Laffafian I, Davies E V, Campbell A K, Hallett M B
University Department of Surgery, University of Wales College of Medicine, Cardiff, UK.
Cell Calcium. 1995 Apr;17(4):279-86. doi: 10.1016/0143-4160(95)90074-8.
The cytosolic free Ca2+ concentration in rat neutrophils was determined by ratiometric fluorometry and imaging of Fura-2. Transient elevations of cytosolic free Ca2+ concentration were provoked by addition of C9 to neutrophils pre-coated with C5b-8. The rate of rise of the cytosolic free Ca2+ concentration was dependent upon the concentration of C9. These changes in cytosolic free Ca2+ concentration occurred in the absence of cell lysis, since there was no release of Fura-2, and were the result of increased permeability to extracellular Ca2+. More than 96% of the rise in cytosolic free Ca2+ generation by C9 was dependent upon the presence of extracellular Ca2+, but did not occur via channels which were inhibited by the Ca2+ channel blocker SKF96365. The decrease in the permeability of the membrane to Ca2+ after C9 was not triggered by the rise in cytosolic free Ca2+. After attack by C9, individual neutrophils remained responsive to f-met-leu-phe, or further attack by C9, both producing Ca2+ transients. The recovery of the Ca2+ signal was consistent with the complement membrane attack complex generating a series of permeability thresholds in the plasma membrane. These data have implications for the understanding of the mechanisms underlying the inappropriate responsiveness of neutrophils at inflammatory sites.
通过Fura-2的比率荧光测定法和成像技术测定大鼠中性粒细胞胞质游离Ca2+浓度。向预先包被有C5b-8的中性粒细胞中添加C9可引发胞质游离Ca2+浓度的短暂升高。胞质游离Ca2+浓度的上升速率取决于C9的浓度。这些胞质游离Ca2+浓度的变化发生在细胞未裂解的情况下,因为没有Fura-2的释放,并且是细胞外Ca2+通透性增加的结果。C9引起的胞质游离Ca2+生成增加中超过96%依赖于细胞外Ca2+的存在,但不是通过被Ca2+通道阻滞剂SKF96365抑制的通道发生的。C9作用后膜对Ca2+通透性的降低不是由胞质游离Ca2+的升高触发的。C9攻击后,单个中性粒细胞对f-甲硫氨酰-亮氨酰-苯丙氨酸或C9的进一步攻击仍有反应,两者都会产生Ca2+瞬变。Ca2+信号的恢复与补体膜攻击复合物在质膜上产生一系列通透性阈值一致。这些数据对于理解炎症部位中性粒细胞不适当反应性的潜在机制具有重要意义。