Hogan R J, Taylor W R, Cuchens M A, Naftel J P, Clem L W, Miller N W, Chinchar V G
Department of Microbiology, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Cell Immunol. 1999 Aug 1;195(2):110-8. doi: 10.1006/cimm.1999.1523.
This study examines cytotoxic mechanisms used by channel catfish peripheral blood-derived effector cells. Transmission electron microscopy (TEM), coupled with [(3)H]thymidine DNA fragmentation (JAM) and terminal deoxynucleotidyl nick-end labeling (TUNEL) assays, provided the first evidence that catfish peripheral blood cytotoxic effectors killed allogeneic targets via an apoptotic pathway. TEM demonstrated that the effector cell population present within peripheral blood leukocytes (PBLs) was composed of agranular lymphocytes that formed conjugates with, and induced apoptosis in, allogeneic target cells. Both JAM and TUNEL assays showed that PBLs induced target cell DNA fragmentation within 1 h of coculture. In addition, fixed effectors did not induce target cell necrosis or apoptosis, and target cell lysis was completely inhibited by chelation of free Ca(2+) by EGTA. These results suggest that catfish peripheral blood-derived effector cells utilize a secretory mechanism rather than a ligand-based mechanism to trigger apoptosis.
本研究考察了斑点叉尾鮰外周血来源的效应细胞所使用的细胞毒性机制。透射电子显微镜(TEM),结合[³H]胸腺嘧啶核苷DNA片段化(JAM)和末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)分析,首次提供了斑点叉尾鮰外周血细胞毒性效应细胞通过凋亡途径杀死同种异体靶细胞的证据。TEM显示,外周血白细胞(PBL)中的效应细胞群体由无颗粒淋巴细胞组成,这些细胞与同种异体靶细胞形成共轭物并诱导其凋亡。JAM和TUNEL分析均显示,共培养1小时内PBL诱导靶细胞DNA片段化。此外,固定的效应细胞不会诱导靶细胞坏死或凋亡,并且通过EGTA螯合游离Ca²⁺可完全抑制靶细胞裂解。这些结果表明,斑点叉尾鮰外周血来源的效应细胞利用分泌机制而非基于配体的机制来触发凋亡。