期刊文献+

胸腺增龄性萎缩分子机制研究进展 被引量:4

Progress in study on the Molecular mechanism of age-related thymic involution
原文传递
导出
摘要 胸腺是哺乳动物重要的中枢免疫器官,是决定和制约免疫系统老化的关键。胸腺作为T细胞分化、发育、成熟重要场所,随着增龄表现出明显萎缩的现象进而影响到T细胞的发育、增殖和输出,从而造成外周淋巴组织中T细胞的质与量的异常,这样就不可避免地降低了免疫系统对外来的抗原应答性,导致病原体清除延迟,增加了老年人罹患癌症、自身免疫性疾病以及病毒、细菌等病原感染的风险,了解胸腺增龄性萎缩过程中转录因子、细胞因子的作用及增龄性萎缩胸腺功能恢复调节研究概况很有必要。 The thymus is the most important central immune organ of mammals which determines the aging of immune system.It is the major site of T cell maturation where extensive proliferation and differentiation occur.Age-related deterioration of the thymus can affect the function of peripheral T ceils,which inevitably impairs the responsiveness of immune system to foreign antigens,leading to delayed clearance of pathogens.This also increases the risk of elderly people suffering from cancer,autoimmune diseases and infections diseases caused by viruses,bacteria and other pathogens.This review presents the latest information on the role of transcription factors and cytokines in the progress of age-related thymic involution.We also review the studies on the regulation of the functional recovery of thymus.
作者 王长山 李丽 朱喜科 WANG Chang-shan;LI li;ZHU Xi-ke(Research Center for Medicine,China Medical Universiry the Shenging Hopital,Shenyang 110004,China)
出处 《国际免疫学杂志》 CAS 北大核心 2011年第4期257-261,共5页 International Journal of Immunology
基金 国家自然基金资助项目(30872715) 辽宁省自然科学基金项目(20082082)
关键词 胸腺增龄性萎缩 胸腺微环境 细胞因子 分子机制 Age-related thymic involution Thymie microenvironnlent Cytokines Molecular mechanism
  • 相关文献

参考文献39

  • 1Aspinall R, Pitts D, Lapenna A, et al. Immunity in the elderly: the role of the thymus. J Comp Pathol,2010,142 Suppl 1 : S111- 115.
  • 2Holl/inder GA, Krenger W, Blazar BR. Emerging strategies to boost thymie function. Curr Opin Pharmacol, 2010,10(4) :443- 453.
  • 3Hannestad J, Monjil DF, Diaz-Esnal B, et al. Age-dependent changes in the nervous and endocrine control of the thymus. Mi- erosc ltes Tech, 2004, 63(2) :94-101.
  • 4Chen BJ, Cui X, Sempowski GD, et al. Growth hormone acceler- ates immune recovery following allogeneic T-cell-depleted bonemarrow transplantation in mice. Exp Hematol, 2003, 31( 10): 953-958.
  • 5Morrhaye G, Kermani H, Legros J J, et al. Impact of growth hor- mone (GH) deficiency and GH replacement upon thymus function in adult patients. PLoS One, 2009, 4(5) :e5668.
  • 6Dudakov JA, Goldberg GL, Reiseger JJ, et al. Withdrawal of sex steroids reverses age- and chemotherapy-related defects in bone marrow lymphopoiesis. J Immunol, 2009, 182 (10) :6247-6260.
  • 7Gui J, Zhu X, Dohkan J, et al. The aged thymus shows normal recruitment of lymphohematopoietic progenitors but has defects in thymie epithelial cells. Int Immunol, 2007,19(10) :1201-1211.
  • 8Aspinall R, Andrew D, Age-associated thymic atrophy is not asso- ciated With a deficiency in the CD44 + CD25- CD3- CD4- CD8- thymocytes population. Cell Immunol, 2001,212(2) :150-157.
  • 9Schwarz BA, Sambandam A, Maillard I, et al. Selective thymus settling regulated by eytokine and chemokine receptors. J Immu- nol, 2007,178(4) :2008-2017.
  • 10Zhu X, Gui J, Dohkan J, et al. Lymphohematopoietie progenitors do not have a synchronized defect with age-related thymie involu- tion. Aging Cell, 2007,6 ( 5 ) :663-672.

同被引文献75

引证文献4

二级引证文献14

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