Summary -The ultrastructural localization of glucose-6-phosphatase activity and glycogen were investigated in the longissimus dorsi and biceps femoris muscles of normal and splaylegged newborn piglets. Significant differences were ascertained in the distribution of the reaction product of glucose-6-phosphatase activity between the two groups of animals. A fine precipitate was found in the sarcoplasmic reticulum and in the perinuclear cisternae of normal piglet muscles. In splaylegged muscles, variable deposits of coarse reaction product were observed within the extremely dilated cistemae of sarcoplasmic reticulum at their periphery. Moreover, both longitudinal and transversal ultrathin sections of these muscles showed a reduced number of myofibrils and an increased accumulation of glycogen (especially within the large extramyofibrillar spaces) in comparison with muscles of normal piglets. splayleg / muscle ultrastructure / glucose-6-phosphatase / glycogen / pig Résumé ― Démonstration ultrastructurale de l'activité glucose-6-phosphatase et du glycogène dans les muscles squelettiques de porcelets nouveau-nés atteints du syndrome d'abduction des membres. La localisation ultrastructurale de l'activité glucose-6-phosphatase et du glycogène a été analysée dans des muscles (longissimus dorsi et biceps femoris) de porcelets nouveau-nés normaux ou atteints du syndrome. Des différences significatives ont été mises en évidence dans la distribution du produit de réaction de la glucose-6-phosphatase entre les deux groupes d animaux. Un fin précipité a été observé dans le réticulum sarcoplasmique et l'espace périnucléaire dans les muscles de porcelet témoin. Dans les muscles anormaux, des dépôts variables et grossiers du produit de réaction ont été localisés dans les vésicules très dilatées du réticulum sarcoplasmique. De

Ultrastructural changes of the germinal vesicle during the growth of rabbit oocytes were studied by means of light and electron microscopy, 3H-uridine autoradiography, Ag-NOR staining and E-PTA staining. Particular interest was paid to the nucleologenesis and condensation of chromatin. In contrast to other mammalian species, chromosome condensation in rabbit oocytes occurred concomitantly with rRNA synthesis-dependent nucleolar compaction and preceded nuclear envelope breakdown and resumption of meiosis.

Argyrophilic nuclear proteins, known to be functionally associated with ribosomal genes, were localized, in four-, eight-, and 16-cell bovine embryo blastomere nuclei using two different silver-staining procedures. Within the eight-cell cleavage stage by the process of embryonal nucleologenesis in the cow embryo the full-capacity ribosome-producing machinery is established. In the four-cell embryo, many patches and islands of argyrophilic (Ag+) material were detected in the nucleoplasm. The nucleolus-precursor bodies (NPBs), composed uniformly of a homogeneous compact mass, were completely devoid of any silver staining. On the other hand, clear-cut localization of argyrophilic proteins was detected during the eight-cell stage either inside the transforming NPBs or in the close vicinity, or in the already differentiated nucleolus. In compact, nonvacuolated NPB, an intensive Ag+ area was detected, in the form of a lenticle, at the periphery of the NPB. During and following vacuolation of the NPB, no Ag+ was detected inside these vacuoles. It was seen, however, in the dense fibrillar nucleolar component surrounding the smaller vacuoles formed at the time of the establishment of nucleolar structure. Ag+ areas were seen repeatedly in the vicinity of NPBs, probably a part of the nucleolus-associated chromatin or, alternatively, representing the extranucleolar bodies. In blastomere nuclei of 16-cell embryos, already possessing reticulated nucleoli known from intensively synthesizing somatic cells, the silver-staining pattern corresponded to the usual situation in differentiated cells: slight staining of fibrillar centers, heavy labelling in the dense fibrillar component, and absence of silver deposits in the granular component.(ABSTRACT TRUNCATED AT 250 WORDS)

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Summary ― The presence of acidic argyrophilic protein(s) in cumulus cells and oocytes was examined in bovine, ovine, porcine and murine cumulus-oocyte complexes (COCs) using a specific silverstaining method. The COCs were isolated from small (1 mm) or large (3-5 mm) antral follicles; they were fixed immediately after slaughter (first group) or after transfer to the laboratory (ca 60 min, second group) and then silver stained according to Likovsky'and Smetana