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A novel evaluation method for paraffinized human renal biopsies using quantitative analysis of microdissected glomeruli and VCAM-1 as marker of inflammatory mesangial cell activation
Author(s) -
Jochen W.U. Fries,
Tanja Roth,
HansPeter Dienes,
Manfred Weber,
Margarete Odenthal
Publication year - 2003
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfg045
Subject(s) - mesangial cell , lupus nephritis , nephropathy , pathology , mesangium , medicine , vcam 1 , cell adhesion molecule , housekeeping gene , nephritis , mesangial proliferative glomerulonephritis , glomerulonephritis , reverse transcription polymerase chain reaction , gene expression , microbiology and biotechnology , immunology , biopsy , renal biopsy , kidney , biology , gene , endocrinology , icam 1 , disease , biochemistry , diabetes mellitus
In the glomerular mesangium, immunologic and/or infectious activation of the inflammatory, NF-kappaB-mediated signal pathway can induce a progression of already existing mesangial lesions in non-immunologic and immunologic glomerular disease. This progression is preceded by upregulated mesangial gene expression of which the vascular cell adhesion molecule-1, VCAM-1 (vascular cell adhesion molecule-1), is a well-established marker. Its evaluation on minimal tissue such as routinely paraffinized needle core biopsies is not established and needs the development of a novel evaluation method more meaningful than common immunohistology.

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