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dc.creatorAksoy, Mark O.
dc.creatorKim, Victor
dc.creatorCornwell, William D.
dc.creatorRogers, Thomas J.
dc.creatorKosmider, Beata
dc.creatorBahmed, Karim
dc.creatorBarrero, Carlos
dc.creatorMerali, Salim
dc.creatorShetty, Neena
dc.creatorKelsen, Steven
dc.date.accessioned2023-06-22T15:11:37Z
dc.date.available2023-06-22T15:11:37Z
dc.date.issued2017-05-02
dc.identifier.citationAksoy, M.O., Kim, V., Cornwell, W.D. et al. Secretion of the endoplasmic reticulum stress protein, GRP78, into the BALF is increased in cigarette smokers. Respir Res 18, 78 (2017). https://doi.org/10.1186/s12931-017-0561-6
dc.identifier.issn1465-993X
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/8744
dc.identifier.urihttp://hdl.handle.net/20.500.12613/8780
dc.description.abstractBackground: Identification of biomarkers of cigarette smoke –induced lung damage and early COPD is an area of intense interest. Glucose regulated protein of 78 kD (i.e., GRP78), a multi-functional protein which mediates cell responses to oxidant stress, is increased in the lungs of cigarette smokers and in the serum of subjects with COPD. We have suggested that secretion of GRP78 by lung cells may explain the increase in serum GRP78 in COPD. To assess GRP78 secretion by the lung, we assayed GRP78 in bronchoalveolar lavage fluid (BALF) in chronic smokers and non-smokers. We also directly assessed the acute effect of cigarette smoke material on GRP78 secretion in isolated human airway epithelial cells (HAEC). Methods: GRP78 was measured in BALF of smokers (S; n = 13) and non-smokers (NS; n = 11) by Western blotting. GRP78 secretion by HAEC was assessed by comparing its concentration in cell culture medium and cell lysates. Cells were treated for 24 h with either the volatile phase of cigarette smoke (cigarette smoke extract (CSE) or the particulate phase (cigarette smoke condensate (CSC)). Results: GRP78 was present in the BALF of both NS and S but levels were significantly greater in S (p = 0.04). GRP78 was secreted constitutively in HAEC. CSE 15% X 24 h increased GRP78 in cell-conditioned medium without affecting its intracellular concentration. In contrast, CSC X 24 h increased intracellular GRP78 expression but did not affect GRP78 secretion. Brefeldin A, an inhibitor of classical Golgi secretion pathways, did not inhibit GRP78 secretion indicating that non-classical pathways were involved. Conclusion: The present study indicates that GRP78 is increased in BALF in cigarette smokers; that HAEC secrete GRP78; and that GRP78 secretion by HAEC is augmented by cigarette smoke particulates. Enhanced secretion of GRP78 by lung cells makes it a potential biomarker of cigarette smoke–induced lung injury.
dc.format.extent8 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofFaculty/ Researcher Works
dc.relation.haspartRespiratory Research, Vol. 18
dc.relation.isreferencedbyBMC
dc.rightsAttribution CC BY
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectOxidant stress
dc.subjectGRP78
dc.subjectCigarette smoke
dc.subjectCOPD
dc.subjectHistone deacetylase
dc.subjectBiomarker
dc.subjectHuman
dc.subjectLung
dc.titleSecretion of the endoplasmic reticulum stress protein, GRP78, into the BALF is increased in cigarette smokers
dc.typeText
dc.type.genreJournal article
dc.contributor.groupCenter for Inflammation, Translational and Clinical Lunch Research (Temple University)
dc.description.departmentThoracic Medicine and Surgery
dc.description.departmentPhysiology
dc.relation.doihttps://doi.org/10.1186/s12931-017-0561-6
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeLewis Katz School of Medicine
dc.description.schoolcollegeTemple University. School of Pharmacy
dc.creator.orcidKosmider|0000-0001-7421-5424
dc.creator.orcidBarrero|0000-0001-5779-6642
dc.creator.orcidMerali|0000-0002-0280-5289
dc.creator.orcidKelsen|0000-0002-5214-145X
dc.temple.creatorAksoy, Mark O.
dc.temple.creatorKim, Victor
dc.temple.creatorCornwell, William D.
dc.temple.creatorRogers, Thomas J.
dc.temple.creatorKosmider, Beata
dc.temple.creatorBahmed, Karim
dc.temple.creatorBarrero, Carlos A.
dc.temple.creatorMerali, Salim
dc.temple.creatorShetty, Neena
dc.temple.creatorKelsen, Steven G.
refterms.dateFOA2023-06-22T15:11:37Z


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