Skip to main content
Immunology logoLink to Immunology
. 1988 Jan;63(1):37–42.

Kinetics of MHC gene expression and mRNA synthesis in brain endothelium.

D Male 1, G Pryce 1
PMCID: PMC1454708  PMID: 3123371

Abstract

Rat brain endothelium was examined in vitro to determine the sequence of events in MHC gene activation following IFN-gamma stimulation. The cell-triggering time, kinetics of mRNA synthesis, rate of MHC induction and rate of decay were measured by quantifying cell-surface MHC expression in the presence or absence of alpha-amanitin. Enhanced class I expression is triggered immediately after IFN-gamma stimulation, and is maximally induced by 4 hr of stimulation. New class I mRNA synthesis starts immediately and proceeds over the next 24 hr. This is followed by increased expression of class I molecules, which reaches plateau levels by 24 hr. While IFN-gamma is present, enhanced class I expression is maintained at 140-200% of that seen on resting cells. On removal of IFN-gamma, class I expression decays towards the levels seen on resting cells, with a half-life of approximately 40 hr. Class II molecules can be induced on these cells as well, but it requires the continuous presence of higher levels of IFN-gamma for more than 48 hr to trigger the cells. Induced class II molecules start to appear 2 days after pulsing and continue to increase until Day 4. If the IFN-gamma is removed from the cultures, class II expression declines rapidly towards zero, with a half-life of approximately 30 hr.

