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Effects of chromic chloride on chick embryo fibroblast viability

The objective of this study is to evaluate the effects of chromic chloride (CrCl(3)) on chick embryo fibroblast (CEF) viability. The cells were incubated with CrCl(3) (0.02, 0.1, 0.5, 2.5, 12.5, and 62.5 μM), and the viability was determined using MTT assay, morphological detection and flow cytometr...

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Detalles Bibliográficos
Autores principales: Liu, Mingchao, Liu, Yanhan, Cheng, Ziqiang, Liu, Jianzhu, Chai, Tongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598472/
https://www.ncbi.nlm.nih.gov/pubmed/28962390
http://dx.doi.org/10.1016/j.toxrep.2015.03.007
Descripción
Sumario:The objective of this study is to evaluate the effects of chromic chloride (CrCl(3)) on chick embryo fibroblast (CEF) viability. The cells were incubated with CrCl(3) (0.02, 0.1, 0.5, 2.5, 12.5, and 62.5 μM), and the viability was determined using MTT assay, morphological detection and flow cytometry. The results show that lower concentrations of CrCl(3) (0.02, 0.1, and 0.5 μM) did not damage CEF viability. At 0.1 μM, CrCl(3) can increase CEF viability (P < 0.05). However, at higher concentrations of CrCl(3) (2.5, 12.5, and 62.5 μM), the number of apoptotic and necrotic cells (P < 0.01) and intracellular reactive oxygen species (P < 0.01) increased. In addition, decreased mitochondrial membrane potential (P < 0.01) and enhanced intracellular calcium levels (P < 0.01) were observed after the exposure. Moreover, apoptotic morphological changes induced by these processes in CEF were confirmed using Hoechst 33258 staining. Cell death induced by higher concentrations of CrCl(3) was caused by an apoptotic and a necrotic mechanism, whereas the main mechanism of oxidative stress and induced mitochondrial dysfunction was apoptotic death. The induced apoptotic death in CEF is concentration- and time-dependent.