1988
DOI: 10.1016/0192-0561(88)90310-4
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CSFs regulate basophil function

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Cited by 17 publications
(31 citation statements)
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“…We also examined the effect of rhIL-2, rhIL-3, and rhGM-CSF on IgE-mediated histamine release from normal donors' blood basophils. Our results show that basophils are activated by rhIL-3 and rhGM-CSF (but not rhIL-2) for increased histamine releasability, which confirms the data obtained by Hirai et al (13). The exact mechanism for this increased response of normal blood basophils to anti-IgE antibodies caused by rhIL-3 and rhGM-CSF remains unknown.…”
supporting
confidence: 81%
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“…We also examined the effect of rhIL-2, rhIL-3, and rhGM-CSF on IgE-mediated histamine release from normal donors' blood basophils. Our results show that basophils are activated by rhIL-3 and rhGM-CSF (but not rhIL-2) for increased histamine releasability, which confirms the data obtained by Hirai et al (13). The exact mechanism for this increased response of normal blood basophils to anti-IgE antibodies caused by rhIL-3 and rhGM-CSF remains unknown.…”
supporting
confidence: 81%
“…Whereas Haak-Frendscho et al (12) described histamine release from blood basophils in direct response to recombinant human IL-3 (rhIL-3) as well as recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF), no direct histamine-releasing activity of these cytokines was found in our own experiments (14). More recently, Hirai et al (13) reported that the histamine release from normal blood basophils induced by various stimuli such as anti-IgE antibodies could be enhanced by preincubation of basophils with rhIL-3 or rhGM-CSF. However, the mechanisms by which rhIL-3 and rhGM-CSF stimulate human blood basophils remain unclear.…”
mentioning
confidence: 99%
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“…[1][2][3][4][5][6] Up to now, many publications in the open literature have been found in synthesis of production of pyromellitic dianhydride (PMDA), and the classical method for such a synthesis constitutes the liquid-phase oxidation of 1,2,4,5-tetraalkyl benzene catalyzed by cobalt, manganese, bromine, nitric acid or dichromic acid in the presence of 100-450 psig, and then dehydrating the obtained pyromellitic acid into pyromellitic dianhydride. [7][8][9][10] However, this procedure is invariably associated with certain limitations such as high cost, long reaction time, environmental hazards, special apparatus and drastic reaction conditions. The catalytic vapor-phase oxidation of 1,2,4,5-tetraalkyl benzene under oxyen pressure using a certain catalyst (e.g.…”
Section: Introductionmentioning
confidence: 99%