Orange R P, Moore E G
J Immunol. 1976 Feb;116(2):392-7.
In the presence of L-cysteine, a selective and marked enhancement of the in vitro, immunologic release of slow reacting substance of anaphylaxis (SRS-A) from human peripheral leukocytes, sensitized monkey lung fragments, and sensitized guinea pig lung fragments was observed. In the rat, cysteine, but not sodium sulfide, enhanced the calcium ionophore (A23187)- induced release of SRS-A in vitro from mixed rat peritoneal cells and in vivo from the rat peritoneal cavity. Pretreatment of rats with cysteine also enhanced the IgGa-and anti-rat IgE-mediated release of SRS-A in vivo in the rat. These studies indicate a common biochemical mechanism involved in the formation and release of SRS-A from these different tissues and cells and further confirm the observation that the rat mast cell is not a major source of SRS-A in the rat.
在L-半胱氨酸存在的情况下,观察到从人外周血白细胞、致敏猴肺组织碎片和致敏豚鼠肺组织碎片中,过敏反应慢反应物质(SRS-A)的体外免疫释放有选择性且显著增强。在大鼠中,半胱氨酸而非硫化钠增强了钙离子载体(A23187)诱导的SRS-A从大鼠混合腹膜细胞的体外释放以及从大鼠腹腔的体内释放。用半胱氨酸对大鼠进行预处理也增强了大鼠体内IgGa和抗大鼠IgE介导的SRS-A释放。这些研究表明,在这些不同组织和细胞中SRS-A的形成和释放涉及一种共同的生化机制,并进一步证实了大鼠肥大细胞不是大鼠中SRS-A主要来源的观察结果。