Involvement of Lipid Rafts of Rabbit Red Blood Cells in Morphological Changes Induced by Methylated β-Cyclodextrins(Biopharmacy)
スポンサーリンク
概要
- 論文の詳細を見る
Lipid rafts on cell membranes have heterogeneity such as cholesterol-rich microdomains and sphingolipids-rich microdomains. We previously reported that β-cyclodextrin (β-CyD) induced morphological changes of red blood cells (RBC) from discocyte to stomatocyte, possibly due to extraction of cholesterol from cholesterol-rich lipid rafts of RBC membranes. In this study, the effects of methyl-β-cyclodextrin (M-β-CyD) and 2,6-di-O-methyl-β-cyclodextrin (DM-β-CyD) on lipid rafts and morphological changes in rabbit RBC (RRBC) were examined, compared to those of β-CyD. In sharp contrast to β-CyD, M-β-CyD and DM-β-CyD induced morphological changes of RRBC from discocyte to echinocyte. At pre-hemolytic concentrations of β-CyDs, M-β-CyD and DM-β-CyD strongly released cholesterol from cholesterol-rich lipid rafts, compared to β-CyD. Meanwhile, the lowering effects of DM-β-CyD on fluorescent sphingomyelin analogue in sphingolipids-rich lipid rafts were more potent than those of β-CyD and M-β-CyD. The magnitude of the abilities of M-β-CyD and DM-β-CyD to extract membrane constituents was higher than that of β-CyD, consistent with that of hemolytic activity. Furthermore, DM-β-CyD and M-β-CyD, not β-CyD, lowered the amount of proteins in cholesterol-rich lipid rafts of RRBC. These results suggest that higher hemolytic activity and morphological changes from discocyte to echinocyte in RRBC induced by M-β-CyD and DM-β-CyD may be due to the extraction of both cholesterol and proteins from cholesterol-rich lipid rafts of RRBC, although DM-β-CyD may interact with sphingolipids-rich lipid rafts on RRBC membranes only slightly.
- 社団法人日本薬学会の論文
- 2009-04-01
著者
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MOTOYAMA Keiichi
Graduate School of Pharmaceutical Sciences, Kumamoto University
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TOYODOME Hiroshi
Graduate School of Pharmaceutical Sciences, Kumamoto University
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ONODERA Risako
Graduate School of Pharmaceutical Sciences, Kumamoto University
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IRIE Tetsumi
Graduate School of Pharmaceutical Sciences, Kumamoto University
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HIRAYAMA Fumitoshi
Faculty of Pharmaceutical Sciences, Sojo University
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UEKAMA Kaneto
Faculty of Pharmaceutical Sciences, Sojo University
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ARIMA Hidetoshi
Graduate School of Pharmaceutical Sciences, Kumamoto University
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有馬 英俊
熊本大学薬学部
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平山 文俊
崇城大・薬
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上釜 兼人
崇城大・薬
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上釜 兼人
熊本大・薬
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平山 文俊
熊本大学薬学部
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入江 徹美
熊本大・薬
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入江 徹美
熊本大学 薬 製剤
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上釜 兼人
熊本大学 歯
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平山 文俊
Faculty Of Pharmaceutical Sciences Sojo University
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上釜 兼人
Faculty Of Pharmaceutical Sciences Kumamoto University
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Irie T
Graduate School Of Pharmaceutical Sciences Kumamoto University
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Irie Tetsumi
Dep. Of Clinical Chemistry And Informatics Graduate School Of Pharmaceutical Sciences Kumamoto Univ.
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Onodera Risako
Graduate School Of Pharmaceutical Sciences Kumamoto University
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Irie Tetsumi
Graduate School Of Pharmaceutical Sciences Kumamoto University
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有馬 英俊
Graduate School Of Pharmaceutical Sciences Kumamoto University
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Arima Hidetoshi
School Of Pharmacy Tokyo University Of Pharmacy And Life Science
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Toyodome Hiroshi
Graduate School Of Pharmaceutical Sciences Kumamoto University
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Motoyama Keiichi
Graduate School Of Pharmaceutical Sciences Kumamoto University
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Hirayama Fumitoshi
Faculty Of Pharmaceutical Sciences Kumamoto University
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上釜 兼人
Faculty Of Pharmaceutical Sciences Sojo University
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Hirayama Fumitoshi
Faculty Of Pharmaceutical Sciences Sojo University
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Uekama Kaneto
Faculty Of Pharmaceutical Sciences Kumamoto University
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上釜 兼人
熊本大学薬学部製剤学研究室
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Hirayama F
Faculty Of Pharmaceutical Sciences Kumamoto University
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Motoyama Keiichi
Graduate School Of Pharmaceutical Sciences Kumamoto Univ.
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