Mycobacterium tuberculosis is capable of growing and survival within macrophage. The purpose of this study was to identify the genes regulated by infection of mycobacteria in human monocytic THP-1 cells. We used the differential display reverse transcriptase polymerase chain reaction (DD RT-PCR) and nothern blot analysis to confirm the differentially expressed genes from THP-1 cells infected with live Mycobacterium tuberculosis H37Rv, heat-kille Mycobacterium tuberculosis H37Rv and live Mycobacterium bovis BCG. Among many up or down-regulated clones, 27 clones were sequenced and compared with known genes on GenBank. Thirteen of over-expressed clones from THP-1 cells infected with live Mycobacterium tuberculosis H37Rv were identical to human prothymosin alpha, eight were novel clones and six clones showed homology with Human ferritin H chain, Escherichia coli bgl, Mouse RNA-dependent EIF-2 alpha kinase, E. coli htrL, Hyaluronan receptor and T cell receptor. Our result suggests that Mycobacterium tuberculosis might regulate prothymosin alpha gene transcription in monocytic THP-1 cell.
Animals ; Antigens, CD44 ; Clone Cells ; Databases, Nucleic Acid ; Escherichia coli ; Eukaryotic Initiation Factor-2 ; Ferritins ; Humans ; Macrophages ; Mice ; Mycobacterium bovis ; Mycobacterium tuberculosis* ; Mycobacterium* ; Phosphotransferases ; Receptors, Antigen, T-Cell ; Reverse Transcriptase Polymerase Chain Reaction ; Up-Regulation*