Torrens Y, Beaujouan J C, Saffroy M, Daguet de Montety M C, Bergström L, Glowinski J
Proc Natl Acad Sci U S A. 1986 Dec;83(23):9216-20. doi: 10.1073/pnas.83.23.9216.
Binding sites for substance P were labeled on intact cortical glial cells from newborn mice in primary culture using 125I-labeled Bolton-Hunter-labeled substance P. Maximal specific binding (95% of total binding) was reached after 2-3 weeks in culture. The binding was saturable, reversible, and temperature dependent. Scatchard and Hill analysis revealed a single population of noninteracting high-affinity binding sites (Kd, 0.33 nM; Bmax, 14.4 fmol per dish). Competition studies made with tachykinins and substance P analogues indicated that the characteristics of the 125I-labeled Bolton-Hunter labeled substance P binding sites on glial cells were identical to those on rat brain synaptosomes. 125I-labeled Bolton-Hunter labeled substance P binding sites were visualized by autoradiography, and differences in the intensity of labeling were seen among astrocytes. Substance P was found to stimulate phosphatidylinositol turnover; the EC50 value (0.36 nM) was identical to the IC50 value (0.38 nM) determined in binding studies. 125I-labeled Bolton-Hunter labeled substance P binding sites were also found on astrocytes derived from other brain structures and from the spinal cord of mice.
使用125I标记的博尔顿-亨特标记的P物质,在原代培养的新生小鼠完整皮质胶质细胞上标记P物质的结合位点。培养2 - 3周后达到最大特异性结合(占总结合的95%)。该结合具有饱和性、可逆性且依赖温度。斯卡查德分析和希尔分析显示存在单一群体的非相互作用高亲和力结合位点(解离常数Kd为0.33 nM;每培养皿的最大结合量Bmax为14.4 fmol)。用速激肽和P物质类似物进行的竞争研究表明,胶质细胞上125I标记的博尔顿-亨特标记的P物质结合位点的特征与大鼠脑突触体上的相同。通过放射自显影观察到125I标记的博尔顿-亨特标记的P物质结合位点,且在星形胶质细胞之间观察到标记强度的差异。发现P物质可刺激磷脂酰肌醇周转;其半数有效浓度(EC50值为0.36 nM)与结合研究中确定的半数抑制浓度(IC50值为0.38 nM)相同。在源自小鼠其他脑结构和脊髓的星形胶质细胞上也发现了125I标记的博尔顿-亨特标记的P物质结合位点。