›› 2004, Vol. 24 ›› Issue (1): 34-36.

• 论文 • 上一篇    下一篇

小鼠骨髓前体细胞来源的树突状细胞超微结构

  

  1. 1.苏州大学基础医学系电镜室,苏州 215007;2.苏州大学生物技术研究所,苏州 215007
  • 收稿日期:2003-07-10 出版日期:2004-01-25 发布日期:2013-03-19

Ultrastructure of Murine Bone Marrow-derived Dendritic Cells

  1. 1.Darpartment of Electron Microscope,Medical School of Soochow University,2.Medical Biotech Institute,Life Sciences School of Soochow University, Suzhou 215007,China
  • Received:2003-07-10 Online:2004-01-25 Published:2013-03-19

摘要: 无菌制备BALB/c小鼠骨髓细胞,按常规方法分离纯化出树突状细胞(DCs),采用GM-CSF和IL-4诱导后,以凋亡肿瘤细胞负载未成熟DCs,再分别加入mCD40L-CHO细胞和TNF-α继续培养48h,按常规方法分别制备各发育阶段DCs的超薄切片。用透射电镜观察小鼠DCs在不同发育阶段的超微结构特征,并比较凋亡肿瘤细胞负载的小鼠DCs被CD40L和TNF-α刺激后超微结构的差别。实验结果证实DCs在分化发育成熟中存在异质性;DCs可通过吞噬凋亡的肿瘤细胞负载抗原;CD40配基化对DCs的分化成熟作用优于TNF-α。

关键词: 树突状细胞, 超微结构, 抗原负载, CD40

Abstract: Dentritic cells(DCs)and their progenitors from murine bone marrow were collected and induced in vitro by both granulocyte-macrophage colony-stimulating (GM-CSF) and interleukin-4 (11,4) for 5?6 days. Immature DCs were loaded with apoptotic tumor cells (AP-DC),then AP-DC vaccines were induced further maturation stimulated with MCD40L-CHO cells and TNF-arespectively for 48 h. These DCs’ morphology was observed under transmission electron micro-scropy. We found that immature DCs showed a few short and blunt cytoplasmic processes,there were specific morphology granules which liked earphone in some cells;the immature DCs had a powerful ability to capture antigens from apoptotic tumor cells in 5-6 th culturing day,the DCs engulfing the apoptotic bodies were observed; sub-cellular structures between CD40 ligation and TNF-astimulated DCs were different, the former had typical morphology of DCs which exhibited many dendritic protrusions and the nucleus was irregular in shape,the cytoplasm contained numerous mitochondria, ribosomes,well-developed Golgi complexes, but scantly lysosomes. In addition,DCs might be in contact with each other. The results suggested that DCs were heterogeneous;DCs can acquire antigen by phagocytosing apoptotic bodies ;CD40 ligation and the associated signal transduction played an essential role in myeloid DCs differentiation and maturation.

Key words: Dendritic cells, Ultrastructure, CD40, Loading antigen