Chain B M, Kay P M, Feldmann M
Immunology. 1986 Jun;58(2):271-6.
The response of primed T cells to keyhole limpet haemocyanin (KLH) was used to compare the characteristics of antigen presentation by lymphoid dendritic cells, splenic and peritoneal macrophages. In a similar manner to macrophages, purified dendritic cells could be pulsed with antigen and subsequently fixed by brief glutaraldehyde fixation and still retain antigen presenting activity. Also, as previously reported for macrophages, presentation could be inhibited by chloroquine. These functional experiments suggested that the pathway of antigen presentation in dendritic cells and macrophages was similar or identical. However, biochemical studies, using radiolabelled antigen, showed that dendritic cells do not significantly degrade large proteins such as KLH to TCA-soluble form, but partially hydrolyse them to smaller peptide fragments. The significance of these results in terms of a model of the cellular pathways of antigen presentation is discussed.
用致敏T细胞对钥孔戚血蓝蛋白(KLH)的反应来比较淋巴树突状细胞、脾脏巨噬细胞和腹膜巨噬细胞的抗原呈递特性。与巨噬细胞类似,纯化的树突状细胞可用抗原脉冲处理,随后通过短暂的戊二醛固定进行固定,并且仍保留抗原呈递活性。此外,正如之前关于巨噬细胞的报道,氯喹可抑制呈递。这些功能实验表明,树突状细胞和巨噬细胞中的抗原呈递途径相似或相同。然而,使用放射性标记抗原的生化研究表明,树突状细胞不会将诸如KLH之类的大蛋白显著降解为三氯乙酸可溶性形式,而是将它们部分水解为较小的肽片段。本文讨论了这些结果在抗原呈递细胞途径模型方面的意义。