Publication:
IGF-1, Inflammation and Retinal Degeneration: A Close Network.

dc.contributor.authorArroba, Ana I
dc.contributor.authorCampos-Caro, Antonio
dc.contributor.authorAguilar-Diosdado, Manuel
dc.contributor.authorValverde, Angela M
dc.contributor.funderEuropean Union
dc.contributor.funderSpanish Ministry of Economy and Competitiveness
dc.contributor.funderMINECO/FEDER
dc.contributor.funderSpanish ISCIII (CIBERdem)
dc.date.accessioned2023-01-25T10:20:59Z
dc.date.available2023-01-25T10:20:59Z
dc.date.issued2018-06-14
dc.description.abstractRetinal degenerative diseases are a group of heterogeneous diseases that include age-related macular degeneration (AMD), retinitis pigmentosa (RP), and diabetic retinopathy (DR). The progressive degeneration of the retinal neurons results in a severe deterioration of the visual function. Neuroinflammation is an early hallmark of many neurodegenerative disorders of the retina including AMD, RP and DR. Microglial cells, key components of the retinal immune defense system, are activated in retinal degenerative diseases. In the microglia the interplay between the proinflammatory/classically activated or antiinflammatory/alternatively activated phenotypes is a complex dynamic process that occurs during the course of disease due to the different environmental signals related to pathophysiological conditions. In this regard, an adequate transition from the proinflammatory to the anti-inflammatory response is necessary to counteract retinal neurodegeneration and its subsequent damage that leads to the loss of visual function. Insulin like-growth factor-1 (IGF-1) has been considered as a pleiotropic factor in the retina under health or disease conditions and several effects of IGF-1 in retinal immune modulation have been described. In this review, we provide recent insights of inflammation as a common feature of retinal diseases (AMD, RP and RD) highlighting the role of microglia, exosomes and IGF-1 in this process.
dc.description.sponsorshipn. The work of AIA and ÁMV has been funded by grants from European Union (project H2020-MSCA-ITN TREATMENT Grant Agreement number: 721236 and project EUROCONDOR FP7 Grant Agreement number 278040), grant from the Spanish Ministry of Economy and Competitiveness: SAF2015-65267-R (MINECO/FEDER) and grants from the Spanish ISCIII (CIBERdem) and INFLAMES (ISCIII PIE14/00045, co-funded by ERDF, Investing in your future).
dc.description.versionSi
dc.identifier.citationArroba AI, Campos-Caro A, Aguilar-Diosdado M, Valverde ÁM. IGF-1, Inflammation and Retinal Degeneration: A Close Network. Front Aging Neurosci. 2018 Jul 5;10:203
dc.identifier.doi10.3389/fnagi.2018.00203
dc.identifier.issn1663-4365
dc.identifier.pmcPMC6041402
dc.identifier.pmid30026694
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041402/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fnagi.2018.00203/pdf
dc.identifier.urihttp://hdl.handle.net/10668/12729
dc.journal.titleFrontiers in aging neuroscience
dc.journal.titleabbreviationFront Aging Neurosci
dc.language.isoen
dc.organizationHospital Universitario Puerta del Mar
dc.organizationInstituto de Investigación e Innovación en Ciencias Biomédicas
dc.page.number12
dc.publisherFrontiers Research Foundation
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.relation.projectIDH2020-MSCA-ITN
dc.relation.projectIDSAF2015-65267-R
dc.relation.projectIDPIE14/00045
dc.relation.publisherversionhttps://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2018.00203/full
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectIGF-1
dc.subjectInflammation
dc.subjectMicroglia and exosomes
dc.subjectNeurodegeneration
dc.subjectRetina
dc.titleIGF-1, Inflammation and Retinal Degeneration: A Close Network.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number10
dspace.entity.typePublication

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