-
1
-
-
0002955624
-
-
F. M Ashcroft and S. J. H Ashcroft, Eds. IRL Press, Oxford
-
F M. Ashcroft and S. J. H. Ashcroft, in Insulin: Molecular Biology to Pathology, F. M Ashcroft and S. J. H Ashcroft, Eds. (IRL Press, Oxford, 1992), pp 97-150.
-
(1992)
Insulin: Molecular Biology to Pathology
, pp. 97-150
-
-
Ashcroft, F.M.1
Ashcroft, S.J.H.2
-
2
-
-
0024285901
-
-
W Kramer, R. Oekonomopulos, J. Punter, H.-D. Summ, FEBS Lett. 229, 355 (1988). L. Aguilar-Bryan, D. A Nelson, Q. A. Vu, M B. Humphrey, A E Boyd, J Biol. Chem. 265, 8214 (1990); H. Bernardi et at., Proc Natl. Acad Sci U S A. 90, 1340 (1993).
-
(1988)
FEBS Lett.
, vol.229
, pp. 355
-
-
Kramer, W.1
Oekonomopulos, R.2
Punter, J.3
Summ, H.-D.4
-
3
-
-
0025343838
-
-
W Kramer, R. Oekonomopulos, J. Punter, H.-D. Summ, FEBS Lett. 229, 355 (1988). L. Aguilar-Bryan, D. A Nelson, Q. A. Vu, M B. Humphrey, A E Boyd, J Biol. Chem. 265, 8214 (1990); H. Bernardi et at., Proc Natl. Acad Sci U S A. 90, 1340 (1993).
-
(1990)
J Biol. Chem.
, vol.265
, pp. 8214
-
-
Aguilar-Bryan, L.1
Nelson, D.A.2
Vu, Q.A.3
Humphrey, M.B.4
Boyd, A.E.5
-
4
-
-
0027411218
-
-
W Kramer, R. Oekonomopulos, J. Punter, H.-D. Summ, FEBS Lett. 229, 355 (1988). L. Aguilar-Bryan, D. A Nelson, Q. A. Vu, M B. Humphrey, A E Boyd, J Biol. Chem. 265, 8214 (1990); H. Bernardi et at., Proc Natl. Acad Sci U S A. 90, 1340 (1993).
-
(1993)
Proc Natl. Acad Sci U S A
, vol.90
, pp. 1340
-
-
Bernardi, H.1
-
5
-
-
0029024314
-
-
L Aguilar-Bryan et al., Science 268, 423 (1995), N Inagaki et al., ibid 270, 1166 (1995).
-
(1995)
Science
, vol.268
, pp. 423
-
-
Aguilar-Bryan, L.1
-
6
-
-
0028972501
-
-
L Aguilar-Bryan et al., Science 268, 423 (1995), N Inagaki et al., ibid 270, 1166 (1995).
-
(1995)
Science
, vol.270
, pp. 1166
-
-
Inagaki, N.1
-
7
-
-
0028821526
-
-
S. E Ozanne, P. C. Guest, J C. Hutton, C N Hales, Diabetologia 38, 277 (1995); J. L. Carpentier, F Sawano, M. Ravazzola, W. J. Malaisse, ibid. 29, 259 (1986).
-
(1995)
Diabetologia
, vol.38
, pp. 277
-
-
Ozanne, S.E.1
Guest, P.C.2
Hutton, J.C.3
Hales, C.N.4
-
8
-
-
0022560496
-
-
S. E Ozanne, P. C. Guest, J C. Hutton, C N Hales, Diabetologia 38, 277 (1995); J. L. Carpentier, F Sawano, M. Ravazzola, W. J. Malaisse, ibid. 29, 259 (1986).
-
(1986)
Diabetologia
, vol.29
, pp. 259
-
-
Carpentier, J.L.1
Sawano, F.2
Ravazzola, M.3
Malaisse, W.J.4
-
9
-
-
0022629034
-
-
2, and 5 mM Hepes (pH 7.35 with CsOH). Electrical contact was established by insertion of the pore-forming antibiotic amphotericin B [J. Rae et al., J. Neurosci Methods 37, 15 (1991)] (final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
(1986)
Nature
, vol.319
, pp. 150
-
-
Lindau, M.1
Fernandez, J.M.2
-
10
-
-
0023795593
-
-
2, and 5 mM Hepes (pH 7.35 with CsOH). Electrical contact was established by insertion of the pore-forming antibiotic amphotericin B [J. Rae et al., J. Neurosci Methods 37, 15 (1991)] (final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
(1988)
J Gen. Physiol
, vol.92
, pp. 145
-
-
Horn, R.1
Marty, A.2
-
11
-
-
0013657423
-
-
2, and 5 mM Hepes (pH 7.35 with CsOH). Electrical contact was established by insertion of the pore-forming antibiotic amphotericin B [J. Rae et al., J. Neurosci Methods 37, 15 (1991)] (final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
(1982)
Proc Natl. Acad. Sci. U.S.A.
