Abstract:
:Regulation of capacitative Ca(2+) entry was studied in two different multidrug resistance (MDR) protein (MRP1) overexpressing cell lines, HT29(col) and GLC4/ADR. MRP1 overexpression was accompanied by a decreased response to thapsigargin. Moreover, inhibition of capacitative Ca(2+) entry by D, L-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) was abolished in MRP1 overexpressing cells. Both PDMP and the MRP1 inhibitor MK571 greatly reduced InsP(3)-mediated (45)Ca(2+) release from intracellular stores in HT29 cells. Again, these effects were virtually abolished in HT29(col) cells. Our results point to a modulatory role of MRP1 on intracellular calcium concentration ([Ca(2+)](i)) homeostasis which may contribute to the MDR phenotype.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Filipeanu CM,Nelemans A,Veldman RJ,de Zeeuw D,Kok JWdoi
10.1016/s0014-5793(00)01585-4keywords:
subject
Has Abstractpub_date
2000-05-26 00:00:00pages
107-10issue
1eissn
0014-5793issn
1873-3468pii
S0014-5793(00)01585-4journal_volume
474pub_type
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