Fujiwara K, Masuyama Y
Faculty of Pharmaceutical Sciences, Nagasaki University, Japan.
Histochem Cell Biol. 1995 Oct;104(4):309-16. doi: 10.1007/BF01464327.
We developed a mouse monoclonal antibody (ASPM-29, mAb) against spermine (Spm) conjugated to human serum albumin (HSA) using glutaraldehyde-sodium borohydride, for applications in immunocytochemistry (ICC). The antibody specificity was evaluated by an enzyme-linked immunosorbent assay (ELISA) binding test, simulating the ICC of tissue sections. ASPM-29 showed an almost equal immunoreactivity to Spm and spermidine (Spd) but no reactivity to any of the other polyamine (PA)-related compounds tested. By use of this antibody, indirect immunoperoxidase staining was observed in different tissues fixed with glutaraldehyde in combination with borohydride reduction. In contrast, immunoreactivity was quite low in tissues fixed only with glutaraldehyde. Absorption controls indicated that the immunostaining could be completely inhibited by 50 micrograms/ml of Spm or Spd and partially inhibited by N-acetylspermine (Ac-Spm), N1-acetylspermidine (N1-Ac-Spd), or N8-acetylspermidine (N8-Ac-Spd), but was hardly inhibited at all by other PA-related compounds or amino acids. The reactivity of the antibody with Spm conjugated on wells in an ELISA plate was inhibited by micromolar concentrations of Spm, Spd, Ac-Spm, N1-Ac-Spd, or N8-Ac-Spd, in decreasing order, but not by other small molecules. Dense ICC staining was observed in the paranuclear and basal cytoplasm of acinar cells of rat pancreas, submandibular gland and paratid gland, these results being in complete agreement with our recent ICC methods using other mAbs produced against N-(gamma-male-imidobutyryloxy) succinimide-conjugated Spm.
我们使用戊二醛-硼氢化钠制备了一种针对与人血清白蛋白(HSA)偶联的精胺(Spm)的小鼠单克隆抗体(ASPM-29,mAb),用于免疫细胞化学(ICC)。通过酶联免疫吸附测定(ELISA)结合试验评估抗体特异性,该试验模拟组织切片的ICC。ASPM-29对Spm和亚精胺(Spd)显示出几乎相同的免疫反应性,但对测试的任何其他多胺(PA)相关化合物均无反应性。使用该抗体,在戊二醛固定并结合硼氢化钠还原的不同组织中观察到间接免疫过氧化物酶染色。相比之下,仅用戊二醛固定的组织中免疫反应性相当低。吸收对照表明,免疫染色可被50微克/毫升的Spm或Spd完全抑制,并被N-乙酰精胺(Ac-Spm)、N1-乙酰亚精胺(N1-Ac-Spd)或N8-乙酰亚精胺(N8-Ac-Spd)部分抑制,但几乎不受其他PA相关化合物或氨基酸的抑制。ELISA板孔上偶联的Spm与该抗体的反应性被微摩尔浓度的Spm、Spd、Ac-Spm、N1-Ac-Spd或N8-Ac-Spd以递减顺序抑制,但不受其他小分子抑制。在大鼠胰腺、下颌下腺和腮腺腺泡细胞的核旁和基底细胞质中观察到密集的ICC染色,这些结果与我们最近使用针对N-(γ-马来酰亚胺丁酰氧基)琥珀酰亚胺偶联的Spm产生的其他mAb的ICC方法完全一致。