Nuclear factor-kappa B is activated in alveolar macrophages from patients with acute respiratory distress syndrome
OBJECTIVEThe expression of proinflammatory cytokines is rapidly increased in experimental models of the acute respiratory distress syndrome (ARDS), in patients at risk for ARDS, and in patients with established ARDS. Because multiple cytokines are present in bronchoalveolar lavage fluid, a common, p...
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Veröffentlicht in: | Critical care medicine 1996-08, Vol.24 (8), p.1285-1292 |
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description | OBJECTIVEThe expression of proinflammatory cytokines is rapidly increased in experimental models of the acute respiratory distress syndrome (ARDS), in patients at risk for ARDS, and in patients with established ARDS. Because multiple cytokines are present in bronchoalveolar lavage fluid, a common, proximal activation mechanism may operate in these settings. The proinflammatory cytokines whose expression is increased in the lungs of patients with ARDS have binding sequences in their enhancer/promoter regions for transcriptional regulatory proteins, such as nuclear factor-kappa B (NF-kappa B), nuclear factor-IL6 (NF-IL6), cyclic adenosine monophosphate responsive element binding protein, serum protein-1, and activating protein-1. To test the hypothesis that activation of one or more of these nuclear transcriptional regulatory factors might provide a common mechanism for the simultaneous expression of multiple cytokine genes in the setting of ARDS, we measured activation of these factors in alveolar macrophages from patients with ARDS and from controls.
DESIGNProspective, clinical study.
SETTINGMedical and surgical intensive care units at a university hospital and a county hospital.
PATIENTSTwelve patients, six with established ARDS and six control patients without lung injury.
INTERVENTIONSPatients with ARDS and controls underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Alveolar macrophages were isolated from lavage fluid and the nuclear proteins were extracted. Activation of transcriptional factors NF-kappa B, NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, and serum protein-1 was determined using an electrophoretic mobility shift assay, followed by densitometry of the autoradiographed gels.
MEASUREMENTS AND MAIN RESULTSThere were no significant differences in gender, age, tobacco smoking, Acute Physiology and Chronic Health Evaluation II score, quantity of lavage fluid, or number of alveolar macrophages in lavage specimens in the patient groups. Acute Lung Injury score and the PaO2/FIO2 ratio differed significantly between controls and ARDS patients0.46 +/- 0.17 vs. 2.74 +/- 0.14 (p < .0001) and 310 +/- 45 torr (41.3 +/- 6.0 kPa) vs. 150 +/- 11 torr (21.3 +/- 1.5 kPa) (p |
doi_str_mv | 10.1097/00003246-199608000-00004 |
format | Article |
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DESIGNProspective, clinical study.
SETTINGMedical and surgical intensive care units at a university hospital and a county hospital.
PATIENTSTwelve patients, six with established ARDS and six control patients without lung injury.
INTERVENTIONSPatients with ARDS and controls underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Alveolar macrophages were isolated from lavage fluid and the nuclear proteins were extracted. Activation of transcriptional factors NF-kappa B, NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, and serum protein-1 was determined using an electrophoretic mobility shift assay, followed by densitometry of the autoradiographed gels.
MEASUREMENTS AND MAIN RESULTSThere were no significant differences in gender, age, tobacco smoking, Acute Physiology and Chronic Health Evaluation II score, quantity of lavage fluid, or number of alveolar macrophages in lavage specimens in the patient groups. Acute Lung Injury score and the PaO2/FIO2 ratio differed significantly between controls and ARDS patients0.46 +/- 0.17 vs. 2.74 +/- 0.14 (p < .0001) and 310 +/- 45 torr (41.3 +/- 6.0 kPa) vs. 150 +/- 11 torr (21.3 +/- 1.5 kPa) (p <.006), respectively. The mean FIO2 of the control patients was not significantly different from the mean FIO2 of ARDS patients0.47 +/- 0.11 vs. 0.55 +/- 0.6 (p = .53). Patients with ARDS had significantly (p < .02) increased activation of NF-kappa B in alveolar macrophages compared with patients without the syndrome. There was no evidence of increased activation of the transcriptional factors activating protein-1, serum protein-1, NF-IL6, or cyclic adenosine monophosphate responsive element binding protein in alveolar macrophages from ARDS vs. control patients.
