Consequences of Neurite Transection in Vitro

dc.contributor.author Cengiz, Nurettin
dc.contributor.author Ozturk, Gurkan
dc.contributor.author Erdogan, Ender
dc.contributor.author Him, Aydin
dc.contributor.author Oguz, Elif Kaval
dc.date.accessioned 2025-05-10T16:48:39Z
dc.date.available 2025-05-10T16:48:39Z
dc.date.issued 2012
dc.description Erdogan, Ender/0000-0002-6220-9243; Ozturk, Gurkan/0000-0003-0352-1947; Kaval Oguz, Elif/0000-0003-0196-2693 en_US
dc.description.abstract In order to quantify degenerative and regenerative changes and analyze the contribution of multiple factors to the outcome after neurite transection, we cultured adult mouse dorsal root ganglion neurons, and with a precise laser beam, we transected the nerve fibers they extended. Cell preparations were continuously visualized for 24 h with time-lapse microscopy. More distal cuts caused a more elongated field of degeneration, while thicker neurites degenerated faster than thinner ones. Transected neurites degenerated more if the uncut neurites of the same neuron simultaneously degenerated. If any of these uncut processes regenerated, the transected neurites underwent less degeneration. Regeneration of neurites was limited to distal cuts. Unipolar neurons had shorter regeneration than multipolar ones. Branching slowed the regenerative process, while simultaneous degeneration of uncut neurites increased it. Proximal lesions, small neuronal size, and extensive and rapid neurite degeneration were predictive of death of an injured neuron, which typically displayed necrotic rather than apoptotic form. In conclusion, this in vitro model proved useful in unmasking many new aspects and correlates of mechanically-induced neurite injury. en_US
dc.description.sponsorship Yuzuncu Yil University Directorate of Scientific Research Projects [TF073] en_US
dc.description.sponsorship This study was supported by the Yuzuncu Yil University Directorate of Scientific Research Projects (grant no. TF073). en_US
dc.identifier.doi 10.1089/neu.2009.0947
dc.identifier.issn 0897-7151
dc.identifier.scopus 2-s2.0-84867501938
dc.identifier.uri https://doi.org/10.1089/neu.2009.0947
dc.identifier.uri https://hdl.handle.net/20.500.14720/1604
dc.language.iso en en_US
dc.publisher Mary Ann Liebert inc en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Axonal Injury en_US
dc.subject Axonal Regeneration en_US
dc.subject Degeneration en_US
dc.subject Neuronal Cell Death en_US
dc.title Consequences of Neurite Transection in Vitro en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Erdogan, Ender/0000-0002-6220-9243
gdc.author.id Ozturk, Gurkan/0000-0003-0352-1947
gdc.author.id Kaval Oguz, Elif/0000-0003-0196-2693
gdc.author.scopusid 55391495500
gdc.author.scopusid 57201119283
gdc.author.scopusid 7004937377
gdc.author.scopusid 15733553800
gdc.author.scopusid 57206429841
gdc.author.wosid Cengiz, Nureddin/A-4949-2018
gdc.author.wosid Him, Aydin/B-4728-2018
gdc.author.wosid Erdogan, Ender/Abc-7081-2020
gdc.author.wosid Ozturk, Gurkan/C-7035-2018
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Ozturk, Gurkan] Istanbul Medipol Univ, Dept Physiol, Sch Med, TR-34083 Istanbul, Fatih, Turkey; [Cengiz, Nurettin; Erdogan, Ender] Yuzuncu Yil Univ, Dept Histol & Embryol, Sch Med, Van, Turkey; [Ozturk, Gurkan; Him, Aydin] Yuzuncu Yil Univ, Dept Physiol, Sch Med, Van, Turkey; [Cengiz, Nurettin] Sakarya Univ, Dept Histol & Embryol, Sch Med, Sakarya, Turkey; [Erdogan, Ender] Selcuk Univ, Dept Histol & Embryol, Sch Med, Konya, Turkey; [Him, Aydin] Ondokuz Mayis Univ, Dept Physiol, Sch Med, Samsun, Turkey; [Oguz, Elif Kaval] Yuzuncu Yil Univ, Dept Primary Educ, Fac Educ, Van, Turkey en_US
gdc.description.endpage 2474 en_US
gdc.description.issue 15 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 2465 en_US
gdc.description.volume 29 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 20121423
gdc.identifier.wos WOS:000309967300004
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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