Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells.
Identifieur interne : 001856 ( PubMed/Curation ); précédent : 001855; suivant : 001857Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells.
Auteurs : Tanya A. Miura [États-Unis] ; Kathryn V. HolmesSource :
- Journal of leukocyte biology [ 1938-3673 ] ; 2009.
Descripteurs français
- KwdFr :
- Alvéoles pulmonaires (immunologie), Alvéoles pulmonaires (physiopathologie), Alvéoles pulmonaires (virologie), Animaux, Cellules épithéliales (anatomopathologie), Cellules épithéliales (immunologie), Cellules épithéliales (physiologie), Cellules épithéliales (virologie), Chimiokines CXC (physiologie), Coronavirus (isolement et purification), Coronavirus (physiologie), Différenciation cellulaire, Humains, Infections de l'appareil respiratoire (virologie), Infections de l'appareil respiratoire (épidémiologie), Infections à coronavirus (immunologie), Infections à coronavirus (physiopathologie), Interactions hôte-pathogène (physiologie), Maladies pulmonaires (virologie), Maladies virales (immunologie), Maladies virales (épidémiologie), Poumon (virologie), Rats, Syndrome respiratoire aigu sévère (immunologie), Syndrome respiratoire aigu sévère (physiopathologie), Virus du SRAS (physiologie).
- MESH :
- anatomopathologie : Cellules épithéliales.
- immunologie : Alvéoles pulmonaires, Cellules épithéliales, Infections à coronavirus, Maladies virales, Syndrome respiratoire aigu sévère.
- isolement et purification : Coronavirus.
- physiologie : Cellules épithéliales, Chimiokines CXC, Coronavirus, Interactions hôte-pathogène, Virus du SRAS.
- physiopathologie : Alvéoles pulmonaires, Infections à coronavirus, Syndrome respiratoire aigu sévère.
- virologie : Alvéoles pulmonaires, Cellules épithéliales, Infections de l'appareil respiratoire, Maladies pulmonaires, Poumon.
- épidémiologie : Infections de l'appareil respiratoire, Maladies virales.
- Animaux, Différenciation cellulaire, Humains, Rats.
English descriptors
- KwdEn :
- Animals, Cell Differentiation, Chemokines, CXC (physiology), Coronavirus (isolation & purification), Coronavirus (physiology), Coronavirus Infections (immunology), Coronavirus Infections (physiopathology), Epithelial Cells (immunology), Epithelial Cells (pathology), Epithelial Cells (physiology), Epithelial Cells (virology), Host-Pathogen Interactions (physiology), Humans, Lung (virology), Lung Diseases (virology), Pulmonary Alveoli (immunology), Pulmonary Alveoli (physiopathology), Pulmonary Alveoli (virology), Rats, Respiratory Tract Infections (epidemiology), Respiratory Tract Infections (virology), SARS Virus (physiology), Severe Acute Respiratory Syndrome (immunology), Severe Acute Respiratory Syndrome (physiopathology), Virus Diseases (epidemiology), Virus Diseases (immunology).
- MESH :
- chemical , physiology : Chemokines, CXC.
- epidemiology : Respiratory Tract Infections, Virus Diseases.
- immunology : Coronavirus Infections, Epithelial Cells, Pulmonary Alveoli, Severe Acute Respiratory Syndrome, Virus Diseases.
- isolation & purification : Coronavirus.
- pathology : Epithelial Cells.
- physiology : Coronavirus, Epithelial Cells, Host-Pathogen Interactions, SARS Virus.
- physiopathology : Coronavirus Infections, Pulmonary Alveoli, Severe Acute Respiratory Syndrome.
- virology : Epithelial Cells, Lung, Lung Diseases, Pulmonary Alveoli, Respiratory Tract Infections.
- Animals, Cell Differentiation, Humans, Rats.
Abstract
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: 10.1189/jlb.0209078
PubMed: 19638499
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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.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19638499</PMID><DateCompleted><Year>2010</Year><Month>01</Month><Day>06</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1938-3673</ISSN><JournalIssue CitedMedium="Internet"><Volume>86</Volume><Issue>5</Issue><PubDate><Year>2009</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Journal of leukocyte biology</Title><ISOAbbreviation>J. Leukoc. Biol.</ISOAbbreviation></Journal><ArticleTitle>Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells.</ArticleTitle><Pagination><MedlinePgn>1145-51</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1189/jlb.0209078</ELocationID><Abstract><AbstractText>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.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Miura</LastName><ForeName>Tanya A</ForeName><Initials>TA</Initials><AffiliationInfo><Affiliation>Department of Microbiology, Molecular Biology, and Biochemistry, University of Idaho, Moscow, Idaho, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Holmes</LastName><ForeName>Kathryn V</ForeName><Initials>KV</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>AI-059576</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>AI-25231</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>P01 AI059576</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>P20 RR015587</GrantID><Acronym>RR</Acronym><Agency>NCRR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 AI025231</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2009</Year><Month>07</Month><Day>28</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Leukoc Biol</MedlineTA><NlmUniqueID>8405628</NlmUniqueID><ISSNLinking>0741-5400</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D019743">Chemokines, CXC</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002454" MajorTopicYN="N">Cell Differentiation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019743" MajorTopicYN="N">Chemokines, CXC</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017934" MajorTopicYN="N">Coronavirus</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018352" MajorTopicYN="N">Coronavirus Infections</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004847" MajorTopicYN="N">Epithelial Cells</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName><QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D054884" MajorTopicYN="N">Host-Pathogen Interactions</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008168" MajorTopicYN="N">Lung</DescriptorName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008171" MajorTopicYN="N">Lung Diseases</DescriptorName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011650" MajorTopicYN="N">Pulmonary Alveoli</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName><QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051381" MajorTopicYN="N">Rats</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012141" MajorTopicYN="N">Respiratory Tract Infections</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D045473" MajorTopicYN="N">SARS Virus</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D045169" MajorTopicYN="N">Severe Acute Respiratory 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