CONCLUSIONSThese experiments demonstrated increased in vivo activation of the nuclear transcriptional regulatory factor NF-kappa B (but not NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, or serum protein-1) in alveolar macrophages from patients with ARDS. Because binding sequences for NF-kappa B are present in the enhancer/promoter sequences of multiple proinflammatory cytokines, activation of NF-kappa B may contribute to the increased expression of multiple cytokines in the lung in the setting of established ARDS.(Crit Care Med 1996; 24:1285-1292)</description><identifier>ISSN: 0090-3493</identifier><identifier>EISSN: 1530-0293</identifier><identifier>DOI: 10.1097/00003246-199608000-00004</identifier><identifier>PMID: 8706481</identifier><identifier>CODEN: CCMDC7</identifier><language>eng</language><publisher>Hagerstown, MD: Williams & Wilkins</publisher><subject>Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Base Sequence ; Biological and medical sciences ; Emergency and intensive respiratory care ; Female ; Humans ; Intensive care medicine ; Macrophages, Alveolar - metabolism ; Male ; Medical sciences ; Middle Aged ; Molecular Sequence Data ; NF-kappa B - genetics ; NF-kappa B - metabolism ; Prospective Studies ; Respiratory Distress Syndrome, Adult - genetics ; Respiratory Distress Syndrome, Adult - metabolism ; Severity of Illness Index ; Transcriptional Activation</subject><ispartof>Critical care medicine, 1996-08, Vol.24 (8), p.1285-1292</ispartof><rights>Williams & Wilkins 1996. All Rights Reserved.</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3844-6dcc3b9da6b2a93e8d0394c88fef77520a0d72ef273775d521a4ca3ef02cc95a3</citedby><cites>FETCH-LOGICAL-c3844-6dcc3b9da6b2a93e8d0394c88fef77520a0d72ef273775d521a4ca3ef02cc95a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3196386$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8706481$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwartz, Michael D</creatorcontrib><creatorcontrib>Moore, Ernest E</creatorcontrib><creatorcontrib>Moore, Frederick A</creatorcontrib><creatorcontrib>Shenkar, Robert</creatorcontrib><creatorcontrib>Moine, Pierre</creatorcontrib><creatorcontrib>Haenel, James B</creatorcontrib><creatorcontrib>Abraham, Edward</creatorcontrib><title>Nuclear factor-kappa B is activated in alveolar macrophages from patients with acute respiratory distress syndrome</title><title>Critical care medicine</title><addtitle>Crit Care Med</addtitle><description>OBJECTIVEThe expression of proinflammatory cytokines is rapidly increased in experimental models of the acute respiratory distress syndrome (ARDS), in patients at risk for ARDS, and in patients with established ARDS. Because multiple cytokines are present in bronchoalveolar lavage fluid, a common, proximal activation mechanism may operate in these settings. The proinflammatory cytokines whose expression is increased in the lungs of patients with ARDS have binding sequences in their enhancer/promoter regions for transcriptional regulatory proteins, such as nuclear factor-kappa B (NF-kappa B), nuclear factor-IL6 (NF-IL6), cyclic adenosine monophosphate responsive element binding protein, serum protein-1, and activating protein-1. To test the hypothesis that activation of one or more of these nuclear transcriptional regulatory factors might provide a common mechanism for the simultaneous expression of multiple cytokine genes in the setting of ARDS, we measured activation of these factors in alveolar macrophages from patients with ARDS and from controls.
DESIGNProspective, clinical study.
SETTINGMedical and surgical intensive care units at a university hospital and a county hospital.
PATIENTSTwelve patients, six with established ARDS and six control patients without lung injury.
INTERVENTIONSPatients with ARDS and controls underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Alveolar macrophages were isolated from lavage fluid and the nuclear proteins were extracted. Activation of transcriptional factors NF-kappa B, NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, and serum protein-1 was determined using an electrophoretic mobility shift assay, followed by densitometry of the autoradiographed gels.
MEASUREMENTS AND MAIN RESULTSThere were no significant differences in gender, age, tobacco smoking, Acute Physiology and Chronic Health Evaluation II score, quantity of lavage fluid, or number of alveolar macrophages in lavage specimens in the patient groups. Acute Lung Injury score and the PaO2/FIO2 ratio differed significantly between controls and ARDS patients0.46 +/- 0.17 vs. 2.74 +/- 0.14 (p < .0001) and 310 +/- 45 torr (41.3 +/- 6.0 kPa) vs. 150 +/- 11 torr (21.3 +/- 1.5 kPa) (p <.006), respectively. The mean FIO2 of the control patients was not significantly different from the mean FIO2 of ARDS patients0.47 +/- 0.11 vs. 0.55 +/- 0.6 (p = .53). Patients with ARDS had significantly (p < .02) increased activation of NF-kappa B in alveolar macrophages compared with patients without the syndrome. There was no evidence of increased activation of the transcriptional factors activating protein-1, serum protein-1, NF-IL6, or cyclic adenosine monophosphate responsive element binding protein in alveolar macrophages from ARDS vs. control patients.
