NUCLEAR ORGANIZER REGIONS (AGNORS) STAINING ON UNDECALCIFIED BONE EMBEDDED IN RESIN - LIGHT AND TEM METHODOLOGIES

Citation
D. Chappard et al., NUCLEAR ORGANIZER REGIONS (AGNORS) STAINING ON UNDECALCIFIED BONE EMBEDDED IN RESIN - LIGHT AND TEM METHODOLOGIES, Journal of histotechnology, 19(1), 1996, pp. 27-32
Citations number
34
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
01478885
Volume
19
Issue
1
Year of publication
1996
Pages
27 - 32
Database
ISI
SICI code
0147-8885(1996)19:1<27:NOR(SO>2.0.ZU;2-D
Abstract
Nuclear organizer Region (NORs) are parts of the nucleoli involved in the synthesis of ribosomes. Silver-stainable proteins of the nucleolar organizer regions (AgNORs) which are increased in neoplastic cells, c an be localized in tissues embedded in resins. The method was adapted to bone, which needs to be processed undecalcified for histomorphometr ic purposes. Sections of undecalcified biopsies embedded in methacryli c resins were extensively demineralized in EDTA. They were stained for AgNORs and conterstained with metanil yellow. Sections were flattened with polyvinyl alcohol (a hydrophilic glue), which makes them suitabl e for light microscopy. The same method was applied for transmission e lectron microscopy (TEM) by embedding undecalcified blocks in an hydro philic resin (LR-White). Ultrathin sections of bone mounted on gold gr ids could be stained for AgNORs after EDTA demineralization. The inter est of hpdrophilic resins as embedding media was evidenced for AgNORs staining.