Human basiphilic leukocytes and mast cells are markedly pro-inflammatory cells that release a number of chemical mediators, including histamine and SRS-A, after immunologic stimulation involving cross-linking of cell surface-bound IgE molecules. Although numerous studies have been performed using human lunlg parenchymal fragments containing a mixture of cell types, and rodent cells, detailed biochemical and immunologic studies have not been performed using purified human mast cells. Recently, we have developed a techique for the purification of human lung mast cells to purities of greater than 95% by enzymatic dispersion, centrifugation by countercurrent elutriation, and immunoaffinity chromatography. Using purified preparations of these cels, we plan to quanttate mediators of inflmammation produced by these cells including SRS-A, prostaglandings, and lysosomal hydrolases; quantitate the lipoxygenase products of arachidonic acid produced by these cells and determine the role of these products in histamine release; explore biochemical mechanisms involved in mediator release from these cells; and explore methods for the pharmacologic control of these pro-inflammatory cells. Such studies promise not only to provide important information concerning the cell biology and biochemistr of human lung mast cells, but also information about pulmonary disease states such as bronchial asthma and chronic inflammatory disorders that are likely due, at least in part, to the inflammatory process and inflammatory mediators.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HL001034-04
Application #
3081653
Study Section
(SRC)
Project Start
1982-07-01
Project End
1986-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Warner, J A; Peters, S P; Lichtenstein, L M et al. (1989) Differential release of mediators from human basophils: differences in arachidonic acid metabolism following activation by unrelated stimuli. J Leukoc Biol 45:558-71
Freed, A N; Peters, S P; Menkes, H A (1987) Airflow-induced bronchoconstriction: role of epithelium and eicosanoid mediators. J Appl Physiol 62:574-81
Peters, S P; Freeland, H S; Kelly, S J et al. (1987) Is leukotriene B4 an important mediator in human IgE-mediated allergic reactions? Am Rev Respir Dis 135:S42-5
Kleeberger, S R; Kolbe, J; Adkinson Jr, N F et al. (1987) Thromboxane contributes to the immediate antigenic response of canine peripheral airways. J Appl Physiol 62:1589-95
Kleeberger, S R; Kolbe, J; Adkinson Jr, N F et al. (1986) Central role of cyclooxygenase in the response of canine peripheral airways to antigen. J Appl Physiol 61:1309-15
Peters, S P; Lichtenstein, L M; Adkinson Jr, N F (1986) Mediator release from human lung under conditions of reduced oxygen tension. J Pharmacol Exp Ther 238:8-13
Peters, S P; Naclerio, R M; Schleimer, R P et al. (1986) The pharmacologic control of mediator release from human basophils and mast cells. Respiration 50 Suppl 2:116-22
Peters, S P; Naclerio, R M; Freeland, H S et al. (1985) Mast cells and mast cell mediators in models of airway disease. Prog Clin Biol Res 199:153-61