Full text

PDF
37

Selected References

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

  1. Cavender D. E., Haskard D. O., Joseph B., Ziff M. Interleukin 1 increases the binding of human B and T lymphocytes to endothelial cell monolayers. J Immunol. 1986 Jan;136(1):203–207. [PubMed] [Google Scholar]
  2. Craggs R. I., Webster H. D. Ia antigens in the normal rat nervous system and in lesions of experimental allergic encephalomyelitis. Acta Neuropathol. 1985;68(4):263–272. doi: 10.1007/BF00690828. [DOI] [PubMed] [Google Scholar]
  3. Fontana A., Fierz W. The endothelium--astrocyte immune control system of the brain. Springer Semin Immunopathol. 1985;8(1-2):57–70. doi: 10.1007/BF00197247. [DOI] [PubMed] [Google Scholar]
  4. Fukumoto T., McMaster W. R., Williams A. F. Mouse monoclonal antibodies against rat major histocompatibility antigens. Two Ia antigens and expression of Ia and class I antigens in rat thymus. Eur J Immunol. 1982 Mar;12(3):237–243. doi: 10.1002/eji.1830120313. [DOI] [PubMed] [Google Scholar]
  5. Giulian D., Baker T. J., Shih L. C., Lachman L. B. Interleukin 1 of the central nervous system is produced by ameboid microglia. J Exp Med. 1986 Aug 1;164(2):594–604. doi: 10.1084/jem.164.2.594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Goldstein G. W., Betz A. L., Bowman P. D. Use of isolated brain capillaries and cultured endothelial cells to study the blood-brain barrier. Fed Proc. 1984 Feb;43(2):191–195. [PubMed] [Google Scholar]
  7. Hickey W. F., Gonatas N. K., Kimura H., Wilson D. B. Identification and quantitation of T lymphocyte subsets found in the spinal cord of the Lewis rat during acute experimental allergic encephalomyelitis. J Immunol. 1983 Dec;131(6):2805–2809. [PubMed] [Google Scholar]
  8. Hughes C. C., Lantos P. L. Brain capillary endothelial cells in vitro lack surface IgG Fc receptors. Neurosci Lett. 1986 Jul 11;68(1):100–106. doi: 10.1016/0304-3940(86)90237-5. [DOI] [PubMed] [Google Scholar]
  9. Male D. K., Pryce G., Hughes C. C. Antigen presentation in brain: MHC induction on brain endothelium and astrocytes compared. Immunology. 1987 Mar;60(3):453–459. [PMC free article] [PubMed] [Google Scholar]
  10. McCarron R. M., Kempski O., Spatz M., McFarlin D. E. Presentation of myelin basic protein by murine cerebral vascular endothelial cells. J Immunol. 1985 May;134(5):3100–3103. [PubMed] [Google Scholar]
  11. Pober J. S., Gimbrone M. A., Jr, Cotran R. S., Reiss C. S., Burakoff S. J., Fiers W., Ault K. A. Ia expression by vascular endothelium is inducible by activated T cells and by human gamma interferon. J Exp Med. 1983 Apr 1;157(4):1339–1353. doi: 10.1084/jem.157.4.1339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sakai K., Tabira T., Endoh M., Steinman L. Ia expression in chronic relapsing experimental allergic encephalomyelitis induced by long-term cultured T cell lines in mice. Lab Invest. 1986 Mar;54(3):345–352. [PubMed] [Google Scholar]
  13. Sedgwick J. D., Mason D. W. The mechanism of inhibition of experimental allergic encephalomyelitis in the rat by monoclonal antibody against CD4. J Neuroimmunol. 1986 Dec;13(2):217–232. doi: 10.1016/0165-5728(86)90066-4. [DOI] [PubMed] [Google Scholar]
  14. Sobel R. A., Blanchette B. W., Bhan A. K., Colvin R. B. The immunopathology of experimental allergic encephalomyelitis. II. Endothelial cell Ia increases prior to inflammatory cell infiltration. J Immunol. 1984 May;132(5):2402–2407. [PubMed] [Google Scholar]
  15. Traugott U., Raine C. S., McFarlin D. E. Acute experimental allergic encephalomyelitis in the mouse: immunopathology of the developing lesion. Cell Immunol. 1985 Mar;91(1):240–254. doi: 10.1016/0008-8749(85)90047-4. [DOI] [PubMed] [Google Scholar]
  16. Traugott U., Scheinberg L. C., Raine C. S. On the presence of Ia-positive endothelial cells and astrocytes in multiple sclerosis lesions and its relevance to antigen presentation. J Neuroimmunol. 1985 Apr;8(1):1–14. doi: 10.1016/s0165-5728(85)80043-6. [DOI] [PubMed] [Google Scholar]
  17. Vass K., Lassmann H., Wekerle H., Wisniewski H. M. The distribution of Ia antigen in the lesions of rat acute experimental allergic encephalomyelitis. Acta Neuropathol. 1986;70(2):149–160. doi: 10.1007/BF00691433. [DOI] [PubMed] [Google Scholar]
  18. Vass K., Lassmann H., Wisniewski H. M., Iqbal K. Ultracytochemical distribution of myelin basic protein after injection into the cerebrospinal fluid. Evidence for transport through the blood-brain barrier and binding to the luminal surface of cerebral veins. J Neurol Sci. 1984 Mar;63(3):423–433. doi: 10.1016/0022-510x(84)90165-5. [DOI] [PubMed] [Google Scholar]
  19. Wagner C. R., Vetto R. M., Burger D. R. The mechanism of antigen presentation by endothelial cells. Immunobiology. 1984 Dec;168(3-5):453–469. doi: 10.1016/S0171-2985(84)80130-8. [DOI] [PubMed] [Google Scholar]
  20. Willenborg D. O., Sjollema P., Danta G. Immunoregulation of passively induced allergic encephalomyelitis. J Immunol. 1986 Mar 1;136(5):1676–1679. [PubMed] [Google Scholar]
  21. Yu C. L., Haskard D. O., Cavender D., Johnson A. R., Ziff M. Human gamma interferon increases the binding of T lymphocytes to endothelial cells. Clin Exp Immunol. 1985 Dec;62(3):554–560. [PMC free article] [PubMed] [Google Scholar]
  22. van der Meide P. H., Dubbeld M., Vijverberg K., Kos T., Schellekens H. The purification and characterization of rat gamma interferon by use of two monoclonal antibodies. J Gen Virol. 1986 Jun;67(Pt 6):1059–1071. doi: 10.1099/0022-1317-67-6-1059. [DOI] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES