The G Protein–Coupled Receptor GPR56 Is an Inhibitory Checkpoint for NK Cell Migration

细胞生物学 生物 细胞迁移 小干扰RNA 细胞 细胞培养 转染 遗传学
作者
Daniel Palacios,Rakesh Kumar Majhi,Edina K. Szabo,Dennis Clement,Mieszko Lachota,Herman Netskar,Leena Penna,Silje Zandstra Krokeide,Marianna Vincenti,Lise Kveberg,Karl‐Johan Malmberg
出处
期刊:Journal of Immunology [American Association of Immunologists]
卷期号:213 (9): 1349-1357 被引量:7
标识
DOI:10.4049/jimmunol.2400228
摘要

G protein-coupled receptors (GPCRs) represent the largest family of surface receptors and are responsible for key physiological functions, including cell growth, neurotransmission, hormone release, and cell migration. The GPCR 56 (GPR56), encoded by ADGRG1, is an adhesion GPCR found on diverse cell types, including neural progenitor cells, melanoma cells, and lymphocytes, such as effector memory T cells, γδ T cells, and NK cells. Using RNA-sequencing and high-resolution flow cytometry, we found that GPR56 mRNA and protein expression increased with NK cell differentiation, reaching its peak in adaptive NK cells. Small interfering RNA silencing of GPR56 led to increased spontaneous and chemokine-induced migration, suggesting that GPR56 functions as an upstream checkpoint for migration of highly differentiated NK cells. Increased NK cell migration could also be induced by agonistic stimulation of GPR56 leading to rapid internalization and deactivation of the receptor. Mechanistically, GPR56 ligation and downregulation were associated with transcriptional coactivator with PDZ-binding motif translocation to the nucleus and increased actin polymerization. Together, these data provide insights into the role of GPR56 in the migratory behavior of human NK cell subsets and may open possibilities to improve NK cell infiltration into cancer tissues by releasing a migratory checkpoint.
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
Orange应助平淡新晴采纳,获得10
刚刚
林兰特发布了新的文献求助20
刚刚
彭佳丽发布了新的文献求助10
刚刚
2秒前
2秒前
杨武天一完成签到,获得积分10
3秒前
orixero应助椰灵采纳,获得10
3秒前
dadadad完成签到,获得积分10
3秒前
3秒前
wuweizhizhi发布了新的文献求助10
4秒前
大方道消完成签到,获得积分10
4秒前
5秒前
bkagyin应助sanshu采纳,获得10
6秒前
whisper完成签到 ,获得积分10
7秒前
机智毛豆发布了新的文献求助10
7秒前
7秒前
英俊的铭应助yyyhhh采纳,获得30
7秒前
JamesPei应助幸福台灯采纳,获得10
7秒前
隐形曼青应助vffg采纳,获得10
8秒前
蓝02333发布了新的文献求助10
8秒前
8秒前
8秒前
8秒前
平淡新晴发布了新的文献求助10
9秒前
天天快乐应助松林采纳,获得10
10秒前
彭于晏应助右右采纳,获得10
11秒前
大意的葶完成签到,获得积分10
11秒前
12秒前
Lucas应助大男采纳,获得10
12秒前
zLin完成签到,获得积分10
12秒前
shubido完成签到,获得积分10
13秒前
汪大灰发布了新的文献求助30
13秒前
DanL发布了新的文献求助10
14秒前
14秒前
Surpass发布了新的文献求助10
14秒前
学废了完成签到 ,获得积分10
15秒前
ky完成签到,获得积分10
16秒前
一一发布了新的文献求助10
16秒前
cxr完成签到,获得积分10
17秒前
18秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7296568
求助须知:如何正确求助?哪些是违规求助? 8914913
关于积分的说明 18877119
捐赠科研通 6962654
什么是DOI,文献DOI怎么找? 3210451
关于科研通互助平台的介绍 2379695
邀请新用户注册赠送积分活动 2186822