FEBS Letters | |
Alamethicin channel permeation by Ca2+, Mn2+ and Ni2+ in bovine chromaffin cells | |
Garcia-Sancho, J.1  López, M.G.2  Fonteriz, R.I.1  Garcia, A.G.2  | |
[1] Departamento de Fisiologia y Bioquimica, Facultad de Medicina, Universidad de Valladolid, 47005-Valladolid, Spain;Departamento de Farmacologia y Terapèutica, Facultad de Medicina, Universidad Autonòma de Madrid, Arzobispo, Morcillo, 4, 28029-Madrid, Spain | |
关键词: Alamethicin; Calcium signal; Manganese; Nickel; Furu-2; Chromaffin cell; | |
DOI : 10.1016/0014-5793(91)80560-P | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
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【 摘 要 】
Alamethicin causes a concentration-dependent increase of (Ca2+), in suspensions of bovine adrenal chromaffin cells loaded with fura-2. The basal levels of Ca2+ (234 ± 37 nM; n=4) increased to a maximum of 2347±791 nM (n=3) with 100 μg/ml alamethicin. In the presence of 1 nM Ca2+ the increase reached a plateau within about 2–5 s. This increase was due to Ca2+ entry into chromaffin cells, since in the absence of Ca2+ alamethicin did not modify [Ca2+]. This contrasts with ionomycin (1 μM) which produced a Ca2+ transient even in the absence of Ca2+, Mn2+ ions also entered chromaffin cells in the presence of alamethicin, as measured by the quenching of fura-2-fluorescence following excitation at 360 nm. Resting chromaffin cells had a measurable permeability to Mn2+ which was drastically increased by cell depolarization by K+ (50 nM) addition. This suggests that Mn2+ is able to permeate voltage-dependent Ca2+ channels. Ni2+ uptake into either resting of K+-stimulated chromaffin cells was undetectable, but addition of alamethicin induced rapid uptake of this cation. The alamethicin-induced entry of Ni2+ was decreased by 50 mM K+. Overall, the results are compatible with the formation by alamethicin of ion channels in chromaffin cell plasma membranes.
【 授权许可】
Unknown
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