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Schroll, A; Eller, K; Huber, JM; Theurl, IM; Wolf, AM; Weiss, G; Rosenkranz, AR.
Tim3 is upregulated and protective in nephrotoxic serum nephritis.
Am J Pathol. 2010; 176(4):1716-1724 Doi: 10.2353/ajpath.2010.090859 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Rosenkranz Alexander
Co-Autor*innen der Med Uni Graz
Eller Kathrin
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Abstract:
T cell immunoglobulin and mucin protein-3 (Tim3) is mainly expressed on the cell surface of T-helper lymphocytes (T(H)) that negatively regulates T(H)-type 1 (T(H)-1) responses. Because blockade of Tim3 aggravates disease activity in T(H)-1-dependent diseases, we investigated whether Tim3 is involved in the pathogenesis of the T(H)-1-dependent nephrotoxic nephritis (NTS). We first evaluated Tim3 expression in mice after induction of nephrotoxic serum nephritis (NTS) and then studied the effects of anti-Tim3 treatment toward the course of NTS for up to seven days. Whereas Tim3 expression was undetectable in control mice, we found significantly increased Tim3 expression in kidneys, but not in draining lymph nodes, at one, four, and eight weeks after induction of NTS. Tim3-expressing cells that infiltrated kidneys of mice subjected to NTS turned out to be CD4(+) T cells rather than CD8(+) cytotoxic T cells and dendritic cells. Administration of a blocking anti-Tim3 antibody aggravated nephritis as shown by significantly increased albuminuria, respective histological changes, and increased expression of the kidney injury molecule lipocalin-2. In parallel, an increase of infiltrating T cells, macrophages, and macrophage pro-inflammatory cytokine formation as well as increased proliferation and apoptosis in kidneys of anti-Tim3-treated mice was detected. Together, we provide the first evidence that Tim3 is up-regulated in kidneys in NTS and that Tim3 exerts protective roles in the course of disease.
Find related publications in this database (using NLM MeSH Indexing)
Acute-Phase Proteins - urine
Albumins - chemistry
Animals -
Creatinine - urine
Humans -
Kidney - metabolism Kidney - pathology
Kidney Diseases - metabolism
Lipocalins - blood Lipocalins - urine
Lymph Nodes - pathology
Male -
Membrane Proteins - biosynthesis Membrane Proteins - physiology
Mice -
Mice, Inbred BALB C -
Mice, Inbred C57BL -
Nephritis - blood Nephritis - pathology
Oncogene Proteins - blood Oncogene Proteins - urine
Proto-Oncogene Proteins - blood Proto-Oncogene Proteins - urine
Receptors, Virus - biosynthesis Receptors, Virus - physiology
Th1 Cells - cytology

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