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| Id: | 19916
| | Author: | Yogi, Yasuko; Nomaguchi, Hiroko; Sakamoto, Yoshiki; Matsuoka, Masanori; Fujimura, Takao; Okamura, Haruki; Hioki, Kyoji; Saito, Muneo; Nomura, Tatsuji. | | Title: | Cytokine gene expression in the foot pad and spleen of BALB/cAJcI mice infected with M. leprae.
| | Source: | Int. J. Lepr;65(1):80-89, Mar., 1997. ilus, tab.
| | Abstract: | The cytokine mRNAs expressed in the foot pads and spleens of BALB/cAJcl mice infected with Mycobacterium leprae were studied by the reverse transcriptase-polymerase chain reaction (RT-PCR) method using cytokine-specific primers for interleukin-1 alpha (IL-1 alpha), -2, -4, -6, -10, -12-(p40), gamma interferon (IFN-gamma), tumor necrosis factor-alpha (TNF-alpha), and TNF-beta, and then for CD4 and CD8 markers. The pattern of cytokine gene expression in the foot pad which supports M. leprae growth was different from the expression in the spleen which does not permit M. leprae multiplication in mice. Before BALB/cAjcl mice were infected with M. leprae, IL-1 alpha and TNF-beta mRNAs were expressed physiologically in the foot pad while all of the cytokine genes examined were expressed in the spleen. In the foot pads of mice inoculated with M. leprae, in addition to the physiological appearance of IL-1 alpha and TNF-beta mRNAs, these signals were intensified. TNF-alpha expression was induced by the infection. On the other hand, in the spleens of mice inoculated with M. leprae, CD4 mRNA expression disappeared on day 1 of the infection, which was accompanied by the reduced expression of IL-2, -4, -6, and -12 mRNAs. The recovery of CD4 mRNA expression at a latter stage was accompanied by a corresponding increase of the cytokine mRNA expression. It was suspected that these results might permit restricted growth of M. leprae in the foot pads of normal mice. Furthermore, our study suggests that tissue-specific, local, immunologic characteristics are important in M. leprae growth. (AU)^ien.
| | Descriptors: | Citocinas/bios
Citocinas/genet
Mycobacterium leprae/imunol
| | Location: | BR191.1 |
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