Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1982 May 1;93(2):357–364. doi: 10.1083/jcb.93.2.357

Histamine receptors of the microvascular endothelium revealed in situ with a histamine-ferritin conjugate: characteristic high-affinity binding sites in venules

PMCID: PMC2112850  PMID: 7201474

Abstract

Histamine covalently bound to glutaraldehyde-activated ferritin was prepared as either monomers or as small aggregates of approximately 0.05 to 0.15 micrometer Diam, suitable for electron microscopic detection of histamine cellular binding sites. The histamine-ferritin conjugates (MF) maintain the histamine capability to induce the opening of endothelial junctions in venules. To investigate the distribution of histamine receptors in the vascular endothelium, monomers or aggregates of MF were perfused in situ (mice), and various vascular beds, particularly that of the diaphragm, were fixed and processed for electron microscopy. The conjugate was preferentially bound on restricted areas of luminal endothelial cell plasmalemma especially in regions rich in filaments, and near the junctions between endothelial cells. The density of histamine binding sites was characteristically high in venules; it occurred to a much lesser extent in arterioles, veins, and muscular arteries whereas capillaries and aorta showed the lowest values. A similar distribution was obtained after perfusion of H1 or H2 receptor agonists coupled to ferritin (2-pyridylethylamine- ferritin [PF], or 4-methylhistamine-ferritin [MF], respectively). The binding specificity was assessed through control experiments with either native or activated ferritin or by competition with histamine. The findings suggest that histamine receptors are largely represented in the cell membrane of the vascular endothelium, particularly in venules. Experiments using specific H1 and H2 receptor agonists (PF and MF) and antagonists (mepyramine and cimetidine) indicate that the venular endothelium contains mainly H2 receptors.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

