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. 1994;3(3):223–227. doi: 10.1155/S0962935194000323

In vitro Release of Eosinophil Proteins in Allergic and Atopic Dermatitis Patients

L K Poulsen 1,✉, C M Reimert 1, C Bindslev-Jensen 2
PMCID: PMC2367035  PMID: 18472947

Abstract

To investigate whether eosinophils are stimulated in vivo or have acquired an increased susceptibility to stimuli from the coagulation cascade, the release of eosinophil proteins was compared for three groups of donors with different levels of serum IgE. (1) with atopic dermatitis (s-IgE > 5000 IU/ml, n = 11); (2) with inhalant allergy (200 < s-IgE < 2 000 IU/ml, n = 10); and (3) non-allergic (s- IgE < 100 IU/ml, n = 10). The levels of eosinophil cationic protein and eosinophil protein X (ECP, EPX) were determined in serum (clotting time = 2.0 h) and plasma. Serum and plasma ECP in normal donors demonstrated large intra-personal variations (C.V. 50–80%), but serum-ECP (mean 8.1 ng/ml) was clearly distinguishable from plasma ECP (mean 1.0 ng/ml) by a factor of 8 (range: 5.6–11.6). The ECP released during clotting was markedly increased in the atopic dermatitis group (serum:plasma ratio 13.5, p < 0.003) compared with the other groups (6.7 and 5.6). EPX, having a higher plasma level, demonstrated a less pronounced release (serum: plasma ratios 2.0, 1.7 and 1.4), with no statistical difference between donor groups. Considering all donors together the levels of ECP and EPX in plasma and in serum were correlated to the number of eosinophils (coefficients of correlation 0.54-0.58, p < 0.002).

