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Vol. 286, Issue 1, 305-310, July 1998
Medizinische Poliklinik, Experimentelle Nephrologie,
Universität Münster, Germany
The regulation of transport of the fluorescent organic cation
4-(4-dimethylaminostyryl)-N-methylpyridinium (ASP+) by
renal proximal tubular organic cation transport was studied in IHKE-1
and LLC-PK1 cells with a recently established fluorometric technique (, ). Stimulation of
Ca++/diacylglycerol-dependent protein kinase by
1,2-dioctanoyl glycerol (DOG; 0.01-1 µmol/l, n = 7), ATP (0.1 mmol/l, n = 9), oxytocin (0.1 µmol/l, n = 6) and bradykinin (1 µmol/l,
n = 7) resulted in an increase of ASP+
accumulation in IHKE-1 cells by 35 ± 9% (DOG), 65 ± 30%
(ATP), 66 ± 14% (bradykinin) and 70 ± 20% (oxytocin) as
compared with basal conditions, whereas ASP+ accumulation
was slightly reduced in LLC-PK1 cells after stimulation with DOG (1 µmol/l,
20 ± 7%, n = 10) and
angiotensin II (0.1 nmol/l,
20 ± 5%, n = 6). ASP+ accumulation in IHKE-1 cells also was increased by
0.5 µmol/l (20 ± 8%, n = 8) and 1 µmol/l
forskolin (35 ± 13%, n = 19), and by
8-bromo-cAMP (1 µmol/l, 125 ± 25%, n = 9),
both activators of the cAMP-dependent protein kinase (PKA). Activation
of the cGMP-dependent protein kinase (PKG) by human atrial natriuretic peptide (10 nmol/l, n = 10) or 8-bromo-cGMP (0.1 mmol/l, n = 12) resulted in an increase of 35 ± 5% and 28 ± 6%, respectively. Activation of PKA and PKG had
no influence on ASP+ transport in LLC-PK1
cells. Regulation of ASP+ uptake by these two cell lines
may be caused by direct phosphorylation of the organic cation
transporters involved or by regulation of trafficking of the
transporters to the membrane. Differences in the organic cation
transporter isoforms or alternatively, in the trafficking may
contribute to the distinct regulation of ASP+ transport in
IHKE-1 and LLC-PK1 cells.
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