Myelin Ultrastructure Terminology in Disease and Recovery Processes

dc.contributor.authorHelvacioglu, F.
dc.contributor.authorDagdeviren, A.
dc.contributor.orcIDhttps://orcid.org/0000-0002-6026-0045en_US
dc.contributor.orcIDhttps://orcid.org/0000-0001-8990-8282en_US
dc.contributor.pubmedID31821531en_US
dc.contributor.researcherIDAAH-8887-2021en_US
dc.contributor.researcherIDAES-7155-2022en_US
dc.date.accessioned2023-09-08T08:38:36Z
dc.date.available2023-09-08T08:38:36Z
dc.date.issued2019
dc.description.abstractUltrastructural evaluation of myelin coat helps to understand the possible background of pathological changes leading to deterioration or complete loss of nerve functions. A number of terms were previously introduced to describe the fine structural changes in myelin under various conditions. We believe that using a common terminology will be helpful to interpret the structure/function relationship in neurological disorders empowering the diagnosis and possible therapeutical approaches. In this paper, we present examples of ultrastructural changes in myelin during myelination, demyelination, re-myelination and dysmyelination processes and we reviewed the terminology previously used. We tried to include all studies reporting ultrastructural findings with no limitation to the experimental conditions, the species used and the disorders. The terminology used to describe the structural findings included compacted myelin, partially compacted myelin, noncompacted myelin, redundancy (hypermyelination, tomacula, myelinosome), splitting, complete circular splitting, myelin degradation, concentric lamellar bodies (myelin figures), loss of myelin lamellae, polyaxonal Schwann cells and necrotic cell debris. Ultrastructural data described in this paper aimed to provide a guide for future studies. We concluded that the evaluation of ultrastructural changes in any neurological disorder is greatly valuable for a better understanding of pathological and physiological changes occured. We also believe that supporting the ultrastructural findings with quantitative methods in the future will be of great value.en_US
dc.identifier.endpage88en_US
dc.identifier.issn0003-9829en_US
dc.identifier.issue2-3en_US
dc.identifier.scopus2-s2.0-85061846620en_US
dc.identifier.startpage77en_US
dc.identifier.urihttp://hdl.handle.net/11727/10558
dc.identifier.volume157en_US
dc.identifier.wos000528269500004en_US
dc.language.isoengen_US
dc.relation.isversionof10.12871/00039829201924en_US
dc.relation.journalARCHIVES ITALIENNES DE BIOLOGIEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSchwann cellen_US
dc.subjectMyelinationen_US
dc.subjectRe-myelinationen_US
dc.subjectDemyelinationen_US
dc.subjectDysmyelinationen_US
dc.subjectElectron microscopyen_US
dc.titleMyelin Ultrastructure Terminology in Disease and Recovery Processesen_US
dc.typeArticleen_US

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