亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

20 Years an Orphan: Is GPR84 a Plausible Medium-Chain Fatty Acid-Sensing Receptor?

受体 生物 炎症 体内 促炎细胞因子 细胞生物学 受体表达 免疫学 生物化学 遗传学
作者
Vincent B. Luscombe,Daniel Lucy,Carole J. R. Bataille,Angela J. Russell,David R. Greaves
出处
期刊:DNA and Cell Biology [Mary Ann Liebert, Inc.]
卷期号:39 (11): 1926-1937 被引量:33
标识
DOI:10.1089/dna.2020.5846
摘要

GPR84 is an inflammation-induced receptor highly expressed on immune cells, yet its endogenous ligand is still unknown. This makes any interpretation of its physiological activity in vivo difficult. However, experiments with potent synthetic agonists have highlighted what the receptor can do, namely, enhance proinflammatory signaling and macrophage effector functions such as phagocytosis. Developing drugs to block these effects has attracted interest from the scientific community with the aim of decreasing disease activity in inflammatory disorders or enhancing inflammation resolution. In this review, we critically reassess the widely held belief that the major role of GPR84 is that of being a medium-chain fatty acid (MCFA) receptor. While MCFAs have been shown to activate GPR84, it remains to be demonstrated that they are present in relevant tissues at appropriate concentrations. In contrast to four other “full-time” free fatty acid receptor subtypes, GPR84 is not expressed by enteroendocrine cells and has limited expression in the gastrointestinal tract. Across multiple tissues and cell types, the highest expression levels of GPR84 are observed hours after exposure to an inflammatory stimulus. These factors obscure the relationship between ligand and receptor in the human body and do not support the exclusive physiological pairing of MCFAs with GPR84. To maximize the chances of developing efficacious drugs for inflammatory diseases, we must advance our understanding of GPR84 and what it does in vivo.
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
1秒前
4秒前
6秒前
8秒前
8秒前
11秒前
13秒前
16秒前
18秒前
21秒前
24秒前
26秒前
29秒前
29秒前
31秒前
34秒前
36秒前
39秒前
42秒前
44秒前
47秒前
iman完成签到,获得积分10
48秒前
49秒前
52秒前
54秒前
57秒前
水寒风似刀完成签到,获得积分10
59秒前
59秒前
1分钟前
勤劳的唇膏完成签到,获得积分10
1分钟前
忘忧Aquarius完成签到,获得积分0
1分钟前
1分钟前
1分钟前
1分钟前
机灵善斓完成签到,获得积分10
1分钟前
1分钟前
null关闭了YY的文献求助
1分钟前
1分钟前
1分钟前
1分钟前
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
Das Matthäusevangelium: Kapitel 1:1–17 1000
IRTSD: Open-Source Data and Toolset for Electromagnetic Transient Analysis of Disturbances and IBR Control Malfunctions in Transmission Systems 1000
Entre Praga y Madrid : los contactos checoslovaco-españoles (1948-1977) 600
Les Mots du discours 600
A Consideration on Use of Material Grades for Hull Structural Members Based on Fracture Toughness(Second Report) 500
AI Disclosure in Annual Reports: Evolution, Determinants, and Capital Market Participants’ Perceptions 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 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8115277
求助须知:如何正确求助?哪些是违规求助? 9521406
关于积分的说明 21533531
捐赠科研通 7693481
什么是DOI,文献DOI怎么找? 3413534
关于科研通互助平台的介绍 2539837
邀请新用户注册赠送积分活动 2453572