Pellegrino M A, Ferrone S, Cooper N R, Dierich M P, Reisfeld R A
J Exp Med. 1974 Aug 1;140(2):578-90. doi: 10.1084/jem.140.2.578.
Cultured human lymphoid cells RPMI 8866 at different stages of their growth cycle vary in their susceptibility to lysis by rabbit, human, and guinea pig complement activated by HL-A antibodies or heterologous antibodies directed to membrane antigens; cells in G(1) phase are the least sensitive to lysis. To investigate the cause of differential susceptibility of cells RPMI 8866 to lysis, the expression of HL-A determinants and the ability of cells to react with complement were investigated. No change was detected in the density of HL-A antigens on RPMI 8866 cells in synchronous growth as determined by quantitative microabsorption assays, isotopic antiglobulin tests and yields of soluble HL-A antigens. Cells did not vary during the growth cycle in their ability to interact with complement components and in their capacity to activate the complement system through the classical or alternate pathway. These data suggest that variability in lytic susceptibility is due to changes in the structure of the cell membrane or in its ability to repair complement induced damage at certain intervals during the cell cycle. Therefore, this cell line constitutes a useful model to investigate the final steps of the cytolytic reaction.
处于不同生长周期阶段的培养人淋巴细胞RPMI 8866,对由HL - A抗体或针对膜抗原的异种抗体激活的兔、人及豚鼠补体的裂解敏感性各不相同;处于G(1)期的细胞对裂解最不敏感。为研究RPMI 8866细胞对裂解敏感性差异的原因,对HL - A决定簇的表达及细胞与补体反应的能力进行了研究。通过定量微量吸收测定、同位素抗球蛋白试验及可溶性HL - A抗原产量测定,未检测到同步生长的RPMI 8866细胞上HL - A抗原密度的变化。在生长周期中,细胞与补体成分相互作用的能力以及通过经典或替代途径激活补体系统的能力并无差异。这些数据表明,裂解敏感性的差异是由于细胞膜结构的变化或其在细胞周期的特定间隔修复补体诱导损伤的能力变化所致。因此,该细胞系构成了一个研究溶细胞反应最终步骤的有用模型。