Meuer S, Zanker B, Hadding U, Bitter-Suermann D
J Exp Med. 1982 Mar 1;155(3):698-710. doi: 10.1084/jem.155.3.698.
The biologic activity of the anaphylatoxic peptides C5a and C3a is regulated efficiently at the target-cell level by the phenomenon of desensitization. Desensitization of platelets is stimulus specific and can be induced by low concentrations of anaphylatoxins without any preceding secretory event. In contrast to activation to secretion, desensitization is Ca++ independent but much more time consuming, especially at lower temperatures where both processes differ markedly in reaction velocity. This low zone desensitization insures that secretion from platelets only occurs when high amounts of anaphylatoxins are rapidly generated in the vicinity of the target-cell. Consequently, stimulus-specific unresponsiveness of the target cells can be induced by slowly increasing the concentration of the respective stimuli in their vicinity. Cellular control seems to act as a first-line mechanism of regulation, whereas the role of fluid-phase control is considered as preventing longer persistence and systemic accumulation of active anaphylatoxins.
过敏毒素肽C5a和C3a的生物活性通过脱敏现象在靶细胞水平上得到有效调节。血小板的脱敏具有刺激特异性,可由低浓度的过敏毒素诱导,且无需任何先前的分泌事件。与激活至分泌相反,脱敏不依赖Ca++,但耗时得多,尤其是在较低温度下,此时两个过程的反应速度有显著差异。这种低区脱敏确保血小板仅在靶细胞附近快速产生大量过敏毒素时才发生分泌。因此,通过缓慢增加其附近相应刺激物的浓度,可诱导靶细胞产生刺激特异性无反应性。细胞控制似乎作为一种一线调节机制,而液相控制的作用被认为是防止活性过敏毒素的持续时间延长和全身积累。