CONCLUSIONSThese experiments demonstrated increased in vivo activation of the nuclear transcriptional regulatory factor NF-kappa B (but not NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, or serum protein-1) in alveolar macrophages from patients with ARDS. Because binding sequences for NF-kappa B are present in the enhancer/promoter sequences of multiple proinflammatory cytokines, activation of NF-kappa B may contribute to the increased expression of multiple cytokines in the lung in the setting of established ARDS.(Crit Care Med 1996; 24:1285-1292)</description><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Emergency and intensive respiratory care</subject><subject>Female</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Macrophages, Alveolar - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - metabolism</subject><subject>Prospective Studies</subject><subject>Respiratory Distress Syndrome, Adult - genetics</subject><subject>Respiratory Distress Syndrome, Adult - metabolism</subject><subject>Severity of Illness Index</subject><subject>Transcriptional Activation</subject><issn>0090-3493</issn><issn>1530-0293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU2PFCEQhonRrOOuP8GEg_HWCg3dwFE3fiWb3Yt77tRA4eDSHwK9k_n3ss44N7mQt-p5q8ILIZSz95wZ9YHVI1rZN9yYnumqmqeSfEY2vBNVtEY8JxvGDGuENOIleZXzL8a47JS4IBdasV5qviHpdrURIVEPtsypeYBlAfqJhkxrITxCQUfDRCE-4hwrN4JN87KDn5ipT_NIFygBp5LpPpRdNa0FacK8hAR14IG6kEvVmebD5KoBr8gLDzHj69N9Se6_fP5x_a25ufv6_frjTWOFlrLpnbViaxz02xaMQO2YMNJq7dEr1bUMmFMt-laJKl3XcpAWBHrWWms6EJfk3XHukubfK-YyjCFbjBEmnNc8KN1yqXtVQX0E68tyTuiHJYUR0mHgbHiKe_gX93CO-29JVuub0451O6I7G0_51v7bUx-yhegTTDbkMya46YXuKyaP2H6OBVN-iOse07BDiGU3_O-zxR9KvZl5</recordid><startdate>199608</startdate><enddate>199608</enddate><creator>Schwartz, Michael D</creator><creator>Moore, Ernest E</creator><creator>Moore, Frederick A</creator><creator>Shenkar, Robert</creator><creator>Moine, Pierre</creator><creator>Haenel, James B</creator><creator>Abraham, Edward</creator><general>Williams & Wilkins</general><general>Lippincott</general><scope>IQODW</scope><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></search><sort><creationdate>199608</creationdate><title>Nuclear factor-kappa B is activated in alveolar macrophages from patients with acute respiratory distress syndrome</title><author>Schwartz, Michael D ; Moore, Ernest E ; Moore, Frederick A ; Shenkar, Robert ; Moine, Pierre ; Haenel, James B ; Abraham, Edward</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3844-6dcc3b9da6b2a93e8d0394c88fef77520a0d72ef273775d521a4ca3ef02cc95a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Emergency and intensive respiratory care</topic><topic>Female</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Macrophages, Alveolar - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>NF-kappa B - genetics</topic><topic>NF-kappa B - metabolism</topic><topic>Prospective Studies</topic><topic>Respiratory Distress Syndrome, Adult - genetics</topic><topic>Respiratory Distress Syndrome, Adult - metabolism</topic><topic>Severity of Illness Index</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwartz, Michael D</creatorcontrib><creatorcontrib>Moore, Ernest E</creatorcontrib><creatorcontrib>Moore, Frederick A</creatorcontrib><creatorcontrib>Shenkar, Robert</creatorcontrib><creatorcontrib>Moine, Pierre</creatorcontrib><creatorcontrib>Haenel, James B</creatorcontrib><creatorcontrib>Abraham, Edward</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwartz, Michael D</au><au>Moore, Ernest E</au><au>Moore, Frederick A</au><au>Shenkar, Robert</au><au>Moine, Pierre</au><au>Haenel, James B</au><au>Abraham, Edward</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear factor-kappa B is activated in alveolar macrophages from patients with acute respiratory distress syndrome</atitle><jtitle>Critical care medicine</jtitle><addtitle>Crit Care Med</addtitle><date>1996-08</date><risdate>1996</risdate><volume>24</volume><issue>8</issue><spage>1285</spage><epage>1292</epage><pages>1285-1292</pages><issn>0090-3493</issn><eissn>1530-0293</eissn><coden>CCMDC7</coden><abstract>OBJECTIVEThe expression of proinflammatory