Okamoto M, Mayer M M
J Immunol. 1978 Jan;120(1):279-85.
In the previous paper it was suggested that the primary action of guinea pig lymphotoxin (LT) involved creation of ionic imbalances within the target L cells. The nature of these ionic disturbances is explored in this paper. The exogenous addition of CaCl2, but not KCl or NaCl, inhibited the cytotoxic action of LT. Cellular uptake rates of 45Ca++, but not 86Rb+, increased in LT-damaged L cells. The factor responsible for increasing the 45Ca++ uptake rate cochromatographed on a hydroxyapatite column with the cytotoxic activity of LT. Ouabain prevented the LT-mediated lysis and, concomitantly, depressed the LT-induced increase of 45Ca++ uptake rate. The LT-damaged L cells excluded trypan blue to the same extent as the normal cells. The addition of LT to and LT-resistant L cell mutant affected neither the 45Ca++ uptake rate nor the viability. From these observations, damage to the calcium transport system in the L cell plasma membrane is proposed as a mechanism of LT action.
在前一篇论文中曾提出,豚鼠淋巴毒素(LT)的主要作用涉及在靶L细胞内产生离子失衡。本文探讨了这些离子紊乱的性质。外源添加CaCl₂可抑制LT的细胞毒性作用,而添加KCl或NaCl则无此作用。在LT损伤的L细胞中,⁴⁵Ca²⁺的细胞摄取率增加,而⁸⁶Rb⁺的摄取率未增加。负责提高⁴⁵Ca²⁺摄取率的因子与LT的细胞毒性活性在羟基磷灰石柱上共层析。哇巴因可阻止LT介导的细胞裂解,并同时降低LT诱导的⁴⁵Ca²⁺摄取率增加。LT损伤的L细胞排斥锥虫蓝的程度与正常细胞相同。向LT抗性L细胞突变体中添加LT,既不影响⁴⁵Ca²⁺摄取率,也不影响细胞活力。根据这些观察结果,提出L细胞质膜中钙转运系统的损伤是LT作用的一种机制。