Literature DB >> 12658346

Immunohistochemical diagnosis of Alport's syndrome in paraffin-embedded renal sections: antigen retrieval with autoclave heating.

Ichiro Naito1, Yoshifumi Ninomiya, Shinsuke Nomura.   

Abstract

Alport's syndrome (AS) is a hereditary renal disease caused by mutations in the genes encoding collagen type IV. Immunohistochemical analysis of the alpha chains of collagen type IV has been found to be useful for the diagnosis of this disease. The monoclonal antibodies (mAbs) generated by us recognize alpha 1(IV) through alpha 6(IV) chains of collagen type IV on fresh-frozen sections but not on paraffin-embedded sections. Antigen retrieval by autoclave heating has been found to restore the epitopes recognized by the mAbs; however the heating conditions had not been well established. In this study, the heating conditions were carefully examined using renal sections obtained from AS and non-AS patients. The heating was performed in an autoclave, at 105 degrees -127 degrees C for 6-8 min. During the heating, the sections were immersed in 0.2 N HCl solution (pH 0.9). Then, the mAbs were applied for 30 min, and the bound mAbs were detected using the LSAB kit. The optimal temperature for the antigen retrieval varied among specimens, and was dependent on the type of basement membrane examined. Thus, it was considered that heating at two or three different temperatures could be helpful for the precise diagnosis of AS. Adopting the antigen retrieval method could extend the possibility of immunohistochemical diagnosis of AS to cases without using fresh-frozen sections.

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Year:  2003        PMID: 12658346     DOI: 10.1007/s007950300000

Source DB:  PubMed          Journal:  Med Electron Microsc        ISSN: 0918-4287


  3 in total

1.  Antigen retrieval with protease digestion applied in immunohistochemical diagnosis of Alport syndrome.

Authors:  Na Guan; Li-Xia Yu; Guo-Hong Wu; Yan Xing; Jie Ding
Journal:  Nephrol Dial Transplant       Date:  2008-06-03       Impact factor: 5.992

2.  Siblings with Alport's syndrome showing unique staining patterns for alpha5(IV) and alpha6(IV) chains of collagen type IV.

Authors:  Takayuki Tsuji; Yoshihide Fujigaki; Masanori Sakakima; Yoshikazu Sado; Akira Hishida
Journal:  Clin Exp Nephrol       Date:  2010-03-09       Impact factor: 2.801

3.  COL4A6 is dispensable for autosomal recessive Alport syndrome.

Authors:  Tomohiro Murata; Kan Katayama; Toshitaka Oohashi; Timo Jahnukainen; Tomoko Yonezawa; Yoshikazu Sado; Eiji Ishikawa; Shinsuke Nomura; Karl Tryggvason; Masaaki Ito
Journal:  Sci Rep       Date:  2016-07-05       Impact factor: 4.379

  3 in total

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