Cell Membrane Nanostructure is Altered by Heat-Induced Antigen Retrieval: A Possible Consequence for Immunocytochemical Detection of Membranous Antigens

• Published in: Microscopy and microanalysis Vol. 26; no. 1; pp. 139 - 147
• Main Authors: Cizkova, Katerina, Malohlava, Jakub, Tauber, Zdenek
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.02.2020
• Subjects: Acetone; Alcohol; Antibodies; Antigens; Atomic force microscopy; CD44 antigen; CD9 antigen; Cell adhesion & migration; Cell membranes; Cell surface; Correlation coefficients; E-cadherin; Epidermal growth factor; Epidermal growth factor receptors; Geologic depressions; Growth factors; Heat; Hydrogen bonds; Immunoglobulins; Microscopy; Paraffin; Paraffins; Proteins; Retrieval; Skewness; Staining; Surface antigens; Topography; United States > US; immunostaining; membrane antigens; atomic force microscopy; cell surface nanostructure
• ISSN: 1431-9276; 1435-8115
• DOI: 10.1017/S1431927619015113

Heat-induced antigen retrieval (HIAR) treatment improves the antigen immunodetection in formalin-fixed, paraffin-embedded tissue samples and it can also improve the detection of intracellular antigens in alcohol-fixed cytological samples, although it could deleteriously impact immunodetection, particularly that of membranous antigens. We examined the differences in cell surface topography on MCF7 cells fixed in methanol/acetone (M/A) or 4% paraformaldehyde (4% PFA), as well as the changes caused by HIAR treatment at three different temperatures (60, 90, and 120°C), using atomic force microscopy. Furthermore, the consequences for immunostaining of five membranous antigens [epidermal growth factor receptor (EGFR), E-cadherin, CD9, CD24, and CD44] were examined. Our results illustrate that while there was no one single optimal immunostaining condition for the tested antibodies, the surface topography could be an important factor in successful staining. Generally, the best conditions for successful immunostaining were M/A fixation with no HIAR treatment, whereas in 4% PFA-fixed cells, HIAR treatment at 120°C was optimal. These conditions showed similarity in cell surface skewness. A correlation factor between successful immunocytochemical staining and the skewness parameter was 0.8000. Our results indicate that the presence of valleys, depressions, scratches, and pits on the cell surface is unfavorable for the successful immunodetection of cell surface antigens.