作者: LeslieC. McKinney , ElaineK. Gallin
DOI: 10.1007/BF00240483
关键词: Apamin 、 Pertussis toxin 、 Extracellular 、 Biophysics 、 Cholera toxin 、 Charybdotoxin 、 Biochemistry 、 Chemistry 、 Hyperpolarization (biology) 、 Patch clamp 、 Intracellular
摘要: The whole-cell patch clamp technique was used to test whether intracellular application of G-protein activators affect ionic currents in murine macrophages. Both the J774.1 macrophage-like cell line and primary bone marrow derived macrophages were used. Cells bathed Na Hanks' solution intracellularly dialyzed (via pipette) with K Hanks (145mm KCl, 1mm), kinetics (no time-dependent inactivation). Intracellular GTP (500 μm), GDP cAMP (100 μm+0.5mm ATP), or IP3 (20 μm) did not induce current; 100 μm ATPγS activated a half-maximal amount current. Induction outward current by 10 GTPγS could be prevented pre-exposing cells pertussis toxin but cholera toxin. This is selective since (i) its induction accompanied hyperpolarization toward EK, even after Kir had “washed out”, (ii) it present >90% both extracellular Cl replaced isethionate, (iii) induced conductance absent when Ki completely Cs, reduced approximately 1/3 [K]i 1/3. Quinidine (1mm) 4-aminopyridine (10mm) inhibited current, apamin (1 charybdotoxin not.