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离体大鼠气管灌流液中的糜蛋白酶活性:与黏膜及结缔组织肥大细胞分泌的相关性

Chymotryptic activity in perfusates of isolated rat trachea: correlation with mucosal and connective tissue mast cell secretion.

作者信息

Tam E K, Aufderheide J, Hua X Y

机构信息

Department of Medicine, University of California.

出版信息

Am J Respir Cell Mol Biol. 1994 Sep;11(3):321-8. doi: 10.1165/ajrcmb.11.3.7522016.

Abstract

Serine proteinases participate in many inflammatory events in the airway. We therefore screened perfusates of isolated rat tracheas for tryptic, elastolytic, and chymotryptic serine proteinases. Only chymotryptic activity, indicated by hydrolysis of the synthetic substrate N-succinylalanylalanylprolylphenylalanyl p-nitroaniline (AAPF), was consistently detected in these perfusates. Basal levels of chymotryptic activity were not increased significantly by electrical field stimulation (EFS) (mean change +/- SEM: -0.05 +/- 0.05 m o.d. units, n = 4) or by 10(-7) M substance P (SP) (+0.04 +/- 0.02 m o.d. units, n = 14). However, the mean change after the stimuli were jointly administered (0.17 +/- 0.06 m o.d. units, n = 12) was significantly greater than control or after EFS (P = 0.01, one-way ANOVA). The SP + EFS-induced chymotryptic activity was inhibited by PMSF, soybean trypsin inhibitor, and chymostatin and was associated with an increase in histamine concentration and immunoreactivity to rat mast cell proteases (RMCP), indicating that the activity is due to mast cell degranulation. However, the activity was not significantly decreased by pretreating rats with systemic compound 48/80. SP + EFS-induced chymotryptic activity peaked rapidly and was associated with modest histamine release and an immediate peak in immunoreactivity to RMCP II, a marker of mucosal mast cells. Immunoreactivity to RMCP I, a marker of connective tissue mast cells, also increased after SP + EFS, but this immunoreactivity was either delayed or more sustained and did not coincide with the peak of chymotryptic activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

丝氨酸蛋白酶参与气道中的许多炎症事件。因此,我们对分离的大鼠气管灌流液进行筛选,以寻找胰蛋白酶、弹性蛋白酶和糜蛋白酶样丝氨酸蛋白酶。在这些灌流液中,仅持续检测到由合成底物N-琥珀酰丙氨酰丙氨酰脯氨酰苯丙氨酰对硝基苯胺(AAPF)水解所指示的糜蛋白酶活性。电场刺激(EFS)(平均变化±标准误:-0.05±0.05毫光密度单位,n = 4)或10⁻⁷ M P物质(SP)(+0.04±0.02毫光密度单位,n = 14)均未使基础糜蛋白酶活性显著增加。然而,联合给予刺激后的平均变化(0.17±0.06毫光密度单位,n = 12)显著大于对照组或EFS后(P = 0.01,单因素方差分析)。SP + EFS诱导的糜蛋白酶活性受到苯甲基磺酰氟(PMSF)、大豆胰蛋白酶抑制剂和抑糜酶素的抑制,并且与组胺浓度增加以及对大鼠肥大细胞蛋白酶(RMCP)的免疫反应性增加相关,表明该活性是由于肥大细胞脱颗粒所致。然而,用全身性化合物48/80预处理大鼠并未使该活性显著降低。SP + EFS诱导的糜蛋白酶活性迅速达到峰值,并与适度的组胺释放以及对RMCP II(黏膜肥大细胞的标志物)的免疫反应性立即达到峰值相关。对结缔组织肥大细胞的标志物RMCP I的免疫反应性在SP + EFS后也增加,但这种免疫反应性要么延迟出现,要么持续时间更长,且与糜蛋白酶活性的峰值不一致。(摘要截短于250字)

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