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

  1. Altura B. M. Pharmacology of venular smooth muscle: new insights. Microvasc Res. 1978 Jul;16(1):91–117. doi: 10.1016/0026-2862(78)90047-x. [DOI] [PubMed] [Google Scholar]
  2. Arosio P., Adelman T. G., Drysdale J. W. On ferritin heterogeneity. Further evidence for heteropolymers. J Biol Chem. 1978 Jun 25;253(12):4451–4458. [PubMed] [Google Scholar]
  3. Arturson G. Microvascular permeability to macromolecules in thermal injury. Acta Physiol Scand Suppl. 1979;463:111–122. [PubMed] [Google Scholar]
  4. Barer G. R., Emery C. J., Mohammed F. H., Mungall I. P. H1 and H2 histamine actions on lung vessels; their relevance to hypoxic vasoconstriction. Q J Exp Physiol Cogn Med Sci. 1978 Apr;63(2):157–169. doi: 10.1113/expphysiol.1978.sp002428. [DOI] [PubMed] [Google Scholar]
  5. Beaven M. A. Histamine (second of two parts). N Engl J Med. 1976 Feb 5;294(6):320–325. doi: 10.1056/NEJM197602052940608. [DOI] [PubMed] [Google Scholar]
  6. Berner P. F., Disalvo J., Schwartz A. Differential inhibitory effects of the ionophore RO2-2985 (X537A) on contractile responses to potassium and histamine in coronary artery smooth muscle. J Pharmacol Exp Ther. 1980 Apr;213(1):59–63. [PubMed] [Google Scholar]
  7. Bhargava K. P., Nath R., Palit G. Nature of histamine receptors concerned in capillary permeability. Br J Pharmacol. 1977 Feb;59(2):349–351. doi: 10.1111/j.1476-5381.1977.tb07499.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Black J. W., Duncan W. A., Durant C. J., Ganellin C. R., Parsons E. M. Definition and antagonism of histamine H 2 -receptors. Nature. 1972 Apr 21;236(5347):385–390. doi: 10.1038/236385a0. [DOI] [PubMed] [Google Scholar]
  9. Buonassisi V., Venter J. C. Hormone and neurotransmitter receptors in an established vascular endothelial cell line. Proc Natl Acad Sci U S A. 1976 May;73(5):1612–1616. doi: 10.1073/pnas.73.5.1612. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Chipman P., Glover W. E. Histamine H2-receptors in the human peripheral circulation. Br J Pharmacol. 1976 Apr;56(4):494–496. doi: 10.1111/j.1476-5381.1976.tb07463.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dey S. K., Villanueva C., Abdou N. I. Histamine receptors on rabbit blastocyst and endometrial cell membranes. Nature. 1979 Apr 12;278(5705):648–649. doi: 10.1038/278648a0. [DOI] [PubMed] [Google Scholar]
  12. Durant G. J., Ganellin C. R., Parsons M. E. Chemical differentiation of histamine H1- and H2-receptor agonists. J Med Chem. 1975 Sep;18(9):905–909. doi: 10.1021/jm00243a009. [DOI] [PubMed] [Google Scholar]
  13. Greaves M. W., Marks R., Robertson I. Subclassses of histamine receptors on human skin blood vessels and their possible clinical significance [proceedings]. Br J Clin Pharmacol. 1977 Oct;4(5):657P–657P. doi: 10.1111/j.1365-2125.1977.tb00829.x. [DOI] [PubMed] [Google Scholar]
  14. Guth P. H., Moler T. L., Smith E. H1 and H2 histamine receptors in rat gastric submocosal arterioles. Microvasc Res. 1980 May;19(3):320–328. doi: 10.1016/0026-2862(80)90051-5. [DOI] [PubMed] [Google Scholar]
  15. Hiley C. R., Wilson H., Yates M. S. Identification of beta-adrenoceptors and histamine receptors in the cat nasal vasculature. Acta Otolaryngol. 1978 May-Jun;85(5-6):444–448. [PubMed] [Google Scholar]
  16. Hirschowitz B. I. H-2 histamine receptors. Annu Rev Pharmacol Toxicol. 1979;19:203–244. doi: 10.1146/annurev.pa.19.040179.001223. [DOI] [PubMed] [Google Scholar]
  17. Ichikawa I., Brenner B. M. Mechanisms of action of hisamine and histamine antagonists on the glomerular microcirculation in the rat. Circ Res. 1979 Dec;45(6):737–745. doi: 10.1161/01.res.45.6.737. [DOI] [PubMed] [Google Scholar]
  18. Johnson C. L., Weinstein H., Green J. P. Studies on histamine H2 receptors coupled to cardiac adenylate cyclase. Effects of guanylnucleotides and structural requirements for agonist activity. Biochim Biophys Acta. 1979 Oct 4;587(2):155–168. doi: 10.1016/0304-4165(79)90350-7. [DOI] [PubMed] [Google Scholar]
  19. Karnushina I. L., Palacios J. M., Barbin G., Dux E., Joó F., Schwartz J. C. Studies on a capillary-rich fraction isolated from brain: histaminic components and characterization of the histamine receptors linked to adenylate cyclase. J Neurochem. 1980 May;34(5):1201–1208. doi: 10.1111/j.1471-4159.1980.tb09960.x. [DOI] [PubMed] [Google Scholar]
  20. Kishida Y., Olsen B. R., Berg R. A., Prockop D. J. Two improved methods for preparing ferritin-protein conjugates for electron microscopy. J Cell Biol. 1975 Feb;64(2):331–339. doi: 10.1083/jcb.64.2.331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. MAJNO G., PALADE G. E. Studies on inflammation. 1. The effect of histamine and serotonin on vascular permeability: an electron microscopic study. J Biophys Biochem Cytol. 1961 Dec;11:571–605. doi: 10.1083/jcb.11.3.571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Majno G., Gilmore V., Leventhal M. On the mechanism of vascular leakage caused by histaminetype mediators. A microscopic study in vivo. Circ Res. 1967 Dec;21(6):833–847. doi: 10.1161/01.res.21.6.833. [DOI] [PubMed] [Google Scholar]
