Journal
CELL DEATH AND DIFFERENTIATION
Volume 9, Issue 8, Pages 790-800Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.cdd.4401034
Keywords
apoptosis; acetylcholinesterase; noncholinergic
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Funding
- NCI NIH HHS [CA 76492] Funding Source: Medline
- NIAID NIH HHS [AI 43384] Funding Source: Medline
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Acetylcholinesterase (AChE) plays a key role in terminating neurotransmission at cholinergic synapses. AChE is also found in tissues devoid of cholinergic responses, indicating potential functions beyond neurotransmission. It has been suggested that AChE may participate in development, differentiation, and pathogenic processes such as Alzheimer's disease and tumorigenesis. We examined AChE expression in a number of cell lines upon induction of apoptosis by various stimuli. AChE is induced in all apoptotic cells examined as determined by cytochemical staining, immunological analysis, affinity chromatography purification, and molecular cloning. The AChE protein was found in the cytoplasm at the initiation of apoptosis and then in the nucleus or apoptotic bodies upon commitment to cell death. Sequence analysis revealed that AChE expressed in apoptotic cells is identical to the synapse type AChE. Pharmacological inhibitors of AChE prevented apoptosis. Furthermore, blocking the expression of AChE with antisense inhibited apoptosis. Therefore, our studies demonstrate that AChE is potentially a marker and a regulator of apoptosis.
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