Using a cDNA microarray to study cellular gene expression altered by Mycobacterium tuberculosis

来源 :Chinese Medical Journal | 被引量 : 0次 | 上传用户:liongliong545
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Objective To examine the global effects of Mycobacterium tuberculosis ( M tuberculosis ) infection on macrophages Methods The gene expression profiling of macrophage U937, in response to infection with M tuberculosis H 37 R a, was monitored using a high density cDNA microarray Results M tuberculosis infection caused 463 differentially expressed genes, of which 366 genes are known genes registered in the Gene Bank These genes function in various cellular processes including intracellular signalling, cytoskeletal rearrangement, apoptosis, transcriptional regulation, cell surface receptors, cell mediated immunity as well as a variety of cellular metabolic pathways, and may play key roles in M tuberculosis infection and intracellular survival Conclusions M tuberculosis infection alters the expression of host cell genes, and these genes will provide a foundation for understanding the infection process of M tuberculosis The cDNA microarray is a powerful tool for studying pathogen host cell interaction Objective To examine the global effects of Mycobacterium tuberculosis (M tuberculosis) infection on macrophages Methods The gene expression profiling of macrophage U937, in response to infection with M tuberculosis H 37 R a, was monitored using a high density cDNA microarray Results M tuberculosis infection caused These genes function in various cellular processes including intracellular signaling, cytoskeletal rearrangement, apoptosis, transcriptional regulation, cell surface receptors, cell mediated immunity as well as a variety of cellular metabolic pathways, and may play key roles in M ​​tuberculosis infection and intracellular survival Conclusions M tuberculosis infection alters the expression of host cell genes, and these genes will provide a foundation for understanding the infection process of M tuberculosis The cDNA micro array is a powerful tool for studying pathogen host cell interaction
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