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Exploring Mycobacterium tuberculosis infection-induced alterations in gene expression in macrophage by microarray hybridization
Authors:XIE Jianping  LI Yao  YUE Jun     XU Yongzhong   HUANG Daqiang LIANG Li & WANG Honghai . State Key Laboratory of Genetic Engineering
Affiliation:XIE Jianping,LI Yao,YUE Jun 1,3,XU Yongzhong 1,HUANG Daqiang LIANG Li & WANG Honghai 1. State Key Laboratory of Genetic Engineering,Institute of Genetics,School of Life Science,Fudan University,Shanghai 200433,China, 2. Institute of Modern Biopharmaceuticals,School of Life Science,Southwest China Normal University,Chongqing 400715,China, 3. Shanghai Pulmonary Hospital,Shanghai 200433,China, 4. United Gene Holdings,Ltd.,Shanghai 200092,China
Abstract: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.
Keywords:macrophage U937   differential global gene profiling   Mycobacterium tuberculosis   cDNA microarray.
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