[An analysis of the supramolecular organization of the olfactory neuroepithelium in the rat by freeze etching with rotary platinum-carbon shadow-casting].

The rat olfactory epithelium was analysed by freeze-deep etching and Pt/C rotary replication. Ultrathin sections and freeze-etching findings of proximal (dendrite) and distal (axon) parts of bipolar olfactory neurons are examined. The supramolecular organization of neuron membranes and intracellular cytoskeleton structure is studied.

[The use of cryomethods for research on the sarcomere ultrastructure of rabbit skeletal muscles].

The ultrastructure of sarcomeres of glycerinated rabbit psoas muscle was studied using freeze-fracture-etching, freeze-drying and optical diffraction techniques in comparison with the investigation of this muscle by plastic sections and negative staining methods. In frozen and dried myofibrils isolated from the above muscle the stripes of minor proteins location in A- and I-disks were clearly seen. The pivot structure in thick filaments was revealed in longitudinal fractures of the muscle.

[Ultrastructural analysis of the action of centrophenoxine on retrovirus-transformed cells].

The ultrastructure of hybridoma cells cultured with 5.10(-4) centrophenoxine (CP) has been studied. It is shown that CP effects hybridomas and prevents retrovirus exocytosis.

Ultracytochemical localization and microprobe quantitation of calcium stores in the insect oocyte.

Detection of calcium in the follicles of Galleria mellonella (Lepidoptera) was performed using two cytochemical methods. Calcium precipitation was obtained either with ammonium oxalate (AO) or with N,N-naphtaloylhydroxylamine (NHA). In both cases the X-ray "on line" analysis monitored the presence of calcium in the oocytes, which was correlated with the accumulation of yolk spheres.

[Local x-ray spectral microanalysis in cell biology. The study of sections of hydrated biological tissues].

Rules required for fixation of tissues are considered aimed for a further localization of chemical elements in these tissue by means of local X-ray microanalysis. In addition, difficulties involved in fixation of diffusible elements, such as potassium or sodium, are mentioned. Physical bases of preparation of hydrated tissues for X-ray analysis are discussed.