The influence of the embedding medium is of critical importance in the observation of nucleoprotein structures in thin sections. The use of conventional epoxi media requires dehydratation, impregnation and subsequent polymerization, which may produce drastic alterations in the fine structure of chromatin. The use of water soluble embedding media may lead to improvements in the preservation of ultrastructure. In this paper we explore the differences which may be detected in nucleohistone fibers embedded in different media.Spermatozoa from Holothuria polii were subjected to moderate lysis in either 0.15M NaCl, ImM Tris-HCl, 0.4mM CaCl2, pH 8.0 (a) or 0.25M sucrose, 0.4mM CaCl2 (b) and then fixed by addition of 2 % glutaralde- hyde. Embedding was carried out as described in the literature in the following media: araldite-epon mixture (AREPO), glycol methacrylate (GMA, 1), hydroxipropyl methacrylate (HPMA, 2) and bovine serum albumin (BSA, 3) or histones.
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