Kream R M, Schoenfeld T A, Mancuso R, Clancy A N, el-Bermani W, Macrides F
Proc Natl Acad Sci U S A. 1985 Jul;82(14):4832-6. doi: 10.1073/pnas.82.14.4832.
Antisera generated to substance P-Gly (SP-G) and substance P-Gly-Lys (SP-G-K), the likely unamidated COOH-terminally extended forms of substance P, were used to quantify and localize substance P precursor forms in hamster brain stem and spinal cord. The precursor determinant SP-G-K was liberated from larger heterogeneous forms by mild trypsinization of tissue extracts and was converted into the second precursor determinant, SP-G, by subsequent treatment with carboxypeptidase B. The basal levels of SP-G-K in brain stem and spinal cord were approximately equal to 0.5 pg/mg of tissue and rose 43- to 64-fold after trypsinization. Basal levels of SP-G were comparable to those of SP-G-K and rose 10- to 29-fold after combined enzyme treatments. Immunohistochemical labeling of axons and somata with anti-SP-G-K increased dramatically after trypsinization. This labeling was eliminated by preadsorption with authentic SP-G-K but not substance P or SP-G. Gel-permeation chromatography revealed SP-G-K-like immunoreactivity in fractions corresponding to considerably higher molecular weight than mature substance P. Collectively, these results support the hypothesis that substance P is synthesized from larger precursors and demonstrate that extended precursor forms are normally present in the axons and somata of neural systems that synthesize substance P.
针对P物质-甘氨酸(SP-G)和P物质-甘氨酸-赖氨酸(SP-G-K)(可能是P物质未酰胺化的C末端延伸形式)产生的抗血清,用于定量和定位仓鼠脑干和脊髓中的P物质前体形式。通过对组织提取物进行温和的胰蛋白酶消化,前体决定簇SP-G-K从较大的异质形式中释放出来,并通过随后用羧肽酶B处理转化为第二个前体决定簇SP-G。脑干和脊髓中SP-G-K的基础水平约为0.5 pg/mg组织,胰蛋白酶消化后升高43至64倍。SP-G的基础水平与SP-G-K相当,联合酶处理后升高10至29倍。胰蛋白酶消化后,用抗SP-G-K对轴突和胞体进行免疫组织化学标记显著增加。这种标记通过用 authentic SP-G-K预吸附消除,但不能用P物质或SP-G消除。凝胶渗透色谱显示,在对应于比成熟P物质分子量高得多的级分中存在SP-G-K样免疫反应性。总的来说,这些结果支持P物质由较大前体合成的假设,并证明延伸的前体形式通常存在于合成P物质的神经系统的轴突和胞体中。