Intranasal Administration of Undifferentiated Oligodendrocyte Lineage Cells as a Potential Approach to Deliver Oligodendrocyte Precursor Cells into Brain
Oligodendrocyte precursor cell (OPC) migration is a mechanism involved in remyelination; these cells migrate from niches in the adult CNS. However, age and disease reduce the pool of OPCs; as a result, the remyelination capacity of the CNS decreases over time. Several experimental studies have intro...
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Veröffentlicht in: | International journal of molecular sciences 2021-10, Vol.22 (19), p.10738 |
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creator | Gómez-Pinedo, Ulises Matías-Guiu, Jordi A. Benito-Martín, María Soledad Moreno-Jiménez, Lidia Sanclemente-Alamán, Inmaculada Selma-Calvo, Belen Pérez-Suarez, Sara Sancho-Bielsa, Francisco Canales-Aguirre, Alejandro Mateos-Díaz, Juan Carlos Hernández-Sapiéns, Mercedes A. Reza-Zaldívar, Edwin E. Ojeda-Hernández, Doddy Denise Vidorreta-Ballesteros, Lucía Montero-Escribano, Paloma Matías-Guiu, Jorge |
description | Oligodendrocyte precursor cell (OPC) migration is a mechanism involved in remyelination; these cells migrate from niches in the adult CNS. However, age and disease reduce the pool of OPCs; as a result, the remyelination capacity of the CNS decreases over time. Several experimental studies have introduced OPCs to the brain via direct injection or intrathecal administration. In this study, we used the nose-to brain pathway to deliver oligodendrocyte lineage cells (human oligodendroglioma (HOG) cells), which behave similarly to OPCs in vitro. To this end, we administered GFP-labelled HOG cells intranasally to experimental animals, which were subsequently euthanised at 30 or 60 days. Our results show that the intranasal route is a viable route to the CNS and that HOG cells administered intranasally migrate preferentially to niches of OPCs (clusters created during embryonic development and adult life). Our study provides evidence, albeit limited, that HOG cells either form clusters or adhere to clusters of OPCs in the brains of experimental animals. |
doi_str_mv | 10.3390/ijms221910738 |
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However, age and disease reduce the pool of OPCs; as a result, the remyelination capacity of the CNS decreases over time. Several experimental studies have introduced OPCs to the brain via direct injection or intrathecal administration. In this study, we used the nose-to brain pathway to deliver oligodendrocyte lineage cells (human oligodendroglioma (HOG) cells), which behave similarly to OPCs in vitro. To this end, we administered GFP-labelled HOG cells intranasally to experimental animals, which were subsequently euthanised at 30 or 60 days. Our results show that the intranasal route is a viable route to the CNS and that HOG cells administered intranasally migrate preferentially to niches of OPCs (clusters created during embryonic development and adult life). Our study provides evidence, albeit limited, that HOG cells either form clusters or adhere to clusters of OPCs in the brains of experimental animals.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms221910738</identifier><identifier>PMID: 34639079</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Animals ; Blood-brain barrier ; Brain cancer ; Embryogenesis ; Glial stem cells ; Intranasal administration ; Multiple sclerosis ; Myelination ; Oligodendroglioma ; Physiology ; Precursors ; Stroke ; Transplants & implants</subject><ispartof>International journal of molecular sciences, 2021-10, Vol.22 (19), p.10738</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. 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source | MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Animals Blood-brain barrier Brain cancer Embryogenesis Glial stem cells Intranasal administration Multiple sclerosis Myelination Oligodendroglioma Physiology Precursors Stroke Transplants & implants |
title | Intranasal Administration of Undifferentiated Oligodendrocyte Lineage Cells as a Potential Approach to Deliver Oligodendrocyte Precursor Cells into Brain |
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