Expression of allograft inflammatory factor-1 in kidneys: A novel molecular component of podocyte
Author(s) -
Yutaka Tsubata,
Minoru Sakatsume,
Asa Ogawa,
Bassam Alchi,
Yoshikatsu Kaneko,
Takeshi Kuroda,
Hiroshi Kawachi,
Ichiei Narita,
Tadashi Yamamoto,
Fumitake Gejyo
Publication year - 2006
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/sj.ki.5001941
Subject(s) - podocyte , nephritis , immunoelectron microscopy , nephrosis , pathology , biology , kidney , glomerular basement membrane , renal glomerulus , immunohistochemistry , basement membrane , glomerulonephritis , nephropathy , microbiology and biotechnology , medicine , endocrinology , proteinuria , diabetes mellitus
Our comprehensive gene expression profiles of the kidneys in an anti-glomerular basement membrane (GBM) nephritis model using DNA arrays revealed that allograft inflammatory factor-1 (AIF-1) was one of the highly expressed genes. Here, we explored the pathological significance of AIF-1 expression in the kidneys. The expression pattern of AIF-1 mRNA and protein in the kidneys of normal and diseased rats, such as anti-GBM nephritis and puromycin aminonucleoside nephrosis, was investigated by in situ hybridization, immunohistochemistry, and immunoelectron microscopy. Furthermore, the expression of AIF-1 in human kidneys and urinary sediments was examined. AIF-1 was expressed at both mRNA and protein levels in podocytes of normal and diseased rats, and in infiltrating cells in anti-GBM nephritis kidneys. The expression of AIF-1 in podocytes was constitutive; positive in podocytes of both normal and diseased rats. In humans, AIF-1 was expressed in podocytes and infiltrating inflammatory cells, similarly. Moreover, it was detected in urinary podocytes from patients with immunoglobulin A nephropathy. These data document for the first time that AIF-1, a constitutively expressed protein in rat and human podocytes, is a novel molecular component of podocytes, and that the upregulation of AIF-1 in an anti-GBM nephritis model may mainly be a consequence of its expression in infiltrating cells.
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