>10.1189/jlb.0209078</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Differentiation Chemokines, CXC - physiology Coronavirus - isolation & purification Coronavirus - physiology Coronavirus Infections - immunology Coronavirus Infections - physiopathology CXC chemokine Epithelial Cells - immunology Epithelial Cells - pathology Epithelial Cells - physiology Epithelial Cells - virology Host-Pathogen Interactions - physiology Humans innate immunity Lung - virology Lung Diseases - virology lung infection Mini‐Review Mini‐Reviews neutrophil recruitment pneumocyte Pulmonary Alveoli - immunology Pulmonary Alveoli - physiopathology Pulmonary Alveoli - virology Rats Respiratory Tract Infections - epidemiology Respiratory Tract Infections - virology SARS Severe Acute Respiratory Syndrome - immunology Severe Acute Respiratory Syndrome - physiopathology Severe acute respiratory syndrome-related coronavirus - physiology Virus Diseases - epidemiology Virus Diseases - immunology |
title | Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells |
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