Altered Exosomal RNA Profiles in Bronchoalveolar Lavage from Lung Transplants with Acute Rejection
The mechanism by which acute allograft rejection leads to chronic rejection remains poorly understood despite its common occurrence. Exosomes, membrane vesicles released from cells within the lung allograft, contain a diverse array of biomolecules that closely reflect the biologic state of the cell...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 2015-12, Vol.192 (12), p.1490-1503 |
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creator | Gregson, Aric L Hoji, Aki Injean, Patil Poynter, Steven T Briones, Claudia Palchevskiy, Vyacheslav Weigt, S Sam Shino, Michael Y Derhovanessian, Ariss Sayah, David Saggar, Rajan Ross, David Ardehali, Abbas Lynch, 3rd, Joseph P Belperio, John A |
description | The mechanism by which acute allograft rejection leads to chronic rejection remains poorly understood despite its common occurrence. Exosomes, membrane vesicles released from cells within the lung allograft, contain a diverse array of biomolecules that closely reflect the biologic state of the cell and tissue from which they are released. Exosome transcriptomes may provide a better understanding of the rejection process. Furthermore, biomarkers originating from this transcriptome could provide timely and sensitive detection of acute cellular rejection (AR), reducing the incidence of severe AR and chronic lung allograft dysfunction and improving outcomes.
To provide an in-depth analysis of the bronchoalveolar lavage fluid exosomal shuttle RNA population after lung transplantation and evaluate for differential expression between acute AR and quiescence.
Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA extraction, on which RNA-Seq was performed.
AR demonstrates an intense inflammatory environment, skewed toward both innate and adaptive immune responses. Novel, potential upstream regulators identified offer potential therapeutic targets.
Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a source for understanding the pathophysiology of AR and for biomarker discovery in lung transplantation. |
doi_str_mv | 10.1164/rccm.201503-0558OC |
format | Article |
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To provide an in-depth analysis of the bronchoalveolar lavage fluid exosomal shuttle RNA population after lung transplantation and evaluate for differential expression between acute AR and quiescence.
Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA extraction, on which RNA-Seq was performed.
AR demonstrates an intense inflammatory environment, skewed toward both innate and adaptive immune responses. Novel, potential upstream regulators identified offer potential therapeutic targets.
Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a source for understanding the pathophysiology of AR and for biomarker discovery in lung transplantation.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.201503-0558OC</identifier><identifier>PMID: 26308930</identifier><language>eng</language><publisher>United States: American Thoracic Society</publisher><subject>Acute Disease ; Adult ; Aged ; Bronchoalveolar Lavage Fluid - immunology ; Cohort Studies ; Enzyme-Linked Immunosorbent Assay ; Exosomes - immunology ; Female ; Flow Cytometry ; Graft Rejection - immunology ; Humans ; Lung - immunology ; Lung - surgery ; Lung Transplantation ; Male ; Middle Aged ; Original ; Postoperative Complications - immunology ; Reproducibility of Results ; RNA - immunology</subject><ispartof>American journal of respiratory and critical care medicine, 2015-12, Vol.192 (12), p.1490-1503</ispartof><rights>Copyright American Thoracic Society Dec 15, 2015</rights><rights>Copyright © 2015 by the American Thoracic Society 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-9336856dedd65beeab69793a79812005fe9228ad9835b3517a55e85ea25a88eb3</citedby><cites>FETCH-LOGICAL-c430t-9336856dedd65beeab69793a79812005fe9228ad9835b3517a55e85ea25a88eb3</cites><orcidid>0000-0001-6806-0868 ; 0000-0001-7021-8273</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,4011,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26308930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gregson, Aric L</creatorcontrib><creatorcontrib>Hoji, Aki</creatorcontrib><creatorcontrib>Injean, Patil</creatorcontrib><creatorcontrib>Poynter, Steven T</creatorcontrib><creatorcontrib>Briones, Claudia</creatorcontrib><creatorcontrib>Palchevskiy, Vyacheslav</creatorcontrib><creatorcontrib>Weigt, S Sam</creatorcontrib><creatorcontrib>Shino, Michael Y</creatorcontrib><creatorcontrib>Derhovanessian, Ariss</creatorcontrib><creatorcontrib>Sayah, David</creatorcontrib><creatorcontrib>Saggar, Rajan</creatorcontrib><creatorcontrib>Ross, David</creatorcontrib><creatorcontrib>Ardehali, Abbas</creatorcontrib><creatorcontrib>Lynch, 3rd, Joseph P</creatorcontrib><creatorcontrib>Belperio, John A</creatorcontrib><title>Altered Exosomal RNA Profiles in Bronchoalveolar Lavage from Lung Transplants with Acute Rejection</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>The mechanism by which acute allograft rejection leads to chronic rejection remains poorly understood despite its common occurrence. Exosomes, membrane vesicles released from cells within the lung allograft, contain a diverse array of biomolecules that closely reflect the biologic state of the cell and tissue from which they are released. Exosome transcriptomes may provide a better understanding of the rejection process. Furthermore, biomarkers originating from this transcriptome could provide timely and sensitive detection of acute cellular rejection (AR), reducing the incidence of severe AR and chronic lung allograft dysfunction and improving outcomes.
