THE MULTIDRUG RESISTANCE (MDR1) GENE-PRODUCT FUNCTIONS AS AN ATP CHANNEL

被引:365
|
作者
ABRAHAM, EH
PRAT, AG
GERWECK, L
SENEVERATNE, T
ARCECI, RJ
KRAMER, R
GUIDOTTI, G
CANTIELLO, HF
机构
[1] HARVARD UNIV,DEPT BIOCHEM & MOLEC BIOL,CAMBRIDGE,MA 02138
[2] MASSACHUSETTS GEN HOSP,RENAL UNIT,BOSTON,MA 02129
[3] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02129
[4] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
[5] CHILDRENS HOSP MED CTR,BOSTON,MA 02115
[6] HARVARD UNIV,SCH MED,JOINT CTR RADIAT THERAPY,BOSTON,MA 02115
关键词
D O I
10.1073/pnas.90.1.312
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The multidrug resistance (mdr1) gene product, P-glycoprotein, is responsible for the ATP-dependent extrusion of a variety of compounds, including chemotherapeutic drugs, from cells. The data presented here show that cells with increased levels of the P-glycoprotein release ATP to the medium in proportion to the concentration of the protein in their plasma membrane. Furthermore, measurements of whole-cell and single-channel currents with patch-clamp electrodes indicate that the P-glycoprotein serves as an ATP-conducting channel in the plasma membrane. These findings suggest an unusual role for the P-glycoprotein.
引用
收藏
页码:312 / 316
页数:5
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