Macrophage polarization in THP-1 cell line and primary monocytes: A systematic review

THP1细胞系 单核细胞白血病 生物 巨噬细胞极化 单核细胞 免疫系统 细胞培养 巨噬细胞 体外 免疫学 计算生物学 细胞生物学 生物化学 遗传学
作者
Zahidah Nasuha Mohd Yasin,Fatin Najiah Mohd Idrus,Chee Hock Hoe,Get Bee Yvonne-Τee
出处
期刊:Differentiation [Elsevier]
卷期号:128: 67-82 被引量:36
标识
DOI:10.1016/j.diff.2022.10.001
摘要

Macrophages derived from human monocytic leukemia THP-1 cell line are often used as the alternative of human primary macrophage. However, the polarization method of THP-1 to macrophages varies between different laboratories, which may unknowingly affect the relevance of research output across research groups. In this regard, a systematic search was developed in Pubmed, BioOne, Scopus, and Science Direct to identify articles focusing on THP-1 polarization into M1 and M2 macrophages. All selected articles were read and discussed by two independent reviewers. The selection process was based on selected keywords on the title, abstract and full-text level. A total of 85 articles were selected and categorized based on the field of studies, method of THP-1 differentiation, and markers or genes expressed upon differentiation. THP-1 derived macrophages were mainly used together with primary monocyte-derived macrophages in cellular inflammation studies, while it was commonly employed alone in cancer research. THP-1 derived macrophages are also of paramount importance in biomaterials studies to prevent unfavorable immune responses in-vivo. We explored various methods of THP-1 differentiation and suggested several common genes encountered to characterize M1 and M2 macrophages differentiated from THP-1. The systematic review highlights the relevance of using THP-1 derived macrophage as a useful alternative to primary macrophage. Although it is not possible to derive a standard method of THP-1 polarization into M1 and M2 macrophages from this review, it may lead researchers to obtain reproducible polarization protocol based on commonly used stimulants and markers of differentiation.
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
flee完成签到,获得积分10
1秒前
1秒前
娇娇大王完成签到,获得积分10
5秒前
6秒前
雄哥关注了科研通微信公众号
10秒前
21完成签到 ,获得积分10
11秒前
谢健完成签到 ,获得积分10
11秒前
从容芮应助flee采纳,获得30
11秒前
外向梨愁完成签到 ,获得积分20
16秒前
慕青应助科研通管家采纳,获得10
23秒前
Orange应助科研通管家采纳,获得10
23秒前
科目三应助科研通管家采纳,获得10
23秒前
天天快乐应助科研通管家采纳,获得10
23秒前
搜集达人应助科研通管家采纳,获得10
23秒前
隐形曼青应助科研通管家采纳,获得10
23秒前
CipherSage应助科研通管家采纳,获得10
23秒前
丘比特应助科研通管家采纳,获得10
23秒前
23秒前
Dusk大寺柯完成签到 ,获得积分10
34秒前
鳗鱼三毒发布了新的文献求助10
35秒前
TOM龙完成签到,获得积分10
37秒前
星海完成签到,获得积分10
38秒前
Nicole完成签到,获得积分10
38秒前
xiaoqianqian174完成签到,获得积分10
41秒前
48秒前
lxyonline发布了新的文献求助10
53秒前
年轻的凝云完成签到 ,获得积分10
54秒前
Agoni完成签到 ,获得积分20
57秒前
不辩完成签到 ,获得积分10
1分钟前
SSS关注了科研通微信公众号
1分钟前
一样不一样完成签到,获得积分10
1分钟前
1分钟前
小t要读top博完成签到,获得积分10
1分钟前
1分钟前
笨笨的又蓝完成签到,获得积分10
1分钟前
1分钟前
1DDDDD完成签到,获得积分10
1分钟前
Breath发布了新的文献求助30
1分钟前
KneeYu应助weiyashu采纳,获得10
1分钟前
真三发布了新的文献求助10
1分钟前
高分求助中
LNG地下式貯槽指針(JGA Guideline-107)(LNG underground storage tank guidelines) 1000
Second Language Writing (2nd Edition) by Ken Hyland, 2019 1000
Generalized Linear Mixed Models 第二版 1000
rhetoric, logic and argumentation: a guide to student writers 1000
QMS18Ed2 | process management. 2nd ed 1000
Asymptotically optimum binary codes with correction for losses of one or two adjacent bits 800
Operative Techniques in Pediatric Orthopaedic Surgery 510
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2923471
求助须知:如何正确求助?哪些是违规求助? 2568831
关于积分的说明 6941912
捐赠科研通 2223517
什么是DOI,文献DOI怎么找? 1181936
版权声明 588950
科研通“疑难数据库(出版商)”最低求助积分说明 578406