期刊文献+

SIVmac239对猕猴B淋巴细胞增殖的抑制作用机制

Inhibition mechanism of SIVmac239 on macques B lymphocyte(MM133) proliferation in vitro
原文传递
导出
摘要 目的:探讨SIVmac239感染CD4+T淋巴细胞后,能否产生某些可抑制B淋巴细胞生长的活性因子,及其抑制作用的机制,为HIV/AIDS进一步的病原学研究和控制提供有益的线索。方法:用MTT实验观察不同时间收集的SIV-mac239感染的CD4+T淋巴细胞上清和未感染SIVmac239的CD4+T淋巴细胞的上清对猕猴B淋巴细胞生长的抑制作用,用3Hthymidine uptake assay判断这些上清是否抑制B淋巴细胞的DNA合成,用凝胶电泳方法检测DNA合成被抑制是否为凋亡的机制,用Western blot方法检测Cyclin D1的表达情况。结果:SIVmac239感染的CD4+T淋巴细胞上清含有抑制猕猴B淋巴细胞生长的因子,并且,其抑制效果随着作用时间的延长而增加。这些因子可较强的抑制CD4+T淋巴细胞的DNA合成,最高抑制率可达81%。凝胶试验结果未见DNA梯状条带。Western blot试验发现Cyclin D1表达被抑制。结论:SIVmac239感染CD4+T淋巴细胞可产生抑制B淋巴细胞生长的因子。此因子可较强的抑制猕猴B淋巴细胞DNA的合成,但并不引起B淋巴细胞凋亡。其主要机制为抑制猕猴B淋巴细胞的细胞周期蛋白D1的产生,使B淋巴细胞停止在G1期,即抑制作用的主要的机制为细胞被捕获在细胞周期的G1期。本研究结果发现一个新的现象,即猕猴B淋巴细胞虽然不被SIVmac239感染,但可被SIVmac239感染的CD4+T淋巴细胞产生的细胞因子所捕获,抑制其细胞DNA合成,从而可导致该细胞的功能发生障碍和影响机体体液免疫作用。 Objective: To explore the inhibition factors which CD4^+T lymphocyte secret after infection with SIVmac239, whether or not these factors can inhibit the B lymphocyte proliferation activity and it's inhibition mechanism, some helpful clue for pathogenology research of AIDS will be supplied, nehtods: Proliferation activity of MM133 cells treated by the supernatant of C8166 cells infected SIVmac239 tested by MTT assay. The inhibition of DNA synthesis of Supernatant of C8166 cells infected by SIVmac239 on B cells estimated by 3H thymidine uptake assay, whether or not the apoptosis happened when the DNA synthesis inhibiton judgeged by DNA fragmentation detection. Cyclin D1 expression was examined through western blot assay. Results: SIVmac239 can stimulate CD4^+T lymphocyte to secret some inhibitant factors for the macques B lymphocyte, these factors can inhibit the DNA synthesis of B cells through 3H thymidine uptake assay, electrophoresis result did not show DNA ladder,there is not Cy- clin D1 bands on western blot assay for the concentration of 25% and 12.5% supernantant of C8166 infected by SIVmac239. Conclusion:CD4^+T lymphocyte infected by SIVmac239 can produce some inhibitant factors on the macques B lymphocyte, these factors also can inhibit the DNA synthesis of B cells, but the factors did not induce the apoptosis of B cells, the major mechanism of inhibition of the factors on the B cells is to arrest the cells in G1 phase duing cell cycling. A new phenomenon has been found in this experiment, B cells can not be infected by SIVmac239, but they will be arrested in G1 phase by some factors produced by CD4^+T Lymphocyte infected with SIVmac239. Tus the function of B lymphocytes and the h umoral immunity may be limited.
出处 《中国卫生检验杂志》 CAS 2009年第6期1219-1221,共3页 Chinese Journal of Health Laboratory Technology
基金 黑龙江省教育厅科学技术研究项目(11511161)
关键词 SIVMAC239 CD4^+T淋巴细胞 B淋巴细胞 抑制机制 SIVmac239 CD4^+T Lymphocyte B Lymphocyte Inhibition mechanism
  • 相关文献

参考文献7

  • 1Reed LJ, J Muench. A simple method of estimating fifty percent endpoints[ J]. Am J Hyg, 1938, 27:493 -497.
  • 2Mosmann T. Rapid calorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays[ J ]. lmnmnol Methods,1983,65 : 55 -63.
  • 3Megumi Takahashi, Kozo Yokomuro. Mouse paraenchymal liver cells in culture secret a growth inhibitor for myeloma cells [ J ]. Hepatology, 1996,24:225 - 229.
  • 4Wyllie AH. Glucocorticoid - induced thymocyte apoptosis is associated with endogenous endonuclease activation [ J ]. Nature, 1980,254:555 - 556.
  • 5Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4 [ J ]. Nature, 1970,227 (259) :680 - 685.
  • 6Matsushime H, Quelle D, Shurtleff S, et al. D - type cyclin - dependent kinase activity in mammalian cells[ J]. Mol Cell Biol, 1994, 14: 2066 - 2076.
  • 7Meyerson M, Harlow E. Identification of G1 kinase activity for cdk6, a novel cyclin D partner[ J ]. Mol Cell Biol, 1994,14:2077 - 2086.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部