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dc.contributor.authorKaplan, S.
dc.contributor.authorGeuna, S.
dc.contributor.authorRonchi, G.
dc.contributor.authorUlkay, M. B.
dc.contributor.authorvon Bartheld, C. S.
dc.date.accessioned2020-06-21T14:52:33Z
dc.date.available2020-06-21T14:52:33Z
dc.date.issued2010
dc.identifier.issn0165-0270
dc.identifier.issn1872-678X
dc.identifier.urihttps://doi.org/10.1016/j.jneumeth.2010.01.001
dc.identifier.urihttps://hdl.handle.net/20.500.12712/18014
dc.descriptionRonchi, Giulia/0000-0002-4795-7024; ulkay, muzaffer basak/0000-0002-0928-0462; Kaplan, Suleyman/0000-0003-1477-5002; Geuna, Stefano/0000-0002-6962-831Xen_US
dc.descriptionWOS: 000275769900014en_US
dc.descriptionPubMed: 20064555en_US
dc.description.abstractSeveral sources of variability can affect stereological estimates. Here we measured the impact of potential sources of variability on numerical stereological estimates of myelinated axons in the adult rat sciatic nerve. Besides biological variation, parameters tested included two variations of stereological methods (unbiased counting frame versus 2D-disector), two sampling schemes (few large versus frequent small sampling boxes), and workstations with varying degrees of sophistication. All estimates were validated against exhaustive counts of the same nerve cross sections to obtain calibrated true numbers of myelinated axons (gold standard). In addition, we quantified errors in particle identification by comparing light microscopic and electron microscopic images of selected consecutive sections. Biological variation was 15.6%. There was no significant difference between the two stereological approaches or workstations used, but sampling schemes with few large samples yielded larger differences (20.7 +/- 3.7% SEM) of estimates from true values, while frequent small samples showed significantly smaller differences (12.7 +/- 1.9% SEM). Particle identification was accurate in 94% of cases (range: 89-98%). The most common identification error was due to profiles of Schwann cell nuclei mimicking profiles of small myelinated nerve fibers. We recommend sampling frequent small rather than few large areas, and conclude that workstations with basic stereological equipment are sufficient to obtain accurate estimates. Electron microscopic verification showed that particle misidentification had a surprisingly variable and large impact of up to 11%, corresponding to 2/3 of the biological variation (15.6%). Thus, errors in particle identification require further attention, and we provide a simple nerve fiber recognition test to assist investigators with self-testing and training. (C) 2010 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipRegione Piemonte (Bando Ricerca Sanitaria Finalizzata)Regione Piemonte; NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [EY12841]; National Council for Research Resources [P20 RR15581]en_US
dc.description.sponsorshipThis work was supported by grants from the Regione Piemonte (Bando Ricerca Sanitaria Finalizzata), and by NIH grant EY12841, and grant P20 RR15581 (Center of Biomedical Research Excellence) from the National Council for Research Resources.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.relation.isversionof10.1016/j.jneumeth.2010.01.001en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectStereologyen_US
dc.subjectQuantificationen_US
dc.subjectBiasen_US
dc.subjectCalibrationen_US
dc.subjectMyelinated axonen_US
dc.subjectPeripheral nerveen_US
dc.subjectSamplingen_US
dc.subjectVariabilityen_US
dc.titleCalibration of the stereological estimation of the number of myelinated axons in the rat sciatic nerve: A multicenter studyen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume187en_US
dc.identifier.issue1en_US
dc.identifier.startpage90en_US
dc.identifier.endpage99en_US
dc.relation.journalJournal of Neuroscience Methodsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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