Abstract
Guinea pig lungs were perfused for 15 min with a solution of protease type VII (0.05 mg/ml) and dispersed to yield a suspension of morphologically intact and metabolically active lung cells (over 250 × 106 cells per animal). The viability of these cells assessed with the Trypan blue exclusion technique was more than 80%. Treatment of these mixed cells (1 × 106 cells/ml) with chemicals such as phorbol myristate acetate (1 × 10−9 to 1 × 10−7 M), f-Met-Leu-Phe (5 × 10−6 to 1 x 10−4 M), and the calcium ionophore A23187 (3.1 × 10−7 to 2.5 × 10−6 M), and with autacoids such as bradykinin (1 × 10−5 to 1 × 10−4 M), leukotriene B4 (1 × 10−13 to 1 × 10−7 M), and leukotriene D4 (1 × 10−10 to 1 × 10−7 M) stimulated to a variable degree the release of prostaglandin E2 and thromboxane B2 (measured with a novel enzyme immunoassay). It is suggested that icosanoid release from the lungs is the result of direct chemical or hormonal stimulation of the cells and not a consequence of vascular changes. Studies are in progress to purify lung cell populations and characterize the cells responsible for the release of these icosanoids.
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This work was supported by the Medical Research Council of Canada (MT-7143).
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Robidoux, C., Pelé, J.P., Maclouf, J. et al. Stimulation of release of prostaglandins and thromboxanes from isolated guinea pig lung cells by Bradykinin, f-Met-Leu-Phe, phorbol myristate, ionophore a23187, and leukotrienes. Inflammation 12, 285–295 (1988). https://doi.org/10.1007/BF00915766
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DOI: https://doi.org/10.1007/BF00915766