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Selected References

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  1. Ercan Z. S., Soydan A. S., Türker R. K. Possible involvement of endothelium in the responses of various vasoactive agents in rabbit isolated perfused kidney. Gen Pharmacol. 1990;21(2):205–209. doi: 10.1016/0306-3623(90)90902-x. [DOI] [PubMed] [Google Scholar]
  2. Gray G. A., Schott C., Julou-Schaeffer G., Fleming I., Parratt J. R., Stoclet J. C. The effect of inhibitors of the L-arginine/nitric oxide pathway on endotoxin-induced loss of vascular responsiveness in anaesthetized rats. Br J Pharmacol. 1991 May;103(1):1218–1224. doi: 10.1111/j.1476-5381.1991.tb12327.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Guc M. O., Furman B. L., Paratt J. R. Modification of alpha-adrenoceptor-mediated pressor responses by NG-nitro-L-arginine methyl ester and vasopressin in endotoxin-treated pithed rats. Eur J Pharmacol. 1992 Nov 24;224(1):63–69. doi: 10.1016/0014-2999(92)94819-h. [DOI] [PubMed] [Google Scholar]
  4. Ikegawa R., Matsumura Y., Tsukahara Y., Takaoka M., Morimoto S. Phosphoramidon, a metalloproteinase inhibitor, suppresses the secretion of endothelin-1 from cultured endothelial cells by inhibiting a big endothelin-1 converting enzyme. Biochem Biophys Res Commun. 1990 Sep 14;171(2):669–675. doi: 10.1016/0006-291x(90)91198-2. [DOI] [PubMed] [Google Scholar]
  5. Kikeri D., Pennell J. P., Hwang K. H., Jacob A. I., Richman A. V., Bourgoignie J. J. Endotoxemic acute renal failure in awake rats. Am J Physiol. 1986 Jun;250(6 Pt 2):F1098–F1106. doi: 10.1152/ajprenal.1986.250.6.F1098. [DOI] [PubMed] [Google Scholar]
  6. Knowles R. G., Salter M., Brooks S. L., Moncada S. Anti-inflammatory glucocorticoids inhibit the induction by endotoxin of nitric oxide synthase in the lung, liver and aorta of the rat. Biochem Biophys Res Commun. 1990 Nov 15;172(3):1042–1048. doi: 10.1016/0006-291x(90)91551-3. [DOI] [PubMed] [Google Scholar]
  7. Martin W., Villani G. M., Jothianandan D., Furchgott R. F. Selective blockade of endothelium-dependent and glyceryl trinitrate-induced relaxation by hemoglobin and by methylene blue in the rabbit aorta. J Pharmacol Exp Ther. 1985 Mar;232(3):708–716. [PubMed] [Google Scholar]
  8. Matsumura Y., Ikegawa R., Tsukahara Y., Takaoka M., Morimoto S. Conversion of big endothelin-1 to endothelin-1 by two-types of metalloproteinases of cultured porcine vascular smooth muscle cells. Biochem Biophys Res Commun. 1991 Aug 15;178(3):899–905. doi: 10.1016/0006-291x(91)90976-e. [DOI] [PubMed] [Google Scholar]
  9. Meyrick B. O., Ryan U. S., Brigham K. L. Direct effects of E coli endotoxin on structure and permeability of pulmonary endothelial monolayers and the endothelial layer of intimal explants. Am J Pathol. 1986 Jan;122(1):140–151. [PMC free article] [PubMed] [Google Scholar]
  10. Moncada S., Palmer R. M., Higgs E. A. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol Rev. 1991 Jun;43(2):109–142. [PubMed] [Google Scholar]
  11. Morel D. R., Lacroix J. S., Hemsen A., Steinig D. A., Pittet J. F., Lundberg J. M. Increased plasma and pulmonary lymph levels of endothelin during endotoxin shock. Eur J Pharmacol. 1989 Aug 29;167(3):427–428. doi: 10.1016/0014-2999(89)90454-8. [DOI] [PubMed] [Google Scholar]
  12. Okada K., Miyazaki Y., Takada J., Matsuyama K., Yamaki T., Yano M. Conversion of big endothelin-1 by membrane-bound metalloendopeptidase in cultured bovine endothelial cells. Biochem Biophys Res Commun. 1990 Sep 28;171(3):1192–1198. doi: 10.1016/0006-291x(90)90811-z. [DOI] [PubMed] [Google Scholar]
  13. Radomski M. W., Palmer R. M., Moncada S. Glucocorticoids inhibit the expression of an inducible, but not the constitutive, nitric oxide synthase in vascular endothelial cells. Proc Natl Acad Sci U S A. 1990 Dec;87(24):10043–10047. doi: 10.1073/pnas.87.24.10043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Rubanyi G. M., Botelho L. H. Endothelins. FASEB J. 1991 Sep;5(12):2713–2720. doi: 10.1096/fasebj.5.12.1916094. [DOI] [PubMed] [Google Scholar]
  15. Schneider F., Schott C., Stoclet J. C., Julou-Schaeffer G. L-arginine induces relaxation of small mesenteric arteries from endotoxin-treated rats. Eur J Pharmacol. 1992 Feb 11;211(2):269–272. doi: 10.1016/0014-2999(92)90539-g. [DOI] [PubMed] [Google Scholar]
  16. Sugiura M., Inagami T., Kon V. Endotoxin stimulates endothelin-release in vivo and in vitro as determined by radioimmunoassay. Biochem Biophys Res Commun. 1989 Jun 30;161(3):1220–1227. doi: 10.1016/0006-291x(89)91372-7. [DOI] [PubMed] [Google Scholar]
  17. Thiemermann C., Vane J. Inhibition of nitric oxide synthesis reduces the hypotension induced by bacterial lipopolysaccharides in the rat in vivo. Eur J Pharmacol. 1990 Jul 17;182(3):591–595. doi: 10.1016/0014-2999(90)90062-b. [DOI] [PubMed] [Google Scholar]
  18. Türker R. K., Demirel E., Ercan Z. S. Iloprost preserves kidney function against anoxia. Prostaglandins Leukot Essent Fatty Acids. 1988 Jan;31(1):45–52. doi: 10.1016/0952-3278(88)90164-0. [DOI] [PubMed] [Google Scholar]

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