2005
DOI: 10.1016/j.jconrel.2005.08.026
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Induction of apoptosis in macrophages by air oxidation of dioleoylphosphatidylglycerol

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Cited by 12 publications
(6 citation statements)
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“…DNA was isolated from hepatic tissue following the method of Kuo, Jan, Jeng and Chiu [ 39 ]. The tissue was homogenized in 1 ml lysis buffer [20 mM Tris-Cl (pH 7.5), 0.15 M NaCl, 1 mM EDTA, 1 mM EGTA, 1% Triton X-100, and 25 mM disodium pyrophosphate] at 37°C for 1 h. Then, 0.4 ml of saturated NaCl was added to each set of cell lysates and were incubated on ice for 5 min and centrifuged at 3,000 × g for 30 min.…”
Section: Methodsmentioning
confidence: 99%
“…DNA was isolated from hepatic tissue following the method of Kuo, Jan, Jeng and Chiu [ 39 ]. The tissue was homogenized in 1 ml lysis buffer [20 mM Tris-Cl (pH 7.5), 0.15 M NaCl, 1 mM EDTA, 1 mM EGTA, 1% Triton X-100, and 25 mM disodium pyrophosphate] at 37°C for 1 h. Then, 0.4 ml of saturated NaCl was added to each set of cell lysates and were incubated on ice for 5 min and centrifuged at 3,000 × g for 30 min.…”
Section: Methodsmentioning
confidence: 99%
“…A recent study has shown a cytotoxic effect leading to RAW 264.7 apoptosis for dioleoylphosphatidylglycerol (DOPG) used for drug delivery liposomes. The authors conclude, that this is mainly due to the oxidation of the unsaturated acyl chains [33]. However, for POPG this effect should not be as pronounced, because it has only one unsaturated acyl chain.…”
Section: Discussionmentioning
confidence: 93%
“…DNA isolation from hepatic tissue was carried out according to previously reported method [48]. The tissue was homogenized in 1 ml of lysis buffer [0.15 M NaCl, 20 mM Tris-Cl (pH 7.5), 1 mM EDTA, 1 mM EGTA, 1% Triton X-100 and 25 mM disodium pyrophosphate] at 37 °C for 1 h. Afterwards, 0.4 ml of saturated sodium chloride was added to cell lysates followed by incubation on ice for 5 min and centrifugation at 3000 rpm for 30 min.…”
Section: Methodsmentioning
confidence: 99%