Exploring Mycobacterium tuberculosis infection-induced alterations in gene expression in macrophage by microarray hybridization

被引:0
|
作者
谢建平
李瑶
乐军
徐永忠
黄达蔷
梁莉
王洪海
机构
[1] Shanghai Pulmonary Hospital, Shanghai200433,China , Shanghai200433 , Shanghai200092,China , Shanghai200433,China
[2] State Key Laboratory of Genetic Engineering, Institute of Genetics, Schoolof Life Science, Fudan University,State Key Laboratory of Genetic Engineering, Institute of Genetics, Schoolof LifeScience, Fudan University,State Key Laboratory of Genetic Engineeri
[3] Institute of Modern Biopharmaceuticals, School of Life Science, Southwest China Normal University, Chongqing400715,China , Shanghai200433
[4] UnitedGene Holdings, Ltd, Shanghai 200092, China , Shanghai200433, China
关键词
macrophage U937; differential global gene profiling; Mycobacterium tuberculosis; cDNA microarray;
D O I
暂无
中图分类号
R521 [肺结核];
学科分类号
1002 ; 100201 ;
摘要
Tuberculosis remains a serious threat to public health. Its causative agent Mycobacte- rium tuberculosis is an intracellular pathogen which survives and replicates within cells of the host immune system, primarily macrophages. Knowledge of the bacteria-macrophage interaction can help to develop novel measures to combat the disease. The global gene expression of macro- phage following invasion by and growth of M. tuberculosis was studied by cDNA microarray. Of the 12800 human genes analyzed, totally 473 (3.7%) macrophage genes were differentially expressed after being infected by M. tuberculosis, among which, only 25 (5.2%, corresponding to less than 0.2% of the 12800 genes) genes were up-regulated, while others (94.8%) were down-regulated against the control. Of the 473 genes, 376 genes are registered in the GenBank, and 97 are novel genes. Expression of 5 up-regulated genes has been induced by more than 3-fold. 25 genes were down-regulated by more than 3-fold. Syndecan binding protein has been down-regu- lated up to 12.5-fold. The data gave an insight into the early gene expression in macrophage ensuing M. tuberculosis infection and a basis for further study.
引用
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页码:337 / 347 +449
页数:12
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