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Quantitative detection of blood-brain barrier-associated enzymes in cultured endothelial cells of procine brain microvessels

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Summary

The present study deals with a rapid and convenient assay for blood-brain barrier (BBB)-associated enzymes, γ-glutamyl transpeptidase (γ-GTP) and alkaline phosphatase (ALP), in cultured endothelial cells and other cells. These enzyme activities in cultured cells could be efficiently measured by direct incubation of each substrate in the culture plates without pretreatment of the cells. This new direct in situ-in plate assay was more rapid and convenient than conventional ex-plate assays, and these assays gave similar values for specific enzyme activities. γ-GTP and ALP activities could be detected by this in situ method in primary-cultured endothelial cells of porcine brain microvessels, but their levels were lower than those before culture. The degree of loss due to culture differed, between γ-GTP and ALP; a relatively large amount of ALP remained but the γ-GTP level decreased greatly In this direct in situ-in plate assay, cultured porcine aortic endothelial cells exhibited negligibly small activities for both enzymes, whereas cultured astroglial cells of neonatal porcine brain showed moderate γ-GTP activity and a trace of ALP activity. This direct in situ-in plate assay can be used for microculture and automatic measurement and offers a convenient means for studying the possible regulatory mechanisms of the expression of the BBB-associated enzymes.

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References

  1. Adams, S. E.; Bishop, E. J.; Melnykovych, G. Elevation of alkaline phosphatase by retinol in bovine endothelial cells and its possible relationship to lipid biosynthesis. Biochim. Biophys. Acta 885:146–153; 1986.

    Article  PubMed  CAS  Google Scholar 

  2. Arthur, F. E.; Shivers, R. R.; Bowman, P. D. Astrocytemediated induction of tight junctions in brain capillary endothelium: an efficient in vitro model. Dev. Brain Res. 36:155–159; 1987.

    Article  Google Scholar 

  3. Baranczyk-Kuzma, A.; Audus, K. L.; Borchardt, R. T. Catecholamine-metabolizing enzymes of bovine brain microvessel endothelial cell monolayers. J. Neurochem. 46:1956–1960; 1986.

    Article  PubMed  CAS  Google Scholar 

  4. Bates, I. P. The blood-brain barrier and central nervous system drug penetration. Pharm. J. 232:265–268; 1984.

    Google Scholar 

  5. Beck, D. W.; Roberts, R.L.; Olson, J. J. Glial cells influence membrane-associated enzyme activity at the blood-brain barrier. Brain Res. 381:131–137; 1986.

    Article  PubMed  CAS  Google Scholar 

  6. Bowman, P. D.; Betz, A. L.; Ar, D., et al. Primary culture of capillary endothelium from rat brain. In Vitro 17:353–362; 1981.

    Article  PubMed  CAS  Google Scholar 

  7. Bowman, P. D.; Betz, A. L.; Goldstein, G. W. Primary culture of microvascular endothelial cells from bovine retina: selective growth using fibronectin coated substrate and plasma derived serum. In Vitro 18:626–632; 1982.

    PubMed  CAS  Google Scholar 

  8. Cardelli-Cangiano, P.; Fiori, A.; Cangiano, C., et al. Isolated brain microvessels as in vitro equivalents of the blood-brain barrier: selective removal by collagenase of the A-system of neutral amino acid transport. J. Neurochem. 49:1667–1675; 1987.

    Article  PubMed  CAS  Google Scholar 

  9. Caspers, M. L.; Diglio, C. A. Expression of γ-glutamyltranspeptidase in a transformed rat cerebral endothelial cell lien. Biochim. Biophys. Acta 803:1–6; 1984.

    Article  PubMed  CAS  Google Scholar 

  10. DeBault, L. E.; Kahn, L. E.; Frommes, S. P., et al. Cerebral microvessels and derived cells in tissue culture: isolation and preliminary characterization. In Vitro 15:473–487; 1979.

    Article  PubMed  CAS  Google Scholar 

  11. DeBault, L. E.; Cancilla, P. A. Induction of γ-glutamyl transpeptidase in isolated cerebral endothelial cells. Adv. Exp. Med. Biol. 131:79–88; 1980.

    PubMed  CAS  Google Scholar 

  12. DeBault, L. E.; Cancilla, P. A. γ-Glutamyl transpeptidase in isolated brain endothelial cells: induction by glial cells in vitro. Science 207:653–655; 1980.

    Article  PubMed  CAS  Google Scholar 

  13. Diglio, C. A.; Grammas, P.; Giacomelli, F., et al. Primary culture of rat cerebral microvascular endothelial cells. Isolation, growth, and characterization. Lab. Invest. 46:554–563; 1982.

    PubMed  CAS  Google Scholar 

  14. Djuricic, B. M.; Mrsulja B. B. Enzymic activity of the brain: microvessels vs. total forebrain homogenate. Brain Res. 138:561–564; 1977.

    Article  PubMed  CAS  Google Scholar 

  15. Edwards, A. M.; Baddams, H. M.; Lucas, C. M. Two distinct mechanisms for regulation of γ-glutamyl transpeptidase in cultured rathepatocytes by glucocorticoid-like steroids. Biochem. Pharmacol. 36:1223–1230; 1987.

