Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1967 Jul 1;34(1):207–217. doi: 10.1083/jcb.34.1.207

FINE STRUCTURAL LOCALIZATION OF A BLOOD-BRAIN BARRIER TO EXOGENOUS PEROXIDASE

T S Reese 1, Morris J Karnovsky 1
PMCID: PMC2107213  PMID: 6033532

Abstract

Horseradish peroxidase was administered to mice by intravenous injection, and its distribution in cerebral cortex studied with a recently available technique for localizing peroxidase with the electron microscope. Brains were fixed by either immersion or vascular perfusion 10–60 min after administration of various doses of peroxidase. Exogenous peroxidase was localized in the lumina of blood vessels and in some micropinocytotic vesicles within endothelial cells; none was found beyond the vascular endothelium. Micropinocytotic vesicles were few in number and did not appear to transport peroxidase while tight junctions between endothelial cells were probably responsible for preventing its intercellular passage. Our findings therefore localize, at a fine structural level, a "barrier" to the passage of peroxidase at the endothelium of vessels in the cerebral cortex. The significance of these findings is discussed, particularly with reference to a recent study in which similar techniques were applied to capillaries in heart and skeletal muscle.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brightman M. W. The distribution within the brain of ferritin injected into cerebrospinal fluid compartments. II. Parenchymal distribution. Am J Anat. 1965 Sep;117(2):193–219. doi: 10.1002/aja.1001170204. [DOI] [PubMed] [Google Scholar]
  2. Clawson C. C., Hartmann J. F., Vernier R. L. Electron microscopy of the effect of gram-negative endotoxin on the blood-brain barrier. J Comp Neurol. 1966 Jun;127(2):183–198. doi: 10.1002/cne.901270204. [DOI] [PubMed] [Google Scholar]
  3. DOBBING J. The blood-brain barrier. Physiol Rev. 1961 Jan;41:130–188. doi: 10.1152/physrev.1961.41.1.130. [DOI] [PubMed] [Google Scholar]
  4. DONAHUE S. A RELATIONSHIP BETWEEN FINE STRUCTURE AND FUNCTION OF BLOOD VESSELS IN THE CENTRAL NERVOUS SYSTEM OF RABBIT FETUSES. Am J Anat. 1964 Jul;115:17–26. doi: 10.1002/aja.1001150103. [DOI] [PubMed] [Google Scholar]
  5. FARQUHAR M. G., PALADE G. E. Junctional complexes in various epithelia. J Cell Biol. 1963 May;17:375–412. doi: 10.1083/jcb.17.2.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J Cell Biol. 1965 Jul;26(1):263–291. doi: 10.1083/jcb.26.1.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Goldfischer S., Villaverde H., Forschirm R. The demonstration of acid hydrolase, thermostable reduced diphosphopyridine nucleotide tetrazolium reductase and peroxidase activities in human lipofuscin pigment granules. J Histochem Cytochem. 1966 Sep;14(9):641–652. doi: 10.1177/14.9.641. [DOI] [PubMed] [Google Scholar]
  8. Graham R. C., Jr, Karnovsky M. J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem. 1966 Apr;14(4):291–302. doi: 10.1177/14.4.291. [DOI] [PubMed] [Google Scholar]
  9. Kuffler S. W., Nicholls J. G. The physiology of neuroglial cells. Ergeb Physiol. 1966;57:1–90. [PubMed] [Google Scholar]
  10. LAMPERT P., CARPENTER S. ELECTRON MICROSCOPIC STUDIES ON THE VASCULAR PERMEABILITY AND THE MECHANISM OF DEMYELINATION IN EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS. J Neuropathol Exp Neurol. 1965 Jan;24:11–24. doi: 10.1097/00005072-196501000-00002. [DOI] [PubMed] [Google Scholar]
  11. LeFevre P. G., Peters A. A. Evidence of mediated transfer of monosaccharides from blood to brain in rodents. J Neurochem. 1966 Jan;13(1):35–46. doi: 10.1111/j.1471-4159.1966.tb10282.x. [DOI] [PubMed] [Google Scholar]
  12. MUIR A. R., PETERS A. Quintuple-layered membrane junctions at terminal bars between endothelial cells. J Cell Biol. 1962 Feb;12:443–448. doi: 10.1083/jcb.12.2.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. PAPPENHEIMER J. R. Passage of molecules through capillary wals. Physiol Rev. 1953 Jul;33(3):387–423. doi: 10.1152/physrev.1953.33.3.387. [DOI] [PubMed] [Google Scholar]
  14. Pappenheimer J. R. Cerebral HCO3- transport and control of breathing. Fed Proc. 1966 May-Jun;25(3):884–886. [PubMed] [Google Scholar]
  15. STRAUS W. Colorimetric analysis with N, N-dimethyl-p-phenylenediamine of the uptake of intravenously injected horseradish peroxidase by various tissues of the rat. J Biophys Biochem Cytol. 1958 Sep 25;4(5):541–550. doi: 10.1083/jcb.4.5.541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Shakib M., Cunha-Vaz J. G. Studies on the permeability of the blood-retinal barrier. IV. Junctional complexes of the retinal vessels and their role in the permeability of the blood-retinal barrier. Exp Eye Res. 1966 Jul;5(3):229–234. doi: 10.1016/s0014-4835(66)80011-8. [DOI] [PubMed] [Google Scholar]
  17. VANHARREVELD A., CROWELL J., MALHOTRA S. K. A STUDY OF EXTRACELLULAR SPACE IN CENTRAL NERVOUS TISSUE BY FREEZE-SUBSTITUTION. J Cell Biol. 1965 Apr;25:117–137. doi: 10.1083/jcb.25.1.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES