Hirasawa N, Ohuchi K
Laboratory of Pathophysiological Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba Aramaki, Aoba-ku, Sendai, Miyagi 980-8578, Japan.
Nihon Yakurigaku Zasshi. 2001 Jul;118(1):23-8. doi: 10.1254/fpj.118.23.
Stimulating cells of the mouse macrophage-like cell line RAW 264.7 with the Ca(2+)-ATPase inhibitor thapsigargin increased histamine production. Thapsigargin increased the levels of histidine decarboxylase (HDC) mRNA at 4 h and the expression of 74-kDa HDC protein at 8 h. PD98059, a specific inhibitor of MEK-1 which phosphorylates p44/p42 MAP kinase, strongly suppressed the thapsigargin-induced histamine production, the increase in HDC mRNA level and 74-kDa HDC protein expression. In contrast, SB203580, an inhibitor of p38 MAP kinase, showed only a partial inhibition of histamine production. TPA and LPS also induced histamine production in RAW 264.7 cells, and the histamine production induced by TPA or LPS was also inhibited by PD98059, but the effect of SB203580 was partial. The synthetic glucocorticoid dexamethasone inhibited thapsigargin-induced histamine production, 74-kDa HDC protein expression and the activation of p44/p42 MAP kinases. In conclusion, the increase in histamine production in macrophages stimulated with inflammatory stimulants is due to the increased expression of 74-kDa HDC, which is positively regulated by activated p44/p42 MAP kinases. Dexamethasone inhibits thapsigargin-induced HDC protein expression and histamine production by inhibiting the MAP kinase activation.
用钙离子 - ATP酶抑制剂毒胡萝卜素刺激小鼠巨噬细胞样细胞系RAW 264.7的细胞,可增加组胺的产生。毒胡萝卜素在4小时时增加了组氨酸脱羧酶(HDC)mRNA的水平,并在8小时时增加了74 kDa HDC蛋白的表达。PD98059是一种磷酸化p44/p42丝裂原活化蛋白激酶(MAP激酶)的MEK - 1的特异性抑制剂,它强烈抑制毒胡萝卜素诱导的组胺产生、HDC mRNA水平的增加以及74 kDa HDC蛋白的表达。相比之下,p38 MAP激酶抑制剂SB203580仅部分抑制组胺的产生。佛波酯(TPA)和脂多糖(LPS)也诱导RAW 264.7细胞产生组胺,并且TPA或LPS诱导的组胺产生也被PD98059抑制,但SB203580的作用是部分性的。合成糖皮质激素地塞米松抑制毒胡萝卜素诱导的组胺产生、74 kDa HDC蛋白表达以及p44/p42 MAP激酶的激活。总之,炎症刺激物刺激巨噬细胞时组胺产生的增加是由于74 kDa HDC表达的增加,而74 kDa HDC受到活化的p44/p42 MAP激酶的正向调节。地塞米松通过抑制MAP激酶的激活来抑制毒胡萝卜素诱导的HDC蛋白表达和组胺产生。