Abstract
We have recently reported that acetylcholinesterase expression was induced during apoptosis in various cell types. In the current study we provide evidence to suggest that the induction of acetylcholinesterase expression during apoptosis is regulated by the mobilization of intracellular Ca2+. During apoptosis, treatment of HeLa and MDA-MB-435s cells with the calcium ionophore A23187 resulted in a significant increase in acetylcholinesterase mRNA and protein levels. Chelation of intracellular Ca2+ by BAPTA-AM (1,2-bis-(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid-acetoxymethyl ester), an intracellular Ca2+ chelator, inhibited acetylcholinesterase expression. A23187 also enhanced the stability of acetylcholinesterase mRNA and increased the activity of acetylcholinesterase promoter, effects that were blocked by BAPTA-AM. Perturbations of cellular Ca2+ homeostasis by thapsigargin resulted in the increase of acetylcholinesterase expression as well as acetylcholinesterase promoter activity during thapsigargin induced apoptosis in HeLa and MDA-MB-435s cells, effects that were also inhibited by BAPTA-AM. We further demonstrated that the transactivation of the human acetylcholinesterase promoter by A23187 and thapsigargin was partially mediated by a CCAAT motif within the -1270 to -1248 fragment of the human acetylcholinesterase promoter. This motif was able to bind to CCAAT binding factor (CBF/NF-Y). These results strongly suggest that cytosolic Ca2+ plays a key role in acetylcholinesterase regulation during apoptosis induced by A23187 and thapsigargin.
Original language | English (US) |
---|---|
Pages (from-to) | 93-108 |
Number of pages | 16 |
Journal | International Journal of Biochemistry and Cell Biology |
Volume | 39 |
Issue number | 1 |
DOIs | |
State | Published - 2007 |
Keywords
- Acetylcholinesterase
- Apoptosis
- Ca
- Transcriptional activity
- mRNA stability
ASJC Scopus subject areas
- Biochemistry
- Cell Biology