ISSN:
0021-9541
Keywords:
Life and Medical Sciences
;
Cell & Developmental Biology
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Biology
,
Medicine
Notes:
High concentrations of zinc salts (500 m̈M and greater) are known to inhibit apoptosis in a variety of systems. However, closer examination of dose effects revealed that lower concentrations of zinc (80-200 m̈M) could induce apoptosis in approximately 30-40% of mouse thymocytes following 8 h incubation. The ability of zinc to cause thymocyte apoptosis was detected flow-cytometrically by reductions in propidium iodide DNA fluorescence and forward scatter, both quantitative indicators of apoptotic death. Zinc induced both internucleosomal DNA fragmentation and morphological changes characteristic of apoptosis as determined by gel electrophoresis and electron microscopy, respectively. In addition, transcriptional and translational inhibitors prevented zinc-induced apoptosis, indicating a requirement for de novo mRNA and protein synthesis, another characteristic of apoptotic death. Fluorescent immunophenotype-specific apoptotic analysis indicated that zinc-induced apoptosis occurred primarily in the less mature CD4+CD8+αb̃TCRIoCD3εIo thymocyte subset, with lower amounts of death occurring in the other subsets. This lineage specificity was shared with glucocorticoid-induced apoptosis. Taken together, these results indicate that zinc induces true apopotitic death in mouse thymocytes and suggests a role for zinc in the regulation of apoptosis. © 1995 Wiley-Liss, Inc.
Additional Material:
8 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/jcp.1041640206
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