Meuer S, Hugli T E, Andreatta R H, Hadding U, Bitter-Suermann D
Inflammation. 1981 Dec;5(4):263-73. doi: 10.1007/BF00911092.
Several anaphylatoxic substances (human C3a, guinea pig C3a, human C4a, guinea pig C5a, and a synthetic C3a-related hexapeptide) were compared with regard to their ability to induce secretion of [3H] serotonin from guinea pig platelets. Functional identity of the C3a preparations, C4a, and the hexapeptide was demonstrated by the phenomenon of crossed desensitization. Whereas C3a of human and guinea pig origin proved to be qualitatively and quantitatively identical, C4a expressed only 3% of the activity of the C3 fragments on a molar basis. Investigations with goat anti-guinea pig C3a demonstrate that human and guinea pig C3a possess one antigenic determinant in common; however, this determinant is not the C-terminal amino acid sequence. Addition of the anaphylatoxins with low doses of thrombin led to a potentiation of [3H] serotonin release from the platelets. Under these conditions C3a concentrations of 1.5 X 10(-10) mumol/liter (65 pg of C3a) could be detected. Thus the platelet system represents the most sensitive in vitro assay known for evaluation of biological activity of the C3a anaphylatoxins.
比较了几种过敏毒素物质(人C3a、豚鼠C3a、人C4a、豚鼠C5a以及一种合成的与C3a相关的六肽)诱导豚鼠血小板分泌[3H]血清素的能力。交叉脱敏现象证明了C3a制剂、C4a和六肽的功能同一性。虽然人和豚鼠来源的C3a在质量和数量上被证明是相同的,但C4a在摩尔基础上仅表现出C3片段活性的3%。用山羊抗豚鼠C3a进行的研究表明,人和豚鼠C3a有一个共同的抗原决定簇;然而,这个决定簇不是C末端氨基酸序列。低剂量凝血酶与过敏毒素的添加导致血小板释放[3H]血清素增强。在这些条件下,可以检测到1.5×10^(-10) μmol/升(65 pg C3a)的C3a浓度。因此,血小板系统是已知用于评估C3a过敏毒素生物活性的最敏感的体外测定方法。