Rabovsky J, Goddard M, Pailes W H, Judy D J, Castranova V
National Institute for Occupational Safety and Health, Division of Respiratory Disease Studies, Morgantown, WV 26505.
Res Commun Chem Pathol Pharmacol. 1990 Aug;69(2):163-72.
Isolated rat alveolar macrophages aggregate in the presence of PAF in a dose- and cell-dependent manner. Saturation was achieved at 80 microM PAF. The response was increased linearly with cell number up to a concentration of 3 x 10(6) cells/ml, but decreased at higher cell concentrations. The stereoisomer, enantio-PAF, and the C2-acetyl hydrolyzed product, lyso-PAF, each caused aggregation of isolated rat alveolar macrophages in a manner similar to that for PAF. The PAF-induced aggregation of alveolar macrophages may be mediated through non-specific binding sites and may represent a toxic response to relatively high levels of PAF that released at localized sites.
分离出的大鼠肺泡巨噬细胞在血小板活化因子(PAF)存在的情况下,会以剂量和细胞依赖性方式聚集。在80微摩尔PAF时达到饱和。反应随细胞数量线性增加,直至浓度达到3×10⁶个细胞/毫升,但在更高细胞浓度时会下降。立体异构体对映体PAF和C2-乙酰水解产物溶血PAF,各自以类似于PAF的方式引起分离出的大鼠肺泡巨噬细胞聚集。PAF诱导的肺泡巨噬细胞聚集可能通过非特异性结合位点介导,并且可能代表对在局部位点释放的相对高水平PAF的毒性反应。