Valchár M, Hanbauer I
Laboratory of Chemical Pharmacology, NHLBI, Bethesda, MD 20892, USA.
Mol Neurobiol. 1995 Aug-Dec;11(1-3):111-9. doi: 10.1007/BF02740689.
Ventral mesencephalic neurons contained only low-affinity and sodium-independent binding sites of [3H]WIN 35,428 (marker of dopamine transporter) during the first 10 d in primary cultures. These sites were present in cytosol, and they are not very probably related to dopamine transporter. After 12 d in culture, membrane-bound, high-affinity, and sodium-dependent [3H]WIN 35,428 binding sites were detected. In membranes prepared from cells 14 d in culture, cocaine displaced [3H]WIN 35,428 binding with similar potency to that in striatal membranes of adult rat brain. The high-affinity [3H]WIN 35,428 binding sites in mesencephalic neuronal cell cultures are very probably related to dopamine transporter. The development of high-affinity [3H]WIN 35,428 binding sites in neurons cultured for different time periods could be a useful model of dopamine transporter ontogenesis.
在原代培养的前10天,腹侧中脑神经元仅含有低亲和力且不依赖钠的[3H]WIN 35,428(多巴胺转运体标记物)结合位点。这些位点存在于胞质溶胶中,它们很可能与多巴胺转运体无关。培养12天后,检测到膜结合的、高亲和力且依赖钠的[3H]WIN 35,428结合位点。在培养14天的细胞制备的膜中,可卡因取代[3H]WIN 35,428结合的效力与成年大鼠脑纹状体膜中的相似。中脑神经元细胞培养物中的高亲和力[3H]WIN 35,428结合位点很可能与多巴胺转运体有关。在不同时间段培养的神经元中高亲和力[3H]WIN 35,428结合位点的发育可能是多巴胺转运体个体发生的一个有用模型。