Liquid crystalline matrix-induced viscoelastic mechanical stimulation modulates activation and phenotypes of macrophage

巨噬细胞极化 材料科学 粘弹性 巨噬细胞 细胞生物学 生物物理学 体外 化学 生物 复合材料 生物化学
作者
Lichu Liu,Tao Huang,Zheng Xie,Zhangyao Ye,Jiaqing Zhang,Honghong Liao,Shenyu Yang,Kuangyang Yang,Mei Tu
出处
期刊:Journal of Biomaterials Applications [SAGE]
卷期号:37 (9): 1568-1581
标识
DOI:10.1177/08853282221136580
摘要

Accumulating evidence indicates that the mechanical microenvironment exerts profound influences on inflammation and immune modulation, which are likely to be key factors in successful tissue regeneration. The elastic modulus (Em) of the matrix may be a useful adjustable property to control macrophage activation and the overall inflammatory response. This study constituted a series of Em-tunable liquid crystalline cell model (HpCEs) resembling the viscoelastic characteristic of ECM and explored how mechanical microenvironment induced by liquid crystalline soft matter matrix affected macrophage activation and phenotypes. We have shown that HpCEs prepared in this work exhibited typical cholesteric liquid crystal phase and distinct viscoelastic rheological characteristics. All liquid crystalline HpCE matrices facilitated macrophages growth and maintained cell activity. Macrophages in lower-Em HpCE matrices were more likely to polarize toward the pro-inflammatory M1 phenotype. Conversely, the higher-Em HpCEs induced macrophages into an elongated shape and upregulated M2-related markers. Furthermore, the higher-Em HpCEs (HpCE-O1, HpCE-H2, HpCE-H1) could coax sequential polarization states of RAW264.7 from a classically activated “M1” state toward alternatively activated “M2” state in middle and later stage of cell culture (within 3–7 days in this work), suggesting that the HpCE-based strategies could manipulate the local immune microenvironment and promote the dominance of the pro-inflammatory signals in early stages, while M2 macrophages in later stages. The liquid crystalline soft mode fabricated in this work maybe offer a new design guideline for in vitro cell models and applications.
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
刚刚
慕青应助科研通管家采纳,获得20
刚刚
SciGPT应助科研通管家采纳,获得10
刚刚
打打应助科研通管家采纳,获得10
刚刚
刚刚
1秒前
dongsheng应助科研通管家采纳,获得10
1秒前
我是老大应助科研通管家采纳,获得10
1秒前
1秒前
1秒前
云云发布了新的文献求助10
1秒前
手机应助wu采纳,获得20
1秒前
调研昵称发布了新的文献求助10
2秒前
Jasper应助司空蓝采纳,获得10
3秒前
白玫瑰完成签到,获得积分10
4秒前
小n发布了新的文献求助10
5秒前
bkagyin应助一一采纳,获得10
5秒前
科研通AI2S应助高贵芷波采纳,获得10
8秒前
pluto应助Rui采纳,获得10
11秒前
李健的小迷弟应助Rui采纳,获得10
11秒前
香蕉子骞完成签到 ,获得积分10
12秒前
共享精神应助Max采纳,获得10
14秒前
15秒前
漫漫楚威风完成签到,获得积分10
16秒前
不安青牛应助潜放采纳,获得10
16秒前
不安青牛应助乐观的冰珍采纳,获得10
18秒前
Orange应助白樱恋曲采纳,获得10
18秒前
汉堡包应助风中冷风采纳,获得10
18秒前
LSL丶完成签到,获得积分10
18秒前
CC给CC的求助进行了留言
19秒前
缥缈不惜发布了新的文献求助10
20秒前
20秒前
QinQin发布了新的文献求助30
22秒前
BAMM完成签到,获得积分20
22秒前
一一发布了新的文献求助10
24秒前
科研通AI2S应助云云采纳,获得10
26秒前
27秒前
要减肥的书萱关注了科研通微信公众号
27秒前
27秒前
顾城浪子完成签到,获得积分10
29秒前
高分求助中
Mantiden: Faszinierende Lauerjäger Faszinierende Lauerjäger Heßler, Claudia, Rud 1000
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 1000
Natural History of Mantodea 螳螂的自然史 1000
A Photographic Guide to Mantis of China 常见螳螂野外识别手册 800
Autoregulatory progressive resistance exercise: linear versus a velocity-based flexible model 500
Spatial Political Economy: Uneven Development and the Production of Nature in Chile 400
Research on managing groups and teams 300
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 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3329457
求助须知:如何正确求助?哪些是违规求助? 2959146
关于积分的说明 8594359
捐赠科研通 2637590
什么是DOI,文献DOI怎么找? 1443651
科研通“疑难数据库(出版商)”最低求助积分说明 668775
邀请新用户注册赠送积分活动 656220