Effects of PCB 52 and PCB 77 on cell viability, [Ca2+]i levels and membrane fluidity in mouse thymocytes
| dc.contributor.author | Yilmaz, B | |
| dc.contributor.author | Sandal, S | |
| dc.contributor.author | Chen, CH | |
| dc.contributor.author | Carpenter, DO | |
| dc.date.accessioned | 2026-08-12T17:44:27Z | |
| dc.date.issued | 2006 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | Exposure to polychlorinated biphenyls (PCBs) is known to suppress immune system function and this action is usually ascribed to dioxin-like PCBs that act via the Ah receptor. We have studied the effects of one ortho-substituted, non-dioxin-like PCB (PCB 52) and one coplanar, dioxin-like congener (PCB 77) on properties of thymocytes acutely isolated front mice, Viability of thymocytes was dose- and time-dependently reduced by PCB 52 with a threshold concentration of about 1 mu M, while there was no effect of PCB 77 on viability at concentrations less than 10 mu M. Cell death was detectible within 5 min of exposure. Both congeners caused a dose-dependent increase in [Ca2+](i), but the threshold concentration was 1 mu M for PCB 52 and 5 mu M for PCB 77, However, the cell death was not due to the elevation of [Ca2+](i), since it was not reduced by incubation in Ca-free Tyrode's Solution. PCB 52, but not PCB 77, caused an increase in membrane fluidity at a concentration of 5 mu M. These observations are consistent with previous results that suggest that ortho-substituted PCB congeners dissolve in cell membrane and cause greater disruption of function than do dioxin-like PCB congeners. (c) 2005 Elsevier Ireland Ltd. All rights reserved. | |
| dc.identifier.doi | 10.1016/j.tox.2005.09.008 | |
| dc.identifier.endpage | 193 | |
| dc.identifier.issn | 0300-483X | |
| dc.identifier.issn | 1879-3185 | |
| dc.identifier.issue | 2.Mar | |
| dc.identifier.orcid | 0000-0002-2674-6535 | |
| dc.identifier.pmid | 16233944 | |
| dc.identifier.scopus | 2-s2.0-28844441923 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 184 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tox.2005.09.008 | |
| dc.identifier.uri | https://hdl.handle.net/11508/60258 | |
| dc.identifier.volume | 217 | |
| dc.identifier.wos | WOS:000234743800011 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Ireland Ltd | |
| dc.relation.ispartof | Toxicology | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WoS_20260511 | |
| dc.subject | flow cytometry | |
| dc.subject | cell death | |
| dc.subject | immune function | |
| dc.subject | Ah receptor | |
| dc.title | Effects of PCB 52 and PCB 77 on cell viability, [Ca2+]i levels and membrane fluidity in mouse thymocytes | |
| dc.type | Article |







