The use of MAB 1977 monoclonal antibody for the immunohistochemical localization of beta 1 integrins in paraffin-embedded human kidney

被引:2
|
作者
Bernardini, N [1 ]
Bianchi, F [1 ]
Lupetti, M [1 ]
Dolfi, A [1 ]
机构
[1] UNIV PISA,FAC MED & CHIRURG,IST ANAT UMANA NORMALE,CATTEDRA ISTOL & EMBRIOL,I-56126 PISA,ITALY
关键词
beta; 1; integrin; paraffin-embedding; immunoperoxidase; kidney;
D O I
10.1177/030089169708300310
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims and background: Integrins are widely known cell membrane receptors for extracellular matrix molecules. The beta 1 integrin subgroup is mainly expressed by kidney cells; immunolocalization of these molecules is usually carried out on cryostatic sections. A commercial monoclonal antibody directed against the human beta 1 integrin was tested in order to design a method for the detection of this antigen in formalin-fixed, paraffin-embedded human kidney tissue. Methods: Specimens obtained from nephrectomies were fixed with 10% formalin and embedded in paraffin. Three different detection protocols were applied after incubation with the antihuman beta 1 integrin monoclonal antibody (MAB 1977): 1) immunoperoxidase with labelled streptavidin biotin (LSAB), using biotinylated secondary antibodies, peroxidase-labeled biotin-streptavidin, and 3,3'-diaminobenzidine tetra-hydrochloride (DAB) as the revealing system; 2) immunoperoxidase with tyramide signal amplification (TSA), using biotinylated secondary antibodies, streptavidin-peroxidase, tyramide, streptavidin-peroxidase again and DAB; 3) indirect immunofluorescence with fluorescein-labeled anti-mouse immunoglobulins. Results: The best results were obtained with the LSAB detection protocol preceded by a predetection step with proteinase k. Proteinase k pretreatment did not significantly damage the tissue morphology and successfully unmasked beta 1 integrin antigens. Nonspecific background staining was reduced by a blocking step with swine serum. Similar results were obtained with the TSA detection method; however, although lower concentrations of anti-beta 1. integrin immunoglobulins and of secondary biotinylated antibody were employed, there was more undesired background staining than with the LSAB protocol. Conclusions: The method reported and discussed here may represent a valid tool for research and diagnostic applications based upon detection of beta 1 integrin in paraffin-embedded human tissues.
引用
收藏
页码:673 / 678
页数:6
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