Human neutrophils are terminally differentiated cells that spontaneously undergo apoptosis in tissue culture. Apoptosis in these cells can be delayed by culture in the presence of granulocyte colony- stimulating factor or other inflammatory mediators. Neutrophils were found to contain an acid endonuclease that appeared to be responsible for the internucleosomal DNA cleavage that accompanies apoptosis. As measured by a plasmid nicking assay, this endonuclease had a molecular weight (M(r)) of 35,000, a pH optimum of 5.5, and a threshold for activity of pH 6.6 to 6.8. It was weakly inhibited by divalent cations (Ca2+, Mg2+, and Zn2+) and more strongly inhibited by aurintricarboxylic acid and N-bromosuccinimide. DNA from neutrophils treated with nigericin in buffers of defined pH displayed nucleosomal ladders whose prominence varied with pH in a manner that paralleled the pH dependence of the plasmid cleavage assays, consistent with internucleosomal DNA cleavage by the acid endonuclease. We have previously shown that neutrophils undergo acidification to a pH value as low as 6.0 during apoptosis; we suggest that this endonuclease may be responsible for the DNA cleavage seen in apoptotic neutrophils.
ARTICLES|
September 15, 1995
The acid deoxyribonuclease of neutrophils: a possible participant in apoptosis-associated genome destruction
RA Gottlieb,
RA Gottlieb
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA.
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HA Giesing,
HA Giesing
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA.
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RL Engler,
RL Engler
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA.
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BM Babior
BM Babior
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA.
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Blood (1995) 86 (6): 2414–2418.
Citation
RA Gottlieb, HA Giesing, RL Engler, BM Babior; The acid deoxyribonuclease of neutrophils: a possible participant in apoptosis-associated genome destruction. Blood 1995; 86 (6): 2414–2418. doi: https://doi.org/10.1182/blood.V86.6.2414.bloodjournal8662414
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