Overexpression of interferon-activated gene 202 (Ifi202) correlates with the progression of autoimmune glomerulonephritis associated with the MRL chromosome 1
Autor: | Nobuya Sasaki, Akihiro Kamikawa, Yoshiharu Hashimoto, Daiji Endoh, Yasuhiro Kon, Saori Otsuka, Osamu Ichii |
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Jazyk: | angličtina |
Rok vydání: | 2010 |
Předmět: |
Mice
Inbred MRL lpr kidney Lupus nephritis Congenic Thymus Gland Biology Autoimmune Diseases Mice Mice Congenic Glomerulonephritis Rheumatology Interferon medicine Animals Humans Genetic Predisposition to Disease Tissue Distribution Gene Ifi202 lupus nephritis Kidney Mice Inbred NZB Intracellular Signaling Peptides and Proteins Chromosome medicine.disease Chromosomes Mammalian MRL congenic mouse Mice Inbred C57BL medicine.anatomical_structure Gene Expression Regulation Immunology Disease Progression interferon activated gene 202 Spleen medicine.drug autoimmune glomerulonephritis |
Zdroj: | Lupus. 19(8):897-905 |
ISSN: | 0961-2033 |
Popis: | B6.MRLc1(82—100) congenic mice carrying the telomeric region of lupus-prone MRL chromosome 1 develop autoimmune glomerulonephritis (GN). The GN susceptibility locus of B6.MRLc1(82—100) contains the interferon activated gene 200 (Ifi200) family, which consists of Ifi202, 203, 204, and 205. Recently, Ifi202 was suggested as a candidate gene for murine lupus. In this study, we assessed the association between Ifi200 family and GN in several disease models. We compared the expression of Ifi200 family members in 24 organs between the C57BL/6 and B6.MRLc1(82-100). The expressions of Ifi200 family members differed between strains, and the most dramatic differences appeared in Ifi202 expression. Briefly, in the blood, immune organs, lungs, and testes mRNA expression was higher in B6.MRLc1(82—100) mice. In the kidney and immune organs, only Ifi202 expression increased with the development of GN in B6.MRLc1(82—100), and significant differences from C57BL/6 were observed even before disease onset. Ifi202 expression in the kidneys of BXSB, NZB/WF1, and MRL/lpr was also significantly high in the early- and late-disease stages. Furthermore, laser microdissection-reverse-transcriptase-polymerase chain reaction analysis confirmed the high Ifi202 expression in all areas of B6.MRLc1(82—100) kidneys. In conclusion, in the Ifi200 family, Ifi202 expressions in the kidney and immune organs significantly increased with GN progression. |
Databáze: | OpenAIRE |
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