Goldsmith H L, Bell D N, Braovac S, Steinberg A, McIntosh F
McGill University Medical Clinic, Montreal General Hospital, Canada.
Biophys J. 1995 Oct;69(4):1584-95. doi: 10.1016/S0006-3495(95)80031-7.
Both chemical and physical effects of red cells have been implicated in the spontaneous aggregation of platelets in sheared whole blood (WB). To determine whether the chemical effect is due to ADP leaking from the red cells, a previously described technique for measuring the concentration and size of single platelets and aggregates was used to study the shear-induced aggregation of platelets in WB flowing through 1.19-mm-diameter polyethylene tubing in the presence and absence of the ADP scavenger enzyme system phosphocreatine-creatine phosphokinase (CP-CPK). Significant spontaneous aggregation was observed at mean tube shear rates, (G) = 41.9 and 335 s-1 (42% and 13% decrease in single platelets after a mean transit time (t) = 43 s, compared to 89 and 95% decrease with 0.2 microM ADP). The addition of CP-CPK, either at the time of, or 30 min before each run, completely abolished aggregation. In the presence of 0.2 microM ADP, CP-CPK caused a reversal of aggregation at (t) = 17 s after 30% of single cells had aggregated. To determine whether red cells exert a physical effect by increasing the time of interaction of two colliding platelets (thereby increasing the proportion of collisions resulting in the formation of aggregates), an optically transparent suspension of 40% reconstituted red cell ghosts in serum containing 2.5-micron-diameter latex spheres (3 x 10(5)/microliters) flowing through 100-microns-diameter tubes was used as a model of platelets in blood, and the results were compared with those obtained in a control suspension of latex spheres in serum alone. Two-body collisions between microspheres in the interior of the flowing ghost cell or serum suspensions at shear rates from 5 to 90 s-1 were recorded on cine film. The films were subsequently analyzed, and the measured doublet lifetime, tau meas, was compared with that predicted by theory in the absence of interactions with other particles, tau theor. The mean (tau meas/tau theor) for doublets in ghost cell suspensions was 1.614 +/- 1.795 (SD; n = 320), compared to a value of 1.001 +/- 0.312 (n = 90) for doublets in serum. Whereas 11% of doublets in ghost cell suspensions had lifetimes from 2.5 to 5 times greater than predicted, in serum, no doublets had lifetimes greater than 1.91 times that predicted. There was no statistically significant correlation between tau meas/tau theor and shear rate, but the values of tau meas/tau theor for low-angle collisions in ghost cell suspensions were significantly greater than for high-angle collisions.
红细胞的化学和物理效应均与剪切全血(WB)中血小板的自发聚集有关。为了确定化学效应是否是由于红细胞释放的ADP所致,采用一种先前描述的测量单个血小板和聚集体浓度及大小的技术,研究了在存在和不存在ADP清除酶系统磷酸肌酸 - 肌酸磷酸激酶(CP - CPK)的情况下,WB流经直径1.19毫米的聚乙烯管时血小板的剪切诱导聚集。在平均管剪切速率(G)= 41.9和335 s-1时观察到显著的自发聚集(平均通过时间(t)= 43 s后,单个血小板减少42%和13%,相比之下,0.2 microM ADP时减少89%和95%)。在每次运行时或运行前30分钟添加CP - CPK,可完全消除聚集。在存在0.2 microM ADP的情况下,CP - CPK在30%的单个细胞聚集后,于(t)= 17 s时导致聚集逆转。为了确定红细胞是否通过增加两个碰撞血小板的相互作用时间(从而增加导致聚集体形成的碰撞比例)来发挥物理效应,使用了一种光学透明的悬浮液,其中40%的重构红细胞膜泡存在于含有直径2.5微米乳胶球(3×10(5)/微升)的血清中,流经直径100微米的管子,以此作为血液中血小板的模型,并将结果与仅在血清中的乳胶球对照悬浮液所获得的结果进行比较。在剪切速率为5至90 s-1的情况下,用电影胶片记录流动的膜泡细胞或血清悬浮液内部微球之间的双体碰撞。随后对胶片进行分析,并将测量的双体寿命τmeas与在不存在与其他颗粒相互作用时理论预测的寿命τtheor进行比较。膜泡细胞悬浮液中双体的平均(τmeas/τtheor)为1.614±1.795(标准差;n = 320),而血清中双体的值为1.001±0.312(n = 90)。膜泡细胞悬浮液中11%的双体寿命比预测值大2.5至5倍,而在血清中,没有双体寿命大于预测值的1.91倍。τmeas/τtheor与剪切速率之间无统计学显著相关性,但膜泡细胞悬浮液中低角度碰撞的τmeas/τtheor值显著大于高角度碰撞的值。