Archives d'anatomie microscopique et de morphologie experimentale最新文献

The ontogenesis of the corpus callosum is inextricably linked with the various processes controlling prosencephalic development. Our study is based on series of frontal and sagittal sections through the prosencephalon of 16 and 17 day mouse embryos and on ultrathin sections of the septum, particularly of the zone where the callosal fibres cross. The septum, which contains the first callosal fibres, does not undergo the fusional process described by other authors. The passage of pioneer fibres from one hemisphere to the other is preceded by the degeneration and death of the atrocytes of the cortical plate in the fundus of the interhemispheric issure, and by proliferation of the subependymal cells. The proliferation and migration of the subependymal cells from the medial angles of the lateral ventricles may well assist the passage of pioneering callosal fibres.

The distribution of fibronectin (FN) in the dental pulp and gingiva of the human adult was investigated by indirect immunofluorescence and indirect immunoperoxidase techniques. FN could not be demonstrated in the connective tissue of the dental pulp even in the blood vessels. On the contrary, a positive stain was obtained in the ground substance at the base of the odontoblast cell bodies and in various structures of a denticle which was accidentally found in the pulp of one of the examined teeth. The lack of FN in the dental pulp could mean that this tissue, sometimes considered to be of an immature and undifferentiated type, is instead a mature one. The subepithelial connective tissue and the epithelium of the gingiva were examined. The distribution of FN in the connective tissue of the gingiva was found to be similar to that described in other types of connective tissue; high concentrations were found both in the epithelial cells and around them. This finding is described here for the first time and remains to be verified in other types of stratified epithelia.

Freeze-fracture was used to study Anura Amphibia primordial germ cells (PGCs) from the time when they have invaded genital ridges until the time when sexual differentiation has begun. We observed tight junctions with a variety of configurations including linear, macular, and extensive occluding cross-linking complexes. True gap junctions were not observed. Rod-shaped particles were found disseminated among particles on the P fracture faces of the germ cells.

Pieces of trypsin-isolated 14-day embryonic mouse epidermis were recombined with various living or non-living dermal or non-dermal substrates, in order to analyse the reconstruction of the dermal-epidermal junction. The constitution and ultrastructure of the epidermal basement membrane were characterized by immunolabelling of laminin, type IV collagen and bullous pemphigoid antigen, and by transmission electron microscopy. Trypsin treatment of dorsal skin followed by dermal-epidermal separation does not visibly damage the epidermal basement membrane, which remains attached to the lower face of epidermis. When freshly isolated epidermis is reassociated with dermis, the basement membrane is first degraded during the first 4 h of culture, then reconstituted within 24 h. When epidermis is cultured in isolation the basement membrane disappears within 4 h and is not reconstructed. Epidermis, precultured for 4 h and thus deprived of its basement membrane prior to reassociation, is able to reconstruct an antigenically and ultrastructurally normal basement membrane, when recombined with living or frozen-killed (-20 degrees C) dermis, with muscle tissue, or with a film of fibrous type I collagen. No basement membrane is reconstituted when the epidermis is recombined with heat (100 degrees C) killed dermis. It is concluded that, in the reconstituted epidermal basement membrane, laminin, type IV collagen, bullous pemphigoid antigen, and lamina densa are of exclusive epidermal origin.

12 1/2-15 1/2 day embryonic mouse testes of 129/terSv and CBA/T6T6 strains were transplanted under the kidney capsule of adult hosts. After 3-5 days in 41% of CBA/T6T6 transplants and in 82% of 129/terSv transplants a limit number of germ cells began meiosis. The percentage of meiotic germ cells was inversely related to the total number of gonocytes and the organization of seminiferous cords. The presented evidence indicates that the ability of the germ cells to begin meiosis precociously depends on: 1) genotype of donor embryos; 2) age of transplanted testis, and 3) using whole of half of gonad for transplantation. After 10-15 days in two out of 46 129/terSv testes (4%) growing oocytes were observed.

The influence of the fixation procedure on the localization of albumin and transferrin in adult rat liver has been carried out using an indirect immunoperoxidase technique at the light and electron microscopic levels. Perfusion and immersion fixations with different concentrations of paraformaldehyde (with or without addition of glutaraldehyde) have been investigated. According to the mode of fixation (perfusion versus immersion) and the concentration of the fixative, the number of albumin and transferrin containing hepatocytes could vary from 10% to 100%, and different labeling patterns could be observed at the electron microscopic level. For the same concentration of fixative, a perfusion fixation induces a less intense labeling than an immersion fixation. Thus similar results are obtained after immersion fixation in 6% paraformaldehyde + 0.25% glutaraldehyde or after perfusion fixation in 4% paraformaldehyde + 0.025% glutaraldehyde. Similar data are noticed after immersion fixation in 4% paraformaldehyde or after perfusion fixation in 1% paraformaldehyde + 0.025% glutaraldehyde. Moreover, perfusion fixation induced a more fine cell structure preservation than immersion fixations and avoided the appearance of zones of fixation.

The endometrium of rabbits, treated by the usual pharmacology methods designed for the measurement of the pseudogestagen effect, was studied by scanning electron microscopy. Estrogen stimulation was followed by a multiplication of the number of ciliated cells. Treatment with progesterone lead to a decrease in the numbers of microvilli and to the appearance of rounded bulges which increased in numbers as the progesterone dose level increased. These changes were quite close to those observed in post menopausal women under estro-progestogen treatment.

The influence of an initial stress attack (a subcutaneous saline injection plus rough handling) on the morphofunctional behaviour of the pineal gland was studied. Both light and electron microscopy pointed to an enhanced endocrine activity on the gland parenchyma. The occurrence of the clusters of highly activated light pinealocytes, as well as the appearance of two functionally different types of these cells, revealed that the introduction of the pineal gland to a new stress-induced steady state was based on the gradual promotion of a number of pinealocytes to the level of a high activity. Dark pinealocytes were less numerous and rather engaged in the synthesis than in the secretion. The ultrastructural characteristics of both pinealocyte populations show that the pineal gland meets the secretory demands upon an initial stress attack by a striking discharge of its active compounds and a successive activation of a new elaborative cycle. The morphodynamic conclusion about an enhanced pineal gland secretory activity is fully evaluated in the change of the rate of prolactin surge. A possible impact of the morphodynamic reactivity of the endocrine parenchyma of the pineal gland upon the functional interpretation of the morphological properties of pinealocytes in case of some manipulative procedures with animals was discussed.

A cell proliferation study during wound healing of the excised integument of the flank in 5-day chick embryos was performed by pulse labelling using a single isotope (tritiated thymidine). The embryos were operated according to the experimental protocol already published (Thevenet and Sengel, 1973; Thevenet, 1981). 20 microCi of 3H-thymidine were deposited on the integument of the right flank of unoperated (controls) and operated embryos fixed 1 (start control), 2, 12 and 24 h after the excision. Mean labelling index of the unoperated epidermis was 13.7% at 5 days and 21.5% at 6 days of incubation. 2 hours after the excision, labelling index of the operated epidermis increased, on average, to 175% with respect to the labelling index of the controls, in the proximal zones near the wound edges; in the distal zones, the labelling index was lower than that of the controls. The labelling index in the dermis was, on average, 23.4% at 5 days and 28.5% at 6 days of incubation. 2 hours after the excision, the labelling index of the operated dermis increased, on average, to 165% with respect to that of the controls; later it decreased again and remained slightly higher or slightly lower than that of the controls. The increase of the labelling index of the operated integument persisted for a maximum of 6 h after the excision.