Bernheim J L, Dorian R E, Mendelsohn J
J Immunol. 1978 Mar;120(3):955-62.
The response of human lymphocytes to phytohemagglutinin (PHA) stimulation was assessed in detailed kinetic studies, in order to define conditions permitting and regulating proliferation. By utilizing live and dead cell counts, cell cycle characterizations, and calculations of rates of entry into S phase and mitosis, it was demonstrated that dilute culture conditions (2 X 10(5) cells/ml) enable lymphocytes to proliferate for a period of 5 or 6 days. Although cell division occurs in concentrated cultures (2 X 10(6) cells/ml), net proliferation is not demonstrable due to extensive cell death and earlier decay in the proliferative response. It is projected that without cell death the cell count would rise more than 6-fold in a dilute culture and 2-fold in a concentrated culture under these growth conditions. The kinetic analyses did not demonstrate separate PHA dose thresholds for blastogenesis and entry into S phase. High doses of PHA stimulated a suboptimal response by causing excessive cell death without reducing initial entry into the cell cycle. These results provide a kinetic explanation for the frequent observation of little net proliferation despite substantial 3H-thymidine incorporation in PHA-stimulated lymphocyte cultures. Cell death is identified as a parameter that must be considered in the interpretation of in vitro lymphocyte stimulation studies, and methods for quantifying the role of cell death are demonstrated.
为了确定允许和调节增殖的条件,在详细的动力学研究中评估了人淋巴细胞对植物血凝素(PHA)刺激的反应。通过利用活细胞和死细胞计数、细胞周期特征分析以及进入S期和有丝分裂速率的计算,结果表明,稀释培养条件(2×10⁵个细胞/毫升)可使淋巴细胞增殖5或6天。尽管在浓缩培养物(2×10⁶个细胞/毫升)中会发生细胞分裂,但由于广泛的细胞死亡和增殖反应的早期衰退,无法证明有净增殖。据推测,在这些生长条件下,若无细胞死亡,稀释培养物中的细胞计数将增加6倍以上,浓缩培养物中的细胞计数将增加2倍。动力学分析未显示出用于细胞增殖和进入S期的PHA剂量阈值存在差异。高剂量的PHA会导致过度的细胞死亡,从而刺激次优反应,而不会减少最初进入细胞周期的比例。这些结果为经常观察到的现象提供了动力学解释,即在PHA刺激的淋巴细胞培养物中,尽管有大量的³H-胸腺嘧啶核苷掺入,但净增殖却很少。细胞死亡被确定为在解释体外淋巴细胞刺激研究时必须考虑的一个参数,并展示了量化细胞死亡作用的方法。