Document Detail


Problems in preparation of chromosomes for scanning electron microscopy to reveal morphology and to permit immunocytochemistry of sensitive antigens.
MedLine Citation:
PMID:  9601537     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Although much information about chromosome structure and behaviour has been obtained using light microscopy, greater resolution is needed for a thorough understanding of chromosome organisation. Scanning electron microscopy (SEM) can provide valuable data about these three-dimensional organelles. The introduction of methods using osmium impregnation of methanol-acetic acid-fixed chromosome spreads revolutionised matters, producing life-like images of chromosomes. Nevertheless, it became clear that osmium impregnation introduced various artefacts, although the resulting images were still useful. Methanol-acetic acid-fixed chromosomes are, in fact, flattened on the glass substratum, and the 3-dimensional appearance obtained after osmium impregnation is the result of swelling during this process. At the same time, the fibrous substructure of the chromosomes becomes much coarser. More recently a number of alternative methods have become available for studying chromosomes by SEM. Isolated chromosomes, that have not been allowed to dry during preparation, retain a 3-dimensional appearance without osmium impregnation, and the same is true of methanol-acetic acid-fixed chromosomes that have been treated with 45% acetic acid and processed without drying; however, these methods do not permit the routine production of intact metaphase spreads. Use of cytocentrifuge preparations obviates the use of acetic acid fixation and osmium impregnation, produces intact metaphase spreads, and permits the immunocytochemical detection of antigens that are easily destroyed by routine fixation procedures.
Authors:
A T Sumner
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Scanning microscopy. Supplement     Volume:  10     ISSN:  0892-953X     ISO Abbreviation:  Scanning Microsc. Suppl.     Publication Date:  1996  
Date Detail:
Created Date:  1998-06-18     Completed Date:  1998-06-18     Revised Date:  2007-08-02    
Medline Journal Info:
Nlm Unique ID:  8710881     Medline TA:  Scanning Microsc Suppl     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  165-74; discussion 174-6     Citation Subset:  IM    
Affiliation:
MRC Human Genetics Unit, Western General Hospital, Edinburgh, U.K.
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MeSH Terms
Descriptor/Qualifier:
Acetic Acid
Animals
Antigens / analysis*
CHO Cells
Centrifugation / methods
Chromosomes / chemistry,  immunology,  ultrastructure*
Chromosomes, Human / chemistry,  immunology,  ultrastructure*
Cricetinae
Histocytological Preparation Techniques
Humans
Immunohistochemistry
Metaphase / physiology
Microscopy, Electron, Scanning / methods*
Osmium
Tissue Fixation
Chemical
Reg. No./Substance:
0/Antigens; 64-19-7/Acetic Acid; 7440-04-2/Osmium

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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