To provide an in-depth analysis of the bronchoalveolar lavage fluid exosomal shuttle RNA population after lung transplantation and evaluate for differential expression between acute AR and quiescence.
Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA extraction, on which RNA-Seq was performed.
AR demonstrates an intense inflammatory environment, skewed toward both innate and adaptive immune responses. Novel, potential upstream regulators identified offer potential therapeutic targets.
Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a source for understanding the pathophysiology of AR and for biomarker discovery in lung transplantation.</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Aged</subject><subject>Bronchoalveolar Lavage Fluid - immunology</subject><subject>Cohort Studies</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Exosomes - immunology</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Graft Rejection - immunology</subject><subject>Humans</subject><subject>Lung - immunology</subject><subject>Lung - surgery</subject><subject>Lung Transplantation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Postoperative Complications - immunology</subject><subject>Reproducibility of Results</subject><subject>RNA - immunology</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkU9v1DAQxSNERUvhC3BAlrhwSRnbcWxfkJZV-SOt2qoqEjfLcSa7WTn2YicLfHuybKmgpxlp3nuap19RvKJwQWldvUvODRcMqABeghDqevmkOKOCi7LSEp7OO0heVpX-dlo8z3kLQJmi8Kw4ZTUHpTmcFc3Cj5iwJZc_Y46D9eT2akFuUux6j5n0gXxIMbhNtH6P0dtEVnZv10i6FAeymsKa3CUb8s7bMGbyox83ZOGmEcktbtGNfQwvipPO-owv7-d58fXj5d3yc7m6_vRluViVruIwlprzWom6xbatRYNom1pLza3UijIA0aFmTNlWKy4aLqi0QqASaJmwSmHDz4v3x9zd1AzYOgxjst7sUj_Y9MtE25v_L6HfmHXcm0pyKqmeA97eB6T4fcI8mqHPDv1cDeOUDZUCAJhm1Sx980i6jVMKc70_Ki5nKIdAdlS5FHNO2D08Q8EcEJoDQnNEaI4IZ9Prf2s8WP4y478BwseZCA</recordid><startdate>20151215</startdate><enddate>20151215</enddate><creator>Gregson, Aric L</creator><creator>Hoji, Aki</creator><creator>Injean, Patil</creator><creator>Poynter, Steven T</creator><creator>Briones, Claudia</creator><creator>Palchevskiy, Vyacheslav</creator><creator>Weigt, S Sam</creator><creator>Shino, Michael Y</creator><creator>Derhovanessian, Ariss</creator><creator>Sayah, David</creator><creator>Saggar, Rajan</creator><creator>Ross, David</creator><creator>Ardehali, Abbas</creator><creator>Lynch, 3rd, Joseph P</creator><creator>Belperio, John A</creator><general>American Thoracic 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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6806-0868</orcidid><orcidid>https://orcid.org/0000-0001-7021-8273</orcidid></search><sort><creationdate>20151215</creationdate><title>Altered Exosomal RNA Profiles in Bronchoalveolar Lavage from Lung Transplants with Acute Rejection</title><author>Gregson, Aric L ; 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Exosomes, membrane vesicles released from cells within the lung allograft, contain a diverse array of biomolecules that closely reflect the biologic state of the cell and tissue from which they are released. Exosome transcriptomes may provide a better understanding of the rejection process. Furthermore, biomarkers originating from this transcriptome could provide timely and sensitive detection of acute cellular rejection (AR), reducing the incidence of severe AR and chronic lung allograft dysfunction and improving outcomes.
To provide an in-depth analysis of the bronchoalveolar lavage fluid exosomal shuttle RNA population after lung transplantation and evaluate for differential expression between acute AR and quiescence.
Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA extraction, on which RNA-Seq was performed.
AR demonstrates an intense inflammatory environment, skewed toward both innate and adaptive immune responses. Novel, potential upstream regulators identified offer potential therapeutic targets.
Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a source for understanding the pathophysiology of AR and for biomarker discovery in lung transplantation.</abstract><cop>United States</cop><pub>American Thoracic Society</pub><pmid>26308930</pmid><doi>10.1164/rccm.201503-0558OC</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-6806-0868</orcidid><orcidid>https://orcid.org/0000-0001-7021-8273</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Adult Aged Bronchoalveolar Lavage Fluid - immunology Cohort Studies Enzyme-Linked Immunosorbent Assay Exosomes - immunology Female Flow Cytometry Graft Rejection - immunology Humans Lung - immunology Lung - surgery Lung Transplantation Male Middle Aged Original Postoperative Complications - immunology Reproducibility of Results RNA - immunology |
title | Altered Exosomal RNA Profiles in Bronchoalveolar Lavage from Lung Transplants with Acute Rejection |
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