cytokines is rapidly increased in experimental models of the acute respiratory distress syndrome (ARDS), in patients at risk for ARDS, and in patients with established ARDS. Because multiple cytokines are present in bronchoalveolar lavage fluid, a common, proximal activation mechanism may operate in these settings. The proinflammatory cytokines whose expression is increased in the lungs of patients with ARDS have binding sequences in their enhancer/promoter regions for transcriptional regulatory proteins, such as nuclear factor-kappa B (NF-kappa B), nuclear factor-IL6 (NF-IL6), cyclic adenosine monophosphate responsive element binding protein, serum protein-1, and activating protein-1. To test the hypothesis that activation of one or more of these nuclear transcriptional regulatory factors might provide a common mechanism for the simultaneous expression of multiple cytokine genes in the setting of ARDS, we measured activation of these factors in alveolar macrophages from patients with ARDS and from controls.
DESIGNProspective, clinical study.
SETTINGMedical and surgical intensive care units at a university hospital and a county hospital.
PATIENTSTwelve patients, six with established ARDS and six control patients without lung injury.
INTERVENTIONSPatients with ARDS and controls underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Alveolar macrophages were isolated from lavage fluid and the nuclear proteins were extracted. Activation of transcriptional factors NF-kappa B, NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, and serum protein-1 was determined using an electrophoretic mobility shift assay, followed by densitometry of the autoradiographed gels.
MEASUREMENTS AND MAIN RESULTSThere were no significant differences in gender, age, tobacco smoking, Acute Physiology and Chronic Health Evaluation II score, quantity of lavage fluid, or number of alveolar macrophages in lavage specimens in the patient groups. Acute Lung Injury score and the PaO2/FIO2 ratio differed significantly between controls and ARDS patients0.46 +/- 0.17 vs. 2.74 +/- 0.14 (p < .0001) and 310 +/- 45 torr (41.3 +/- 6.0 kPa) vs. 150 +/- 11 torr (21.3 +/- 1.5 kPa) (p <.006), respectively. The mean FIO2 of the control patients was not significantly different from the mean FIO2 of ARDS patients0.47 +/- 0.11 vs. 0.55 +/- 0.6 (p = .53). Patients with ARDS had significantly (p < .02) increased activation of NF-kappa B in alveolar macrophages compared with patients without the syndrome. There was no evidence of increased activation of the transcriptional factors activating protein-1, serum protein-1, NF-IL6, or cyclic adenosine monophosphate responsive element binding protein in alveolar macrophages from ARDS vs. control patients.
CONCLUSIONSThese experiments demonstrated increased in vivo activation of the nuclear transcriptional regulatory factor NF-kappa B (but not NF-IL6, cyclic adenosine monophosphate responsive element binding protein, activating protein-1, or serum protein-1) in alveolar macrophages from patients with ARDS. Because binding sequences for NF-kappa B are present in the enhancer/promoter sequences of multiple proinflammatory cytokines, activation of NF-kappa B may contribute to the increased expression of multiple cytokines in the lung in the setting of established ARDS.(Crit Care Med 1996; 24:1285-1292)</abstract><cop>Hagerstown, MD</cop><pub>Williams & Wilkins</pub><pmid>8706481</pmid><doi>10.1097/00003246-199608000-00004</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Base Sequence Biological and medical sciences Emergency and intensive respiratory care Female Humans Intensive care medicine Macrophages, Alveolar - metabolism Male Medical sciences Middle Aged Molecular Sequence Data NF-kappa B - genetics NF-kappa B - metabolism Prospective Studies Respiratory Distress Syndrome, Adult - genetics Respiratory Distress Syndrome, Adult - metabolism Severity of Illness Index Transcriptional Activation |
title | Nuclear factor-kappa B is activated in alveolar macrophages from patients with acute respiratory distress syndrome |
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