Schloss P, Mayser W, Niehuis A, Betz H
Abteilung Neurochemie, Max-Planck-Institut für Hirnforschung, Frankfurt, Germany.
Biochem Biophys Res Commun. 1994 Mar 30;199(3):1320-5. doi: 10.1006/bbrc.1994.1375.
The acetylcholine precursor choline is transported into cholinergic neurons by a high-affinity, sodium-dependent mechanism that is selectively localized to the cholinergic nerve terminal. In addition, a low-affinity, sodium-independent choline uptake system is present in cholinergic and non-cholinergic cells which deliver choline for cell membrane anabolism. Here, we show that uptake of [3H]choline into cultured fibroblast cell lines exhibits high affinity (Km < or = 10 microM), is sodium-dependent, and is blocked by hemicholinium, a classical inhibitor of neuronal high-affinity choline uptake. Our data indicate that sodium-dependent high-affinity choline transport systems are also present in non-cholinergic cells.
乙酰胆碱前体胆碱通过一种高亲和力、依赖钠的机制转运进入胆碱能神经元,该机制选择性地定位于胆碱能神经末梢。此外,胆碱能和非胆碱能细胞中存在一种低亲和力、不依赖钠的胆碱摄取系统,该系统为细胞膜合成代谢提供胆碱。在此,我们表明,[3H]胆碱摄取到培养的成纤维细胞系中表现出高亲和力(Km≤10微摩尔),依赖钠,并被半胱氨酸阻断,半胱氨酸是神经元高亲和力胆碱摄取的经典抑制剂。我们的数据表明,非胆碱能细胞中也存在依赖钠的高亲和力胆碱转运系统。