Disintegration of lysosomes mediated by GTP γS-treated cytosol: Possible involvement of phospholipases
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概要
- 論文の詳細を見る
We showed previously that cytosol treated with guanosine 5'-O-(3-thiotriphosphate) (GTP-γS) disintegrated lysosomes in vitro in time-, temperature-, and dose-dependent manners. This also requires ATP, however, the latter can be substituted with deoxy-ATP, ADP, or ATPγS, suggesting no requirement of ATP hydrolysis. The lysis was inhibited by several chemical modifiers, including N-ethylmaleimide, 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole, and 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid, and by various phospholipase inhibitors (trifluoperazine, p-bromophenacyl bromide, nordihydroguaiaretic acid, W-7, primaquine, compound 48/80, neomycin, and gentamicin), but not by ONO-RS-082, an inhibitor of phospholipase A2. The reaction was also inhibited by phospholipids (phosphatidylinositol, phosphatidylserine, phosphatidic acid, and phosphatidylcholine) and diacylglycerol. Among the phospholipase A2 hydrolysis products of phospholipids, unsaturated fatty acids (oleate, linoleate, and arachidonate) and lysophospholipid (lysophosphatidylcholine) by themselves broke lysosomes down directly, whereas saturated fatty acids (palmitate and stearate) had little effect. We found that GTPγS-stimulated cytosolic phospholipase A2 activity was highly sensitive to ONO-RS-082. These results suggest the participation of phospholipase(s), though not cytosolic phospholipase A2, in the GTPγS-dependent lysis of lysosomes.
- 日本生化学会 = Japanese Biochemical Societyの論文
- 1998-04-01
著者
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Arai K
Jichi Medical School Tochigi
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Arai Kunizo
Faculty Of Pharmaceutical Sciences Kanazawa University
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Sai Yoshimichi
Faculty Of Pharmaceutical Sciences Kanazawa University
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Matsuda Tomoko
Faculty Of Pharmaceutical Sciences Kanazawa University
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Matsuda T
Nagoya Univ. Nagoya
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OHKUMA Shoji
Faculty of Pharmaceutical Sciences, Kanazawa University
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Ohkuma S
Kanazawa Univ. Ishikawa Jpn
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Ohkuma S.
Faculty of Pharmaceutical Sciences, Kanazawa University
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