  23. Majno G., Shea S. M., Leventhal M. Endothelial contraction induced by histamine-type mediators: an electron microscopic study. J Cell Biol. 1969 Sep;42(3):647–672. doi: 10.1083/jcb.42.3.647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Maylié-Pfenninger M. F., Jamieson J. D. Distribution of cell surface saccharides on pancreatic cells. I. General method for preparation and purification of lectins and lectin-ferritin conjugates. J Cell Biol. 1979 Jan;80(1):69–76. doi: 10.1083/jcb.80.1.69. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Melmon K. L., Bourne H. R., Weinstein J., Sela M. Receptors for histamine can be detected on the surface of selected leukocytes. Science. 1972 Aug 25;177(4050):707–709. doi: 10.1126/science.177.4050.707. [DOI] [PubMed] [Google Scholar]
  26. Osband M., McCaffrey R. Solubilization, separation, and partial characterization of histamine H1 and H2 receptors from calf thymocyte membranes. J Biol Chem. 1979 Oct 25;254(20):9970–9972. [PubMed] [Google Scholar]
  27. Payne J. W. Polymerization of proteins with glutaraldehyde. Soluble molecular-weight markers. Biochem J. 1973 Dec;135(4):867–873. doi: 10.1042/bj1350867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Reinhardt D., Ritter E. Hypothermia-induced potentiation of histamine H2-receptor-mediated relaxation and cyclic AMP increase in the isolated mesenteric artery of the rabbit. Agents Actions. 1979 Apr;9(1):9–14. doi: 10.1007/BF02024089. [DOI] [PubMed] [Google Scholar]
  29. Reite O. B. Comparative physiology of histamine. Physiol Rev. 1972 Jul;52(3):778–819. doi: 10.1152/physrev.1972.52.3.778. [DOI] [PubMed] [Google Scholar]
  30. SCHAYER R. W. Evidence that induced histamine is an intrinsic regulator of the microcirculatory system. Am J Physiol. 1962 Jan;202:66–72. doi: 10.1152/ajplegacy.1962.202.1.66. [DOI] [PubMed] [Google Scholar]
  31. Schwaiger M., Jacobson E. D. Peripheral vascular H2 receptors to histamine. Circ Shock. 1979;6(3):213–221. [PubMed] [Google Scholar]
  32. Simionescu N., Simionescu M., Palade G. E. Structural basis of permeability in sequential segments of the microvasculature of the diaphragm. I. Bipolar microvascular fields. Microvasc Res. 1978 Jan;15(1):1–16. doi: 10.1016/0026-2862(78)90001-8. [DOI] [PubMed] [Google Scholar]
  33. Simionescu N., Simionescu M., Palade G. E. Structural basis of permeability in sequential segments of the microvasculature of the diaphragm. II. Pathways followed by microperoxidase across the endothelium. Microvasc Res. 1978 Jan;15(1):17–36. doi: 10.1016/0026-2862(78)90002-x. [DOI] [PubMed] [Google Scholar]
  34. Suran A. A., Tarver H. Heterogeneity of horse spleen ferritin and apoferritin: comparison of electrophoretic and chromatographic fractions. Arch Biochem Biophys. 1965 Aug;111(2):399–406. doi: 10.1016/0003-9861(65)90202-x. [DOI] [PubMed] [Google Scholar]
  35. Tran V. T., Chang R. S., Snyder S. H. Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6290–6294. doi: 10.1073/pnas.75.12.6290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Uchida M., Takagi K. Purification of histamine receptor, (III) Characterization of receptor rich membrane fraction of small intestinal smooth muscle of the cat. Jpn J Pharmacol. 1977 Feb;27(1):1–7. doi: 10.1254/jjp.27.1. [DOI] [PubMed] [Google Scholar]
  37. VANE J. R. A sensitive method for the assay of 5-hydroxytryptamine. Br J Pharmacol Chemother. 1957 Sep;12(3):344–349. doi: 10.1111/j.1476-5381.1957.tb00146.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Wahl M., Kuschinsky W. The dilating effect of histamine on pial arteries of cats and its mediation by H2 receptors. Circ Res. 1979 Feb;44(2):161–165. doi: 10.1161/01.res.44.2.161. [DOI] [PubMed] [Google Scholar]
  39. Weinstein Y., Melmon K. L., Bourne H. R., Sela M. Specific leukocyte receptors for small endogenous hormones. Detection by cell binding to insolubilized hormone preparations. J Clin Invest. 1973 Jun;52(6):1349–1361. doi: 10.1172/JCI107307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Williams M. A., Harrison P. M. Electron-microscopic and chemical studies of oligomers in horse ferritin. Biochem J. 1968 Nov;110(2):265–280. doi: 10.1042/bj1100265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Zamiri I., Mason J. Electrophoresis of ferritins. Nature. 1968 Jan 20;217(5125):258–259. doi: 10.1038/217258a0. [DOI] [PubMed] [Google Scholar]

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

RESOURCES