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Um die Abhängigkeit der erythropoietischen Zellformen von ihrer Stellung im Generationszyklus (G1, S und G2) zu untersuchen, wurde das Knochenmark von vier Normalpersonen mit der Kombination von zytophotometrischer DNS-Bestimmung (Feulgen-Photometrie) und autoradiographischer Technik mit 3H-TdR (in vitro) untersucht. Die Zellen wurden vor dieser Untersuchung in den nach Pappenheim gefärbten Ausstrichen differenziert. Sowohl in der Gruppe der basophilen Erythroblasten (E1-E3) als auch bei den polychromatischen Normoblasten (E4) wurde eine postmitotische (G1) und eine prämitotische Ruhephase (G2) nachgewiesen. Beide Zellgruppen waren zu ca. 65% mit3H-TdR markiert (S). Unter den basophilen Erythroblasten war bei E1 eine G2-Phase, jedoch keine G1-Phase nachweisbar. Demgegenüber fand sich bei E3 eine ausgeprägte G1-Phase, hingegen keine G2-Phase. Bei E2 war sowohl eine G1-Phase als auch eine G2-Phase erkennbar. Nach diesen Befunden stellen die Erythroblasten E1-E3 keine Zellgruppen mit jeweils vollständigem Generationszyklus dar, sondern sind als ein Zellkompartment zu verstehen, in dem die G1-Phase vorwiegend durch die kleineren Zellen, die zytologisch die Merkmale der basophilen Normoblasten besitzen, und die G2-Phase vorwiegend durch die größeren Zellen vom Typ der Proerythroblasten und Makroblasten repräsentiert wird.

The ultrastructure of the intermediate lobe of the hypophysis was studied in Anolis carolinensis with the use of a threefold aldehyde fixative. Lizards with a brown skin were selected. The possibility of two types of secretory cells is discussed; neither cell type is innervated. Type I cells are rarely found and contain dense granules approximately 0.3 μm in diameter; Type II cells vary widely in secretory activity. Most of the Type II cells contain a large number of dense secretory granules (up to about 1.3 μm in diameter) almost filling the cytoplasm. Rough endoplasmic reticulum (RER), Golgi apparatus and mitochondria are poorly developed. Only some of these cells show signs suggesting a high secretory activity, namely a well developed RER, Golgi apparatus and numerous mitochondria. In these cells the RER sometimes forms large intracisternal droplets (up to 7 μm in diameter). Two of the animals exhibited a more uniform, high secretory activity. Large (about 2 μm in diameter), pale vacuoles, probably of extracellular character, were found mostly in the vicinity of the perivascular septum. Their role in the release of MSH is discussed. The present data, which are discussed with reference to earlier findings (Forbes, 1972), form the morphological basis for an experimental study on regulation of MSH release (Larsson et al., 1979).

Electron-microscopic studies of the neural complex (neural gland, dorsal strand, and cerebral ganglion) of an ascidian, Halocynthia roretzi, were performed, paying particular attention to the secretory systems. We found that cells scattered along the dorsal strand and neural cells in the cerebral ganglion contained electron-dense secretory granules of variable size. Immunoelectron-microscopic studies with an antiserum to bullfrog prolactin revealed that the secretory granules (100–250 nm in diameter) of some granulated cells contained a prolactin-like substance. Cells belonging to the neural gland and dorsal strand neither contained electron-dense granules nor showed immunoreactivity. The possibility that cells in the cerebral ganglion and those along the dorsal strand are phylogenetic progenitors of vertebrate adenohypophyseal cells is discussed.

By means of light-microscopic immunohistochemistry the perikarya of the luliberin-(LRF-) and somatostatin systems of neonate rats were found to be in differing stages of development. At a time point when the LRF-producing neurons had obviously attained their final shape and size, the somatostatin-immunoreactive perikarya were still in a postnatal phase of maturation. Whereas the number of the latter perikarya increases with advancing age, the number of LRF-immunoreactive perikarya decreases significantly from postnatal day 7 onward. Both peptide-hormone systems do not project concomitantly and to the same extent to their principal neurohemal regions in the organum vasculosum laminae terminalis (OVLT) and the median eminence (ME). In all presently studied stages of development, despite considerable individual variations in one age group, among the components of the LRFsystem the OVLT displays a more intense immunoreactivity than the ME. The somatostatin system, however, projects to the OVLT with a conspicuous temporal delay compared to the ME, and, furthermore, in the OVLT the pattern of immunoreactivity characteristic of adult rats is not yet attained at postnatal day 21. Evidence for differences in the immunoreactivity between male and female animals was restricted to the LRF-system. Finally, the results obtained on the stria terminalis speak in favour of the fact that the long-range extrahypothalamic projections of the somatostatin system also undergo postnatal maturation. In the stria terminalis, somatostatin-immunoreactive fibers can be demonstrated initially on postnatal day 7. They attain their full immunoreactivity on postnatal day 21. Furthermore, in the bed nucleus of the stria terminalis an intermittent cytoplasmic immunoreactivity is observed, which is limited to the animals of postnatal day 7 and disappears completely during the further course of development.

Migration of bilayered epidermal cell sheets out of explants of tadpole tails (Xenopus laevis) were investigated with time-lapse cinemicrography using reflection-contrast optics. Cell-sheet formation begins beneath the explant in a region where it is closely attached to the coverslip. A single basal cell extends a lamellipodium through the outer (surface) epidermal layer and starts moving in a direction free of attached cells. This cell remains connected to the following basal cell, which the also extends a lamellipodium onto the glass. The cell sheet develops as increasingly more adjacent basal cells start to migrate. Surface cells do not actively locomote but they remain attached to the basal cells and to adjacent surface cells. Thus, they are transported as an intact cell layer, and consequently the in situ arrangement of the tadpole epidermis is largely preserved in the cell sheet, i.e., basal cells adhere to the substratum and are covered by outer cells (surface cells) which face the culture medium. Basal cells extend lamellae beneath the rear end of the preceding cell, which is slightly fifted off the substratum. The direction of locomotion is determined by the frontal cells. Cell-sheet enlargement and locomotion cease when all the epidermal cells facing the coverslip have left the explant, and the cell sheet and epidermis covering the explant form a continuous layer.

The bridge-partitioning complex present in pre-existing intercellular bridges of dividing spermatogonia in the juvenile golden hamster testis was studied by electron microscopy. There is a close temporal adjustment in the appearance of this structure to those stages of mitosis during which the cells are without a nuclear membrane, i.e., the bridge-partitioning complex is formed at the transition between prophase and prometaphase and gradually disappears during telophase. In addition, in a certain form of degenerative dividing germ cells, which completely lack a bridge-partitioning complex in pre-existing intercellular bridges, condensed chromatin not surrounded by a nuclear membrane occasionally projects through these open bridges and thus may well change over to a neighboring cell of the same clone. These results strongly indicate an essential barrier function of the bridge-partitioning complex. It temporarily prevents intraclonal exchange of nuclear material during those stages of mitosis where a nuclear membrane is lacking and, thus, maintains genetic integrity of male germ cells during synchronous divisions.

By back-filling the nervus corporis allati II (NCA2) with Co2+ and precipitating the sulfide, two groups of somata (A and B) are revealed on the ipsilateral side of the subesophageal ganglion (SG). These occur ante-roventrally, adjacent to the midsaggital plane. Group A consists of two cells; group B of five. Their processes form two discrete tracts issuing dorsoposteriorly into the neuropile between and slightly behind the circumesophageal connectives (CEC). After producing separate arborization fields in the dorsal neuropile, the tracts circumscribe the base of the ipsilateral CEC, unite, and their seven fibers enter NCA2 anteriorly. Prograde diffusion reveals 4-6 NCA2 axons penetrating the corpus allatum (CA) near a cap-like neurohemal organ. These axons form the transverse allatal tract (TAT), from whence they branch amongst the CA cells, and into the “cap”, the postallatal nerves, and the opposite CA. Electron microscopy of transverse sections demonstrates nine neurosecretory axons entering the SG through NCA2. Proximal to the CA, NCA2 consists of a central bundle of neurosecretory axons and a peripheral zone confluent with the CA “cap”. Depending upon the level of sectioning, there are 7–20 axons at the center, and seven pass into the TAT. The peripheral zone has the structure of a neurohemal organ.

Time-lapse cinematography elucidates the genesis of a uniform and approximately linearly arranged myogenic cell aggregate, stemming from two larger cell groups. The ultimate aggregate is created by continuous movement of one cell group toward the other. Following this motion, the angle between the cell groups is reduced as they approach each other. Different patterns of cell motility can be recognized. Some cells move in a preferred direction in relation to the aggregate as a whole, whereas others alter their direction of movement. The myogenic cells are aligned end-to-end and side-by-side. The latter is often accomplished in the following manner: two cells in end-to-end contact form as crescent-shaped free space with their polar extensions; a neighboring spindle-shaped cell then settles in this space. An arrangement of cells such that their greatest cytoplasmic widths lie at the same level can also be seen. During the recording period, two cells in one of the groups were replicating. One of them realized karyo- and cytokinesis in approximately 80min. The daughter cells moved apart in opposite directions, but never lost contact to the aggregate. This observation shows that contact between presumptive myoblasts and myoblasts is established.