The blood-brain barrier in a reptile, Anolis carolinensis

• Published in: Tissue & cell Vol. 6; no. 2; pp. 319 - 333
• Main Authors: Kenny, Terry P., Shivers, Richard R.
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 1974
• Subjects: Animals; Binding Sites; Blood-Brain Barrier; Capillaries - ultrastructure; Capillary Permeability; Endothelium - ultrastructure; Ferritins - metabolism; Lizards - anatomy & histology; Microscopy, Electron; Neurons - ultrastructure; Peroxidases - metabolism
• ISSN: 0040-8166; 1532-3072
• DOI: 10.1016/0040-8166(74)90056-1

An electron microscopic study was made of the ultrastructure and permeability of the capillaries in the cerebral hemispheres of the lizard, Anolis carolinensis. The brain of Anolis is vascularized by a loop-type pattern consisting exclusively of arteriovenous capillary loops. The ultrastructure of the endothelium and the arrangement of the various layers from the capillary lumen to the central nervous tissue is similar to that of mammals. The endothelial cells form a continuous layer around the lumen and are joined by tight interendothelial junctions. The basal lamina of the endothelium is also continuous and encloses pericyte processes. The cells of the nervous tissue rest directly on the basal lamina of the capillary and are separated from each other by a 200 Å space. Intravenously injected horseradish peroxidase (MW 40,000) and ferritin (MW 500,000) were used to study the permeability of the capillaries. The entry of horseradish peroxidase and ferritin into the intercellular spaces of the brain is restricted by the tightness of the interendothelial junctions. No vesicular transport of either tracer occurs; however, ferritin does enter the endothelial cells in vacuoles. No tracer molecules are present in the basal lamina, pericytes, or nervous tissue. The different responses of the endothelial cell to the tracers used in this study suggest that endocytotic activities of endothelial cells involve different processes. Vacuoles formed by marginal folds, vacuoles formed by endothelial surface projections or deep invaginations of the plasma membrane, 600–800 Å vesicles, and coated vesicles all seem to differ in the nature of the substances which they endocytose.