    Article  PubMed  CAS  Google Scholar 

  16. Farley, J. R.; Kyeyune-Nyombi, E.; Tarbaux, N., et al. Alkaline phosphatase activity from human osteosarcoma cell line SaOS-2: an isoenzyme standard for quantifying skeletal alkaline phosphatase activity in serum. Clin. Chem. 35:223–229; 1989.

    PubMed  CAS  Google Scholar 

  17. Frangakis, M. V.; Kimelberg, H. K. Dissociation of neonatal rat brain by dispase for preparation of primary astrocyte cultures. Neurochem. Res. 9:1689–1698; 1984.

    Article  PubMed  CAS  Google Scholar 

  18. Ghandour, M. S.; Langley, O. K.; Varga, V. Immunohistological localization of γ-glutamyltranspeptidase in cerebellum at light and electron microscope levels. Neuroscie Lett. 20:125–129; 1980.

    Article  CAS  Google Scholar 

  19. Goetz, I.; Warren, J.; Estrada, C., et al. Long-term serial cultivation of arterial and capillary endothelium from adult bovine brain. In Vitro Cell. Dev. Biol. 21:172–180; 1985.

    Article  PubMed  CAS  Google Scholar 

  20. Goldstien, G. W.; Betz, A. I. The blood-brain barrier. Sci. Am. 254:74–83; 1986.

    Article  Google Scholar 

  21. Goldstein, G. W. Endothelial cell-astrocyte interactions. A cellular model of the blood-brain barrier. Ann. NY Acad. Sci. 529:31–39; 1988.

    Article  PubMed  CAS  Google Scholar 

  22. Hashimoto, N.; Zubler, R. H. Colorimetric B cell proliferation in the presence of other cell types. J. Immunol. Methods. 90:97–103; 1986.

    Article  PubMed  CAS  Google Scholar 

  23. Hatzinger, P. B.; Stevens, J. L. Rat kidney proximal tubule cells in defined medium: the roles of cholera toxin, extracellular calcium and serum in cell growth and expression of γ-glutamyltranspeptidase. In Vitro Cell. Dev. Biol. 25:205–212; 1989.

    PubMed  CAS  Google Scholar 

  24. Huschtscha, L. I.; Lucibello, F. C.; Bodmer, W. F. A rapid micro method for counting cells “in situ” using a fluorogenic alkaline phosphatase enzyme assay. In Vitro Cell. Dev. Biol. 25:105–108; 1989.

    PubMed  CAS  Google Scholar 

  25. Janzer, R. C.; Raff, M. C. Astrocytes induce, blood-brain barrier properties in endothelial cells. Nature 325:253–257; 1987.

    Article  PubMed  CAS  Google Scholar 

  26. Lasbennes, F.; Gayet, J. Capacity for energy metabolism in microvessels isolated from rat brain. Neurochem. Res. 9:1–10; 1984.

    Article  PubMed  CAS  Google Scholar 

  27. Lowry, O.; Rosebrough, N. J.; Farr, A. L., et al. Protein measurements with the folin phenol reagent. J. Biol. Chem. 193:265–275; 1951.

    PubMed  CAS  Google Scholar 

  28. McCall, A. L.; Valente, J.; Cordero, R., et al. Metabolic characterization of isolated cerebral microvessels: ATP and ADP concentrations. Microvasc. Res. 35:325–333; 1988.

    Article  PubMed  CAS  Google Scholar 

  29. Maxwell, K.; Berliner, J. A.; Cancilla, P. A. Induction of γ-glutamyl transpeptidase in cultured cerebral endothelial cells by a product released by astrocytes. Brain Res. 410:309–314; 1987.

    Article  PubMed  CAS  Google Scholar 

  30. Maxwell, K.; Berliner, J. A.; Cancilla, P. A. Stimulation of glucose analogue uptake by cerebral mierovessel endothelial cells by a product released by astrocytes. J. Neuropathol. Exp. Neurol. 48:69–80; 1989.

    PubMed  CAS  Google Scholar 

  31. Meister, A.; Tate, S. S.; Griffith, O. W. γ-Glutamyl transpeptidase. Methods Enzymol. 77:237–253; 1981.

    Article  PubMed  CAS  Google Scholar 

  32. Mischeck, U.; Meyer, J.; Galla, H. J. Characterization of γ-glutamyl transpeptidase activity ofcultured endothelial cells from porcine brain capillaries. Cell Tissue Res. 256:221–226; 1989.

    Article  PubMed  CAS  Google Scholar 

  33. Orlowski, M.; Sessa, G.; Green, J. P. γ-Glutamyl transpeptidase in brain capillaries: possible site of a blood-brain barrier for amino acids. Science 184:66–68; 1974.

    Article  PubMed  CAS  Google Scholar 

  34. Pardridge, W. M.; Oldendorf, W. W.; Cancilla, P. A., et al. Blood-brain barrier: interface between internal medicine and the brain. Ann. Intern. Med. 105:82–85; 1986.

