Bibliothek

Notizen: Summary The nonparenchymal portion of the liver of parasitic adult lampreys (Petromyzon marinus L.) consists of endothelial, Kupffer, fibroblast-like, fat-storing, and granulated cells. The fenestrae of endothelial cells are not organized into sieve plates but are of highly variable size and distribution. The dimension of large molccular size. Small numbers of Kupffer cells possess many features of these cells observed in other vertebrates but they do not have worm-like bodies and endogenous peroxidase activity. They are involved in erythrophagocytosis and perhaps the ingestion of other foreign material but they do not store iron. Fat-storing and fibroblast-like cells share many morphological features and may be different expressions of the same cell type. These perisinusoidal cells are rich in organelles suggesting protein synthesis but the fibroblast-like cells lack fat droplets. A cell with a large Golgi apparatus and associated cytoplasmic granules resembles the pit cell described in the liver of a few other vertebrates. The morphology of nonparenchymal cells of the liver in parasitic adult lampreys does not reflect the absence of bile ducts in this organism.

Notizen: Summary Thin-section and freeze-fracture observations of the plasma membranes of hepatocytes from parasitic adult lampreys, Petromyzon marinus, reveal large (250 nm–4.5 μm diameter) gap junctions of highly irregular configuration. The multiformity of these junctions is partially due to the fact that they follow the contours of the undulating cell surface of the irregularly shaped hepatocytes. In addition, junctional membrane is characterized by a slight “rippling” which is not seen on adjacent non-junctional membrane. Although some annular-shaped junctions are associated to non-junctional membrane, others seem completely internalized and they surround portions of the cytoplasm. In P-face replicas the gap junctions are seen to be composed of closely packed particles of 6.0–6.5 nm diameter. E-face replicas of junctional membrane are relatively smooth, a fact which may be related to the small size of the intramembranous particles. Differences in size and shape of gap junctions in hepatocytes of larval (Peek et al. 1979) and adult lampreys may reflect the absence of bile canaliculi and bile ducts in the adult liver and an increased role of these junctions in co-ordination of an endocrine secretory mechanism.

Notizen: Summary Brain tumors, benign and malignant, are characteristically more permeable to various types of tracer molecules than the neuropil in which they are embedded. Impermeability of brain neuropil capillaries is imparted by the blood-brain barrier, the anatomic basis of which is the network of interendothelial zonulae occludentes that seal capillary endothelial cells. To explore both the vascular elements of brain neoplasms and the route of tracer extravasation from them, as well as the possible effects of brain tumors on the permeability of peritumoral neuropil capillaries, brain tumors were induced in newborn Wistar rats by intracerebral (i.c.) injection of C-6 astrocytoma cells. The protein tracer horseradish peroxidase (HRP) was injected systemically into both normal and tumorbearing rats to mark the pathway along which it flowed into the tumor parenchyma tissue spaces, and to signal any concomitant tracer loss from the tumor extracellular compartment or peritumoral brain capillaries, into the neuropil extracellular milieu. Electron-microscopic examination on thin plastic sections of tumor and peritumoral neuropil revealed massive extravasation of tracer into the tumor tissue spaces, but none was seen outside of the capillaries in the surrounding brain neuropil. Zonulae occludentes of both tumor capillary endothelium and brain capillary endothelium were devoid of tracer and judged tight (sealed). Tracer was seen in pinocytotic vesicles in the highly attenuated endothelium of tumor capillaries and also in cytoplasmic vesicles within the tumor cells. The peritumoral and contralateral neuropil capillary endothelium exhibited reaction product-filled pinocytotic vesicles and vesiculo-tubular conduits. Often, one end of a HRP-filled vesiculo-tubular channel appeared continuous with either the luminal or abluminal plasmalemma. High-voltage electron microscopy of these conduits often showed them to be continuous with both luminal and abluminal surfaces of the endothelium, thus forming a continuum across the capillary wall. In addition, these transendothelial channels, clearly constituted as chains of fused vesicles, were often seen in close proximity to, or fused with, dense bodies in the endothelial cytoplasm. In spite of the presence of HRP-filled structures in the peritumoral neuropil capillary endothelium of tumor-bearing rats, no evidence of tracer extravasation from these vessels was apparent. These results suggest that although peritumoral and contralateral neuropil capillaries possess the machinery for extravasation of tracer, likely as a response to the presence of the neoplasm, tracer is not lost but, instead, is degraded by endothelial enzymes. The extensive flooding of the tumor extracellular compartment with tracer may be achieved by transport of HRP across the very thin walls of tumor capillaries by single cytoplasmic vesicles which structurally and functionally play the role of transendothelial channels. Based on the results of this study, it is unlikely that molecules delivered systemically to treat brain neoplasms, will leak into the peritumor or contralateral neuropil, either from their own capillaries, or from the extracellular compartment of the tumor parenchyma.