Evaluation of common housekeeping proteins under ischemic conditions and/or rt-PA treatment in bEnd.3 cells

UDC.coleccionInvestigación
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicas
UDC.endPage15
UDC.grupoInvEnfermidades Cerebrovasculares: Neuroloxía Clínica e Traslacional (INIBIC)
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruña
UDC.journalTitleJournal of Proteomics
UDC.startPage10
UDC.volume184
dc.contributor.authorComajoan, Pau
dc.contributor.authorGubern, Carme
dc.contributor.authorHuguet, Gemma
dc.contributor.authorSerena, Joaquín
dc.contributor.authorKádár, Elisabet
dc.contributor.authorCastellanos, María del Mar
dc.date.accessioned2026-03-24T12:27:04Z
dc.date.available2026-03-24T12:27:04Z
dc.date.issued2018-06-18
dc.description.abstract[Abstract] Thrombolysis with recombinant tissue plasminogen activator (rt-PA) is the only pharmacological approved treatment for ischemic stroke, despite its associated increasing risk of hemorrhagic transformation. Since many of rt-PA effects in blood-brain barrier (BBB) are not well characterized, the study of protein changes in BBB cells after rt-PA administration may help to understand its adverse effects. Our aim was to analyze protein levels of four commonly used housekeeping proteins: β-Actin, α-Tubulin, GAPDH and HPRT in bEnd.3 endothelial cell line subjected to oxygen and glucose deprivation (OGD) conditions and rt-PA treatment to determine their reliability as Western blot loading controls. bEnd.3 monolayers were subjected to 2.5 h of OGD and reperfusion with/without 20 μg/ml of rt-PA. At 3, 6, 24 and 72 h post-OGD, protein levels were analyzed by Western blot using Stain-Free technology. OGD significantly decreased β-Actin, α-Tubulin, GAPDH and HPRT protein levels at 3, 6, 24 and 72 h post-OGD without significant rt-PA treatment effects except for the GAPDH levels increase in control condition at 3 h post-OGD. The present study clearly demonstrated that β-Actin, α-Tubulin, GAPDH and HPRT proteins are not suitable as loading controls for Western Blot analysis in bEnd.3 cells after OGD. Significance: We reported altered levels of β-Actin, α-Tubulin, GAPDH and HPRT housekeeping proteins in bEnd.3 endothelial cell line after an ischemic insult. Therefore, we demonstrated that these proteins are not suitable as loading controls for Western Blot analysis in our experimental conditions and we recommended the use of Stain-Free gels as an alternative to traditional housekeeping proteins normalization.
dc.description.sponsorshipThis research has been supported by the Instituto de Salud Carlos III, Health Strategic Action Program (PI13/02258) and the Spanish Stroke Research Network (RD16/0019/003) (INVICTUS and INVICTUS-PLUS). We also gratefully acknowledge grant support from Universitat de Girona (MPCUdG2016/092). P. Comajoan is supported by a predoctoral fellowship from University of Girona.
dc.identifier.citationComajoan P, Gubern C, Huguet G, Serena J, Kádár E, Castellanos M. Evaluation of common housekeeping proteins under ischemic conditions and/or rt-PA treatment in bEnd.3 cells. J Proteomics. 2018 Jul 30;184:10-15.
dc.identifier.doi10.1016/J.JPROT.2018.06.011
dc.identifier.issn1876-7737
dc.identifier.urihttps://hdl.handle.net/2183/47787
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//PI13%2F02258/ES/Transformación hemorrágica en isquemia cerebral tras administración de rt-PA: Participación de biomarcadores endoteliales y endotelio-protección mediante administración de péptidos/
dc.relation.urihttps://doi.org/10.1016/J.JPROT.2018.06.011
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectBlood brain barrier
dc.subjectEndothelial cells
dc.subjectHousekeeping proteins
dc.subjectIschemic stroke
dc.subjectOGD; rt-PA
dc.titleEvaluation of common housekeeping proteins under ischemic conditions and/or rt-PA treatment in bEnd.3 cells
dc.typejournal article
dc.type.hasVersionAM
dspace.entity.typePublication
relation.isAuthorOfPublicationfea87394-0be5-482f-b650-543f2240258c
relation.isAuthorOfPublication.latestForDiscoveryfea87394-0be5-482f-b650-543f2240258c

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