Wright S C, Weitzen M L, Kahle R, Granger G A, Bonavida B
J Immunol. 1983 May;130(5):2479-83.
This investigation has employed the "innocent bystander" type of experimental design to determine whether soluble cytotoxic factor(s) are released during interactions between human peripheral blood lymphocytes (PBL) and NK-sensitive target cells. PBL cocultured with NK-sensitive Molt-4 or K562 target cells in the lower well of a miniaturized Marbrook culture released natural killer cytotoxic factors (NKCF), which diffused across a 0.2-mu Nucleopore membrane and lysed Molt-4 or K562 target cells cultured in the upper chamber. Coculture of PBL with the NK-resistant Raji or WI-L2 cell lines also induced release of NKCF. These factors were selectively cytotoxic to NK-sensitive targets and lysed Molt-4 and, to a lesser extent, K562 cells. However, Raji, WI-L2, and RPMI 1788 cells were all resistant to lysis. In addition, low density fractions from Percoll density gradients that were enriched for NK effector cells also released increased levels of NKCF during coculture with Molt-4 cells. Lysis of Molt-4 and K562 targets was observed after exposure to NKCF for 48 hr and 60 to 70 hr, respectively. Cellfree supernatants containing NKCF were obtained after a short time of incubation (i.e., within 5 hr of coculture of PBL with NK target cells). The factors were nondialyzable, stable at 56 degrees C for 3 hr, and showed partial loss of activity on storage at 4 degrees C or -20 degrees C for 7 days. These data suggest that NKCF may be involved in the lytic mechanism of human NK cell-mediated cytotoxicity.
本研究采用了“无辜旁观者”类型的实验设计,以确定在人外周血淋巴细胞(PBL)与NK敏感靶细胞相互作用期间是否会释放可溶性细胞毒性因子。在小型化的马尔布鲁克培养体系的下层孔中,将PBL与NK敏感的Molt-4或K562靶细胞共培养,释放出自然杀伤细胞毒性因子(NKCF),这些因子扩散穿过0.2μm的核孔膜,裂解在上层培养的Molt-4或K562靶细胞。PBL与NK抗性的Raji或WI-L2细胞系共培养也诱导了NKCF的释放。这些因子对NK敏感靶细胞具有选择性细胞毒性,可裂解Molt-4细胞,对K562细胞的裂解作用较弱。然而,Raji、WI-L2和RPMI 1788细胞均对裂解具有抗性。此外,Percoll密度梯度中富含NK效应细胞的低密度组分在与Molt-4细胞共培养期间也释放出更高水平的NKCF。分别在暴露于NKCF 48小时和60至70小时后观察到Molt-4和K562靶细胞的裂解。在短时间孵育后(即PBL与NK靶细胞共培养5小时内)获得了含有NKCF的无细胞上清液。这些因子不可透析,在56℃下3小时稳定,在4℃或-20℃下储存7天活性部分丧失。这些数据表明NKCF可能参与了人NK细胞介导的细胞毒性的裂解机制。