By J. Cervós-Navarro, J. Artigas, B. J. Mršulja (auth.), Prof. Dr. Konstantin-Alexander Hossmann, Dr. Igor Klatzo (eds.)
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Additional info for Cerebrovascular Transport Mechanisms: International Congress of Neuropathology, Vienna, September 5–10, 1982
8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. Anders JJ, Brightman MW (1979) Assemblies of particles in the cell membranes of developing, mature and reactive astrocytes. J Neurocytol 8:777-795 Anders JJ, Brightman MW (1981) lnitial changes in astrocytic membranes at the site of injury to the central nervous system. Anatomical Record 199, 9A (Abstract) Beggs JL, Waggener JO (1976) Transendothelial vesicular transport of protein following compression injury to the spinal cord. Lab lnvest 34:428-439 Bodenheimer TS, Brightman MW (1968) A blood-brain barrier to peroxidase in capillar'ies surrounded by perivascular spaces, Am J Anat 122:249-267 Bordi C, Perrelet A (1978) Orthogonal arrays of particles in plasma membranes of the gastric parietal cell.
In this adjacent gyrus, there were no leaking vessels, and most probably, resorption of the extravasated edematous fluid occurs through various pathways, including drainage by microvessels. In this area we observed the appearance of the positive re action for AP (and also NDPas~ on the abluminal surface of ECs and also in the area of the basement membrane of microvessels (Figs. 14 and 15). This changed localization of the enzymatic activity could be interpreted as an evidence of changed functional polarity of the EC.
Acid phosphatase is present in primary lysosomes of endothelial cells; alkaline phosphatase activity is seen mainly on the plasma membrane of the luminal side but also in the basal la~ina. The latter is also active concerning S'nucleotidase. Butyrylcholinesterase is an enzyme synthesized by most brain capillary endothelial cells, as can be seen by intensive staining of endoplasmic reticulum cisternae. In contrast acetylcholinesterase activity at the capillaries presumably is of neuronal origin.