A Distinct Regulatory Role of Th17 Cytokines IL-17A and IL-17F in Chemokine Secretion from Lung Microvascular Endothelial Cells

CXCL1型 CXCL5型 趋化因子 CXCL2型 白细胞介素8 白细胞介素17 趋化因子受体 分泌物 细胞因子 免疫学 细胞生物学 化学 生物 内科学 炎症 医学 趋化因子受体
作者
Hitomi Fujie,Kaijun Niu,Michiru Ohba,Yoshihisa Tomioka,Haruki Kitazawa,Kengo Nagashima,Takashi Ohrui,Muneo Numasaki
出处
期刊:Inflammation [Springer Science+Business Media]
卷期号:35 (3): 1119-1131 被引量:49
标识
DOI:10.1007/s10753-011-9419-0
摘要

Th17 cytokines IL-17A and IL-17F play a critical role in the activation and recruitment of neutrophils at airway inflammation mainly through the induction of CXC chemokines in the lungs. Vascular endothelial cells belong to the category of major CXC chemokine-producing cells. However, until now, the precise role of Th17 cytokines in CXC chemokine secretion in lung microvascular endothelial cells (LMVECs) has not been fully elucidated. In this study, we examined the biological effects of Th17 cytokines IL-17A and IL-17F on CXCL1, CXCL5, and CXCL8 release in LMVECs. Both IL-17 receptor A (IL-17RA) and IL-17RC are expressed on the surface of LMVECs. In contrast to IL-17F, IL-17A significantly upregulated CXCL1 mRNA expression and protein release, whereas both IL-17A and IL-17F did not have the ability to induce CXCL5 and CXCL8 secretion in LMVECs. IL-17A and IL-17F displayed positive regulatory effects on IL-1β-induced CXCL1, CXCL5, and CXCL8 secretion. On the other hand, IL-17A enhanced the upregulating effect of TNF-α on CXCL1, CXCL5, and CXCL8 release, whereas IL-17F had a negative regulatory effect on TNF-α-mediated secretion. Th2 cytokines IL-4 and IL-13 showed an inhibitory effect on IL-1β plus IL-17A-induced CXCL1, CXCL5, and CXCL8 secretion, but displayed a positive regulatory effect on TNF-α plus IL-17A-induced secretion. These results provide evidence that Th17 cytokines IL-17A and IL-17F have a distinct regulatory role in CXCL1, CXCL5, and CXCL8 expression in LMVECs stimulated either with IL-1β or with TNF-α. Our findings also suggest that CXC chemokine secretion in LMVECs may be complicatedly regulated by Th17 cytokines, Th2 cytokines, and macrophage-associated cytokines in pathological conditions such as bronchial asthma.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
眼睛大的友易完成签到,获得积分10
刚刚
陪你闯荡发布了新的文献求助10
刚刚
战魂发布了新的文献求助10
1秒前
拉长的采梦完成签到,获得积分10
1秒前
1秒前
可爱的函函应助某强采纳,获得10
1秒前
李健的小迷弟应助sam采纳,获得30
1秒前
缥缈冥发布了新的文献求助10
1秒前
1秒前
LM完成签到,获得积分10
1秒前
小二郎应助JunfDai采纳,获得10
2秒前
2秒前
脑洞疼应助吴祥坤采纳,获得10
2秒前
蔺映秋完成签到,获得积分10
2秒前
Ava应助fengdengjin采纳,获得10
2秒前
2秒前
豆本豆完成签到,获得积分10
3秒前
3秒前
一一发布了新的文献求助10
3秒前
nn发布了新的文献求助10
3秒前
3秒前
高贵电源完成签到 ,获得积分20
3秒前
ii完成签到,获得积分20
3秒前
秀儿发布了新的文献求助10
4秒前
4秒前
ql完成签到 ,获得积分20
4秒前
4秒前
zhuo完成签到,获得积分10
4秒前
无极微光应助dyr采纳,获得20
4秒前
卡萨卡萨完成签到,获得积分10
4秒前
xiaoma完成签到,获得积分10
4秒前
薄饼哥丶发布了新的文献求助10
5秒前
隐形曼青应助勤恳依风采纳,获得10
5秒前
大模型应助顺利的小白菜采纳,获得10
5秒前
猫猫文关注了科研通微信公众号
6秒前
ning发布了新的文献求助10
6秒前
6秒前
科目三应助顺利毕业采纳,获得10
6秒前
DW应助freya采纳,获得10
6秒前
郑慧方发布了新的文献求助10
6秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7762759
求助须知:如何正确求助?哪些是违规求助? 9307387
关于积分的说明 20300169
捐赠科研通 7347359
什么是DOI,文献DOI怎么找? 3313760
关于科研通互助平台的介绍 2463609
邀请新用户注册赠送积分活动 2327902