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Comparison of conventional and microwave‐assisted processing of mouse retinas for transmission electron microscopy
Author(s) -
Wendt K. D.,
Jensen C. A.,
Tindall R.,
Katz M. L.
Publication year - 2004
Publication title -
journal of microscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.569
H-Index - 111
eISSN - 1365-2818
pISSN - 0022-2720
DOI - 10.1111/j.0022-2720.2004.01310.x
Subject(s) - ultrastructure , retina , fixation (population genetics) , transmission electron microscopy , photoreceptor cell , microwave , retinal , electron microscope , materials science , biophysics , anatomy , biology , optics , nanotechnology , physics , neuroscience , botany , biochemistry , quantum mechanics , gene
Summary Conventional fixation and processing of mammalian retinal tissues for transmission electron microscopic (TEM) examination is slow and produces ultrastructural artefacts in the photoreceptor cell layer. Among these artefacts are gaps between photoreceptor outer segment disc membranes and between photoreceptor cells in the region of the retina where the cell nuclei are located. A study was undertaken to determine whether a much more rapid microwave‐assisted fixation and processing protocol would have an effect on the quality of ultrastructural preservation of the retina, particularly on the photoreceptor cell artefacts. The overall ultrastructural preservation of the retina was similar for the conventional and microwave‐assisted techniques. However, the magnitudes of the photoreceptor artefacts were significantly reduced when microwave irradiation was used during primary fixation and processing. It is clear that, at least for the retina, employing microwave irradiation during specimen preparation for TEM results in superior ultrastructural preservation with a substantial reduction in the time required for sample preparation.