Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/41743
DC FieldValueLanguage
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.grantfulltextnone-
item.fulltextSin texto completo-
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.fullNameLópez Fernández, Daniel-
crisitem.author.fullNameClavo Varas,Bernardino-
crisitem.author.fullNameFiuza Pérez,Mª Dolores-
Appears in Collections:Artículos
Show simple item record

SCOPUSTM   
Citations

12
checked on Sep 29, 2024

WEB OF SCIENCETM
Citations

9
checked on Sep 29, 2024

Page view(s)

61
checked on Jun 29, 2024

Google ScholarTM

Check

Altmetric


Share



Export metadata



Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.