Publication:
Neuroangiogenesis potential of mesenchymal stem cell extracellular vesicles in ischemic stroke conditions

dc.contributor.coauthorMirzaahmadi, Behnaz
dc.contributor.coauthorAhmadian, Shahin
dc.contributor.coauthorHaddadi, Parinaz
dc.contributor.coauthorNezhad-Mokhtari, Parinaz
dc.contributor.coauthorNezamdoust, Fereshteh Vaziri
dc.contributor.coauthorYalameha, Banafsheh
dc.contributor.coauthorChegeni, Sara Aghakhani
dc.contributor.coauthorRashidi, Somayyeh
dc.contributor.coauthorMousakhani, Akbar
dc.contributor.coauthorShafaei, Hajar
dc.contributor.coauthorRahbarghazi, Reza
dc.contributor.coauthorKarimipour, Mohammad
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.kuauthorFaculty Member, Sokullu, Emel
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2025-09-10T04:56:44Z
dc.date.available2025-09-09
dc.date.issued2025
dc.description.abstractIschemic stroke (IS) is a life-threatening condition in humans with high morbidity and mortality rates in developing and industrialized countries. The occlusion of blood-supporting vessels by thrombus or emboli can contribute to massive brain cell damage, neurological deficits, and long-term disability, and in more severe conditions, results in sudden death. Current therapeutic strategies, along with rehabilitation, in part, but not completely, can restore the integrity and function of the brain. These features necessitate the advent of novel therapeutic protocols for yielding better regenerative outcomes in IS patients. In past decades, the discovery of stem cells and byproducts has led to promising results in in vitro settings and pre-clinical studies. Extracellular vesicles (EVs) are nano-sized particles released from various cell types, for instance, mesenchymal stem cells (MSCs), with certain signaling biomolecules, growth factors, and cytokines involved in cell-to-cell communication. A great plethora of studies have pointed to the fact that EVs with specific cargo can distribute easily in different parts of the body, making them appropriate therapeutics under different pathological conditions. The current review articles aimed to highlight the neuroangiogenesis properties of MSC EVs in IS conditions. How and by which mechanisms MSC EVs can orchestrate the process of nervous system regeneration is at the center of debate. We think that the current article can help us better understand MSC EVs' function in the restoration of brain function under IS conditions in terms of neurogenesis and angiogenesis.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipTabriz University of Medical Sciences
dc.description.versionPublished Version
dc.description.volume23
dc.identifier.doi10.1186/s12964-025-02286-w
dc.identifier.eissn1478-811X
dc.identifier.embargoNo
dc.identifier.filenameinventorynoIR06401
dc.identifier.issue1
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-105007558119
dc.identifier.urihttps://doi.org/10.1186/s12964-025-02286-w
dc.identifier.urihttps://hdl.handle.net/20.500.14288/30191
dc.identifier.wos001503497900001
dc.keywordsIschemic stroke
dc.keywordsExtracellular vesicles
dc.keywordsNeuroangiogenesis
dc.keywordsTherapeutics
dc.keywordsBrain
dc.keywordsRegeneration
dc.language.isoeng
dc.publisherBMC
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofCell Communication and Signaling
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCell biology
dc.titleNeuroangiogenesis potential of mesenchymal stem cell extracellular vesicles in ischemic stroke conditions
dc.typeReview
dspace.entity.typePublication
relation.isOrgUnitOfPublication91bbe15d-017f-446b-b102-ce755523d939
relation.isOrgUnitOfPublication.latestForDiscovery91bbe15d-017f-446b-b102-ce755523d939
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