Conroy M C, Orange R P, Lichtenstein L M
J Immunol. 1976 Jun;116(6):1677-81.
The ability of the calcium ionophore A23187 to release slow reacting substance of anaphylaxis (SRA-A) from human leukocytes was studied. About 25 times more SRS-A activity was released from aliquots of leukocytes by ionophore stimulation than by antigen stimulation, although comparable amounts of histamine were released. Cell separation studies revealed that granulocytes other than basophils were also capable of releasing SRS-A. The contractile activity released after challenge with ionophore appeared physicochemically identical to the SRS-A of rat or human origin released by antigen challenge in terms of its stability to base hydrolysis, inactivation by arylsulfatase, and chromatographic behavior on silicic acid and Sephadex LH-20 columns. We suggest that some mediators of allergic reactions previously associated, in man, only with antigen-IgE antibody interaction on mast cells or basophils may be released by other stimuli and from other cell types.
研究了钙离子载体A23187从人白细胞中释放过敏反应慢反应物质(SRA-A)的能力。尽管组胺释放量相当,但离子载体刺激白细胞等分试样释放的SRS-A活性比抗原刺激释放的活性高约25倍。细胞分离研究表明,除嗜碱性粒细胞外,粒细胞也能够释放SRS-A。离子载体激发后释放的收缩活性,在对碱水解的稳定性、芳基硫酸酯酶的失活作用以及在硅酸和Sephadex LH-20柱上的色谱行为方面,在物理化学性质上与抗原激发释放的大鼠或人源性SRS-A相同。我们认为,以前在人类中仅与肥大细胞或嗜碱性粒细胞上的抗原-IgE抗体相互作用相关的一些过敏反应介质,可能会由其他刺激从其他细胞类型中释放出来。