    PubMed  CAS  Google Scholar 

  35. Pardridge, W. M. Recent advances in blood-brain barrier transport. Ann. Rev. Pharmacol. Toxicol. 28:25–39; 1988.

    Article  CAS  Google Scholar 

  36. Rabito, C. A.; Kreisberg, J. I.; Wight, D. Alkaline phosphatase and γ-glutamyl transpeptidase as polarization markers during the organization of LLC-PK1 cells into an epithelial membrane. J. Biochem. Chem. 259:574–582; 1984.

    CAS  Google Scholar 

  37. Reese, T. S.; Karnovsky, M. J. Fine structural localization of blood-brain barrier to exogeneous peroxidase. J. Cell Biol. 34:207–217; 1967.

    Article  PubMed  CAS  Google Scholar 

  38. Reyes, E.; Lewis, L.; Saland, L. Isolation of γ-glutamyl transpeptidase from glial cells. Proc. West. Pharmacol. Soc. 23:381–383; 1980.

    PubMed  CAS  Google Scholar 

  39. Rutenburg, A. M.; Kim, H.; Fischbein, J. W., et al. Histochemical and ultrastructural demonstration of γ-glutamyl transpeptidase activity. J. Histochem. Cytochem. 17:517–526; 1969.

    PubMed  CAS  Google Scholar 

  40. Santoso, A. W. B.; Bar, T. Postnatal development of γ-GT activity in rat brain microvessels corresponds to capillary growth and differentiation. Int. J. Dev. Neurosci. 4:503–511; 1986.

    Article  CAS  Google Scholar 

  41. Sensenbrenner, M. G.; Bock, D. E.; Porte, A. Biochemical and ultrastructural studies of cultured rat astroglial cells—effect of brain extract and dBcAMP on glial fibrillary acidic protein and glial filaments. Differentiation 17:51–61; 1980.

    Article  PubMed  CAS  Google Scholar 

  42. Shine, H. D.; Haber, B. Immunocytochemical localization of γ-glutamyl transpeptidase in the rat CNS. Brain Res. 217:339–349; 1981.

    Article  PubMed  CAS  Google Scholar 

  43. Shine, H. D.; Hertz, L.; deVellis, J., et al. A fluorometric assay for γ-glutamyl transpeptidase: demonstration of enzymatic activity in cultured cells of neural orgin. Neurochem. Res. 6:453–463; 1981.

    Article  PubMed  CAS  Google Scholar 

  44. States, B.; Segal, S. Characterization of γ-glutamyltranspeptidase in cultured skin fibroblasts from normals and cystinotics. Enzyme 26:156–164; 1981.

    PubMed  CAS  Google Scholar 

  45. Stewart, P. A.; Wiley, M. J. Developing nervous tissue induces formation of blood-brain barrier characteristics in invading endothelial cells: a study using quail-chick transplantation chimeras. Dev. Biol. 84:183–192; 1981.

    Article  PubMed  CAS  Google Scholar 

  46. Tao-Cheng, J.; Nagy, Z.; Brightman, M. W., Tight junctions of brain endothelium in vitro are enhanced by astroglia. J. Neurosci. 7:3293–3299; 1987.

    PubMed  CAS  Google Scholar 

  47. Taylor-Robinson, D.; Addey, J. P. Comparison of techniques for the isolation of T-strain mycoplamas. Nature 222:274–275; 1969.

    Article  PubMed  CAS  Google Scholar 

  48. Tontsch, U.; Bauer, H. Isolation, characterization, and long-term cultivation of porcine and murine cerebral capillary endothelial cells. Microvasc. Res. 37:148–161; 1989.

    Article  PubMed  CAS  Google Scholar 

  49. Vorbrodt, A. W.; Lossinsky, A. S.; Wisniewski, H. M. Enzyme cytochemistry of blood-brain barrier (BBB) disturbances. Act. Neuropathol. Suppl. VIII:43–57; 1983.

    Google Scholar 

  50. Vorbrodt, A. W. Ultrastructural cytochemistry of blood-brain barrier endothelial. Prog. Histochem. Cytochem. 18:1–99; 1988.

    PubMed  CAS  Google Scholar 

  51. Wey, H. E.; Jakubowski, J. A.; Deykin, D. Incorporation and redistribution of arachidonic acid in diacyl and ether phospholipids of bovine aortic endothelial cells. Biochim. Biophys. Acta. 878:380–386; 1986.

    PubMed  CAS  Google Scholar 

  52. Williams, S. K.; Gillis, J. F.; Matthews, M. A., et al. Isolation and characterization of brain endothelial cells: morphology and enzymatic activity. J. Neurochem. 35:374–381; 1980.

    Article  PubMed  CAS  Google Scholar 

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Fukushima, H., Fujimoto, M. & Ide, M. Quantitative detection of blood-brain barrier-associated enzymes in cultured endothelial cells of procine brain microvessels. In Vitro Cell Dev Biol 26, 612–620 (1990). https://doi.org/10.1007/BF02624211

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