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:40
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
乐乐应助十三儿采纳,获得10
刚刚
1秒前
2秒前
2秒前
Romitavia完成签到,获得积分20
2秒前
医路有你发布了新的文献求助10
2秒前
2秒前
3秒前
3秒前
realeagle发布了新的文献求助10
3秒前
sss关闭了sss文献求助
3秒前
爱听歌的艳完成签到,获得积分20
4秒前
5秒前
wink完成签到,获得积分10
5秒前
Mars1998发布了新的文献求助10
6秒前
得到太阳发布了新的文献求助10
7秒前
桐桐应助辛勤的大雁采纳,获得10
7秒前
7秒前
尹尹尹发布了新的文献求助10
8秒前
8秒前
YY发布了新的文献求助10
9秒前
wink发布了新的文献求助10
9秒前
六月初八夜完成签到,获得积分10
11秒前
ira发布了新的文献求助10
12秒前
12秒前
12秒前
Lynx完成签到,获得积分10
12秒前
咩咩完成签到,获得积分10
13秒前
田様应助个性的南珍采纳,获得10
14秒前
why完成签到,获得积分10
15秒前
mile发布了新的文献求助10
15秒前
16秒前
从容芮应助Mars1998采纳,获得10
16秒前
Lynx发布了新的文献求助10
19秒前
23秒前
chai完成签到,获得积分10
25秒前
26秒前
科目三应助科研通管家采纳,获得10
27秒前
华仔应助科研通管家采纳,获得10
27秒前
月野兔完成签到,获得积分10
27秒前
高分求助中
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
Rechtsphilosophie 1000
Bayesian Models of Cognition:Reverse Engineering the Mind 888
Le dégorgement réflexe des Acridiens 800
Defense against predation 800
Very-high-order BVD Schemes Using β-variable THINC Method 568
热门求助领域 (近24小时)
化学 医学 生物 材料科学 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 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3136629
求助须知:如何正确求助?哪些是违规求助? 2787671
关于积分的说明 7782749
捐赠科研通 2443752
什么是DOI,文献DOI怎么找? 1299386
科研通“疑难数据库(出版商)”最低求助积分说明 625440
版权声明 600954