Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/41743
Campo DC Valoridioma
dc.contributor.authorLlontop, Pedroen_US
dc.contributor.authorLopez-Fernandez, Danielen_US
dc.contributor.authorClavo, Bernardinoen_US
dc.contributor.authorAfonso Martin, Juan Luisen_US
dc.contributor.authorFiuza-Perez, Maria D.en_US
dc.contributor.authorGarcía Arranz, Marianoen_US
dc.contributor.authorCalatayud, Joaquínen_US
dc.contributor.authorMolins López-Rodó, Laureanoen_US
dc.contributor.authorAlshehri, Khaliden_US
dc.contributor.authorAyub, Adilen_US
dc.contributor.authorRaad, Wissamen_US
dc.contributor.authorBhora, Faizen_US
dc.contributor.authorSantana-Rodriguez, Norbertoen_US
dc.contributor.otherLOPEZ FERNANDEZ, DANIEL
dc.date.accessioned2018-08-03T10:39:34Z-
dc.date.available2018-08-03T10:39:34Z-
dc.date.issued2018en_US
dc.identifier.issn1081-5589en_US
dc.identifier.urihttp://hdl.handle.net/10553/41743-
dc.description.abstractIdiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with poor prognosis. Adipose-derived stem cells (ADSC) have demonstrated regenerative properties in several tissues. The hypothesis of this study was that airway transplantation of ADSC could protect against bleomycin (BLM)-induced pulmonary fibrosis (PF). Fifty-eight lungs from 29 male Sprague-Dawley rats were analyzed. Animals were randomly divided into five groups: a) control (n=3); b) sham (n=6); c) BLM (n=6); d) BLM+ADSC-2d (n=6); and e) BLM+ADSC-14d (n=8). Animals received 500 mu L saline (sham), 2.5 UI/kg BLM in 500 mu L saline (BLM), and 2x10(6)ADSC in 100 mu L saline intratracheally at 2 (BLM+ADSC-2d) and 14 days (BLM+ADSC-14d) after BLM. Animals were sacrificed at 28 days. Blinded Ashcroft score was used to determine pulmonary fibrosis extent on histology. Hsp27, Vegf, Nfk, IL-1, IL-6, Col4, and Tgf1 mRNA gene expression were determined using real-time quantitative-PCR. Ashcroft index was: control=0; sham=0.37 +/- 0.07; BLM=6.55 +/- 0.34vs sham (P=0.006). BLM vs BLM+ADSC-2d=4.63 +/- 0.38 (P=0.005) and BLM+ADSC-14d=3.77 +/- 0.46 (P=0.005). BLM vs sham significantly increased Hsp27 (P=0.018), Nfk (P=0.009), Col4 (P=0.004), Tgf1 (P=0.006) and decreased IL-1 (P=0.006). BLM+ADSC-2d vs BLM significantly decreased Hsp27 (P=0.009) and increased Vegf (P=0.006), Nfk (P=0.009). BLM+ADSC-14d vs BLM significantly decreased Hsp27 (P=0.028), IL-6 (P=0.013), Col4 (P=0.002), and increased Nfk (P=0.040) and Tgf1 (P=0.002). Airway transplantation of ADSC significantly decreased the fibrosis rate in both early and established pulmonary fibrosis, modulating the expression of Hsp27, Vegfa, Nfk, IL-6, Col4, and Tgf1. From a translational perspective, this technique could become a new adjuvant treatment for patients with IPF.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Investigative Medicineen_US
dc.sourceJournal Of Investigative Medicine[ISSN 1081-5589],v. 66 (4), p. 739-746en_US
dc.subject320508 Enfermedades pulmonaresen_US
dc.subject.otherNf-Kappa-B
dc.subject.otherTranscription Factor
dc.subject.otherGrowth-Factors
dc.subject.otherLung
dc.subject.otherModel
dc.subject.otherRat
dc.subject.otherExpression
dc.subject.otherStatement
dc.subject.otherTherapy
dc.subject.otherDisease
dc.titleAirway transplantation of adipose stem cells protects against bleomycin-induced pulmonary fibrosisen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1136/jim-2017-000494
dc.identifier.scopus85048876688
dc.identifier.isi000429735000004
dcterms.isPartOfJournal Of Investigative Medicine
dcterms.sourceJournal Of Investigative Medicine[ISSN 1081-5589],v. 66 (4), p. 739-746
dc.contributor.authorscopusid37041705700
dc.contributor.authorscopusid57211140324
dc.contributor.authorscopusid56940678900
dc.contributor.authorscopusid57190093030
dc.contributor.authorscopusid57202600785
dc.contributor.authorscopusid6507362808
dc.contributor.authorscopusid56501676000
dc.contributor.authorscopusid57202606585
dc.contributor.authorscopusid8657676900
dc.contributor.authorscopusid24390800100
dc.contributor.authorscopusid56636875400
dc.contributor.authorscopusid57190859109
dc.contributor.authorscopusid56635224400
dc.contributor.authorscopusid21833738100
dc.contributor.authorscopusid56072780900
dc.description.lastpage746-
dc.identifier.issue4-
dc.description.firstpage739-
dc.relation.volume66-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000429735000004-
dc.contributor.daisngid3257911
dc.contributor.daisngid6130827
dc.contributor.daisngid777033
dc.contributor.daisngid5321867
dc.contributor.daisngid6023199
dc.contributor.daisngid4096350
dc.contributor.daisngid34788118
dc.contributor.daisngid468673
dc.contributor.daisngid3231570
dc.contributor.daisngid4380464
dc.contributor.daisngid922353
dc.contributor.daisngid2520838
dc.contributor.daisngid479353
dc.contributor.daisngid1685892
dc.identifier.investigatorRIDD-5050-2016
dc.contributor.wosstandardWOS:Llontop, P
dc.contributor.wosstandardWOS:Lopez-Fernandez, D
dc.contributor.wosstandardWOS:Clavo, B
dc.contributor.wosstandardWOS:Martin, JLA
dc.contributor.wosstandardWOS:Fiuza-Perez, MD
dc.contributor.wosstandardWOS:Arranz, MG
dc.contributor.wosstandardWOS:Calatayud, J
dc.contributor.wosstandardWOS:Lopez-Rodo, LM
dc.contributor.wosstandardWOS:Alshehri, K
dc.contributor.wosstandardWOS:Ayub, A
dc.contributor.wosstandardWOS:Raad, W
dc.contributor.wosstandardWOS:Bhora, F
dc.contributor.wosstandardWOS:Santana-Rodriguez, N
dc.date.coverdateAbril 2018
dc.identifier.ulpgces
dc.description.sjr0,747
dc.description.jcr1,994
dc.description.sjrqQ2
dc.description.jcrqQ2
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Tecnología Médica y Audiovisual-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0003-2131-9515-
crisitem.author.orcid0000-0003-2522-1064-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameLópez Fernández, Daniel-
crisitem.author.fullNameClavo Varas,Bernardino-
crisitem.author.fullNameFiuza Pérez,Mª Dolores-
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