, vol.79
, pp. 6712
-
-
Neherand, E.1
Marty, A.2
-
12
-
-
0023905082
-
-
2, and 5 mM Hepes (pH 7.35 with CsOH)
-
2, and 5 mM Hepes (pH 7.35 with CsOH). Electrical contact was established by insertion of the pore-forming antibiotic amphotericin B [J. Rae et al., J. Neurosci Methods 37, 15 (1991)] (final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
(1988)
Biophys. J
, vol.53
, pp. 885
-
-
Joshi, C.1
Fernandez, J.2
-
13
-
-
0025775356
-
-
(final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
2, and 5 mM Hepes (pH 7.35 with CsOH). Electrical contact was established by insertion of the pore-forming antibiotic amphotericin B [J. Rae et al., J. Neurosci Methods 37, 15 (1991)] (final concentration, 0 24 mg/ml) to the pipette solution. All electrophysiological experiments were done at 32° to 34°C. Data are presented as mean values ± SEM of the stated number of experiments, and statistical evidence was evaluated with the Student's t test for paired data with each cell serving as its own control
-
(1991)
J. Neurosci Methods
, vol.37
, pp. 15
-
-
Rae, J.1
-
14
-
-
0027937697
-
-
2+ abolishes depolarization-evoked capacitance changes
-
2+ abolishes depolarization-evoked capacitance changes [C. Ammalä et al , J Physiol (London) 474, 665 (1993)] and (ii) lowering the temperature from +34°C to room temperature suppresses exocytosis (and capacitance increases) while not much affecting the properties of the voltage-gated currents (E Renström, L Eliasson, P Rorsman. in preparation).
-
(1994)
Neuron
, vol.13
, pp. 1119
-
-
Horrigan, F.T.1
Bookman, R.J.2
-
15
-
-
0027937697
-
-
and (ii) lowering the temperature from +34°C to room temperature suppresses exocytosis (and capacitance increases) while not much affecting the properties of the voltage-gated currents
-
2+ abolishes depolarization-evoked capacitance changes [C. Ammalä et al , J Physiol (London) 474, 665 (1993)] and (ii) lowering the temperature from +34°C to room temperature suppresses exocytosis (and capacitance increases) while not much affecting the properties of the voltage-gated currents (E Renström, L Eliasson, P Rorsman. in preparation).
-
(1993)
J Physiol (London)
, vol.474
, pp. 665
-
-
Ammalä, C.1
-
16
-
-
0027937697
-
-
in preparation
-
2+ abolishes depolarization-evoked capacitance changes [C. Ammalä et al , J Physiol (London) 474, 665 (1993)] and (ii) lowering the temperature from +34°C to room temperature suppresses exocytosis (and capacitance increases) while not much affecting the properties of the voltage-gated currents (E Renström, L Eliasson, P Rorsman. in preparation).
-
-
-
Renström, E.1
Eliasson, L.2
Rorsman, P.3
-
18
-
-
13344257118
-
-
note
-
+ alone) Experiments were performed at 37°C Values are means ± SEM of nine experiments carried out on three preparations of islets.
-
-
-
-
19
-
-
0025942516
-
-
At the concentration used (2 4 μM), the inhibitor suppressed the stimulatory effect of PMA but had no effect on exocytosis stimulated by forskolin
-
D Toullec et al . J. Biol. Chem 266, 15771 (1991). At the concentration used (2 4 μM), the inhibitor suppressed the stimulatory effect of PMA but had no effect on exocytosis stimulated by forskolin.
-
(1991)
J. Biol. Chem
, vol.266
, pp. 15771
-
-
Toullec, D.1
-
21
-
-
13344290799
-
-
note
-
2-], was measured in parallel with the electrophysiological recordings by dual wavelength microfluorimetry as described (17) with the use of fura-2 as the indicator. Before the measurements, the cells were loaded with the ester form (0.1 μM) of fura for 20 min.
-
-
-
-
22
-
-
0023009379
-
-
G Trube, T Ohno-Shosaku, P. Rorsman, Pfluegers Arch 407, 493 (1986); J Zunkler et al , Naunyn-Schmiedeberg's Arch Pharmacol 337, 225 (1988).
-
(1986)
Pfluegers Arch
, vol.407
, pp. 493
-
-
Trube, G.1
Ohno-Shosaku, T.2
Rorsman, P.3
-
25
-
-
0028789641
-
-
L. H. Philipson, Science 270, 1159 (1995); C F. Higgins, Cell 82, 693 (1995).
-
(1995)
Science
, vol.270
, pp. 1159
-
-
Philipson, L.H.1
-
26
-
-
0029164287
-
-
L. H. Philipson, Science 270, 1159 (1995); C F. Higgins, Cell 82, 693 (1995).
-
(1995)
Cell
, vol.82
, pp. 693
-
-
Higgins, C.F.1
-
27
-
-
13344265837
-
-
Mouse diabetic β cells are permanently depolarized even at subthreshold glucose concentrations [H P. Meissner and H. Schmidt, FEBS Lett. 67, 37 (1976)].
-
(1976)
FEBS Lett.
, vol.67
, pp. 37
-
-
Meissner, H.P.1
Schmidt, H.2
-
29
-
-
0028984692
-
-
K Bokvist et al , EMBO J 14 50 (1995)
-
(1995)
EMBO J
, vol.14
, pp. 50
-
-
Bokvist, K.1
-
30
-
-
13344293298
-
-
note
-
The phase angle was determined for each experiment. The absence of a change in cell conductance associated with the depolarizations indicates that the phase angle was correctly set and that the observed step changes of membrane capacitance are not attributable to variations of cell conductance.
-
-
-
-
32
-
-
13344290798
-
-
note
-
L E and E R contributed equally to this study and their names appear in alphabetical order. Supported by the Juvenile Diabetes Foundation International, the Swedish Medical Research Council, the Nordic Insulin Foundation Committee, National Institutes of Health, and the Swedish Diabetes Association.
-
-
-
|