Open AccessStudy of SEM preparation artefacts with correlative microscopy: Cell shrinkage of adherent cells by HMDS‐drying
Author(s) -
KatsenGloba Alisa,
Puetz Norbert,
Gepp Michael M.,
Neubauer Julia C.,
Zimmermann Heiko
Publication year - 2016
Publication title -
scanning
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.359
H-Index - 47
eISSN - 1932-8745
pISSN - 0161-0457
DOI - 10.1002/sca.21310
Subject(s) - shrinkage , scanning electron microscope , materials science , microscopy , biomedical engineering , composite material , chemistry , pathology , medicine
Summary One of the often reported artefacts during cell preparation to scanning electron microscopy (SEM) is the shrinkage of cellular objects, that mostly occurs at a certain time‐dependent stage of cell drying. Various methods of drying for SEM, such as critical point drying, freeze–drying, as well as hexamethyldisilazane (HMDS)‐drying, were usually used. The latter becomes popular since it is a low cost and fast method. However, the correlation of drying duration and real shrinkage of objects was not investigated yet. In this paper, cell shrinkage at each stage of preparation for SEM was studied. We introduce a shrinkage coefficient using correlative light microscopy (LM) and SEM of the same human mesenchymal stem cells (hMSCs). The influence of HMDS‐drying duration on the cell shrinkage is shown: the longer drying duration, the more shrinkage is observed. Furthermore, it was demonstrated that cell shrinkage is inversely proportional to cultivation time: the longer cultivation time, the more cell spreading area and the less cell shrinkage. Our results can be applicable for an exact SEM quantification of cell size and determination of cell spreading area in engineering of artificial cellular environments using biomaterials. SCANNING 38:625–633, 2016. © 2016 Wiley Periodicals, Inc.