Hyaluronan Export through Plasma Membranes Depends on Concurrent K+ Efflux by Kir Channels

被引:11
作者
Hagenfeld, Daniel [1 ,4 ]
Borkenhagen, Beatrice [1 ]
Schulz, Tobias [1 ]
Schillers, Hermann [2 ]
Schumacher, Udo [3 ]
Prehm, Peter [1 ]
机构
[1] Munster Univ Hosp, Inst Physiol Chem & Pathobiochem, Munster, Germany
[2] Muenster Univ Hosp, Inst Physiol 2, Munster, Germany
[3] Univ Klinikum Hamburg Eppendorf, Inst Anat Expt Morphol 2, Hamburg, Germany
[4] Univ Heidelberg Hosp, Clin Oral Dent & Maxillofacial Dis, Dept Conservat Dent, Sect Periodontol, Heidelberg, Germany
关键词
ION CHANNELS; POTASSIUM CHANNELS; MOLECULAR-MODEL; FIBROBLASTS; CELLS; ROPIVACAINE; MRP5; BUPIVACAINE; ASSOCIATION; VESICLES;
D O I
10.1371/journal.pone.0039096
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
Hyaluronan is synthesized within the cytoplasm and exported into the extracellular matrix through the cell membrane of fibroblasts by the MRP5 transporter. In order to meet the law of electroneutrality, a cation is required to neutralize the emerging negative hyaluronan charges. As we previously observed an inhibiting of hyaluronan export by inhibitors of K+ channels, hyaluronan export was now analysed by simultaneously measuring membrane potential in the presence of drugs. This was done by both hyaluronan import into inside-out vesicles and by inhibition with antisense siRNA. Hyaluronan export from fibroblast was particularly inhibited by glibenclamide, ropivacain and BaCl2 which all belong to ATP-sensitive inwardly-rectifying K-ir channel inhibitors. Import of hyaluronan into vesicles was activated by 150 mM KCl and this activation was abolished by ATP. siRNA for the K+ channels K(ir)3.4 and K(ir)6.2 inhibited hyaluronan export. Collectively, these results indicated that hyaluronan export depends on concurrent K+ efflux.
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页数:8
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