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胰蛋白酶可诱导人白血病肥大细胞系分泌肿瘤坏死因子-α。

Trypsin induces tumour necrosis factor-alpha secretion from a human leukemic mast cell line.

作者信息

Kang Ok-Hwa, Jeong Hyun-Ja, Kim Dae-Ki, Choi Suck-Chei, Kim Tae-Hyun, Nah Yong-Ho, Kim Hyung-Min, Lee Young-Mi

机构信息

Department of Oriental Pharmacy, College of Pharmacy, Wonkwang University, Iksan, Chonbuk, 570-749, South Korea.

出版信息

Cell Biochem Funct. 2003 Jun;21(2):161-7. doi: 10.1002/cbf.1014.

Abstract

Trypsin activating both proteinase-activated receptor (PAR) 2 and PAR4 plays an important role in inflammation. We have investigated the potential of trypsin to induce TNF-alpha secretion from the human leukemic mast cell line (HMC-1). HMC-1 cells co-express both PAR2 and PAR4, and their agonist trypsin signals to HMC-1 cells. Trypsin (100 nm), SLIGKV-NH(2) (100 microm, corresponding to the PAR2 tethered ligand), or GYPGQV-NH(2) (100 microm, corresponding to the PAR4 tethered ligand) induced tumour necrosis factor (TNF)-alpha secretion from HMC-1 cells. TNF-alpha secretion by trypsin was significantly blocked by pretreatment with 50 microm PD098059, MEK-1 inhibitor. Furthermore, trypsin stimulated the activation of extracellular signal-regulated kinase (ERK) in HMC-1 cells without any detectable activation of c-Jun N-terminal kinase (JNK) and p38 MAP kinase homologue. These results show that trypsin may induce TNF-alpha secretion following activation of ERK via both PAR2 and PAR4 on HMC-1 cells.

摘要

胰蛋白酶可激活蛋白酶激活受体(PAR)2和PAR4,在炎症反应中发挥重要作用。我们研究了胰蛋白酶诱导人白血病肥大细胞系(HMC-1)分泌肿瘤坏死因子-α(TNF-α)的可能性。HMC-1细胞同时表达PAR2和PAR4,其激动剂胰蛋白酶可向HMC-1细胞发出信号。胰蛋白酶(100 nM)、SLIGKV-NH₂(100 μM,对应PAR2拴系配体)或GYPGQV-NH₂(100 μM,对应PAR4拴系配体)均可诱导HMC-1细胞分泌肿瘤坏死因子(TNF)-α。用50 μM的MEK-1抑制剂PD098059预处理可显著阻断胰蛋白酶诱导的TNF-α分泌。此外,胰蛋白酶可刺激HMC-1细胞中细胞外信号调节激酶(ERK)的激活,而未检测到c-Jun氨基末端激酶(JNK)和p38丝裂原活化蛋白激酶同源物的激活。这些结果表明,胰蛋白酶可能通过激活HMC-1细胞上的PAR2和PAR4,进而激活ERK,从而诱导TNF-α分泌。

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