Dynamic single cell culture array

微图形化 微流控 细胞培养 细胞 单细胞分析 生物物理学 基质(水族馆) 赫拉 俘获 人口 材料科学 多电极阵列 化学 纳米技术 细胞生物学 生物 生物化学 电极 微电极 社会学 物理化学 人口学 遗传学 生态学
作者
Dino Di Carlo,Liz Y. Wu,Luke P. Lee
出处
期刊:Lab on a Chip [Royal Society of Chemistry]
卷期号:6 (11): 1445-1445 被引量:706
标识
DOI:10.1039/b605937f
摘要

It is important to quantify the distribution of behavior amongst a population of individual cells to reach a more complete quantitative understanding of cellular processes. Improved high-throughput analysis of single cell behavior requires uniform conditions for individual cells with controllable cell–cell interactions, including diffusible and contact elements. Uniform cell arrays for static culture of adherent cells have previously been constructed using protein micropatterning techniques but lack the ability to control diffusible secretions. Here we present a microfluidic-based dynamic single cell culture array that allows both arrayed culture of individual adherent cells and dynamic control of fluid perfusion with uniform environments for individual cells. In our device no surface modification is required and cell loading is done in less than 30 seconds. The device consists of arrays of physical U-shaped hydrodynamic trapping structures with geometries that are biased to trap only single cells. HeLa cells were shown to adhere at a similar rate in the trapping array as on a control glass substrate. Additionally, rates of cell death and division were comparable to the control experiment. Approximately 100 individual isolated cells were observed growing and adhering in a field of view spanning ∼1 mm2 with greater than 85% of cells maintained within the primary trapping site after 24 hours. Also, greater than 90% of cells were adherent and only 5% had undergone apoptosis after 24 hours of perfusion culture within the trapping array. We anticipate uses in single cell analysis of drug toxicity with physiologically relevant perfused dosages as well as investigation of cell signaling pathways and systems biology.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
帅气小医仙完成签到 ,获得积分20
3秒前
思源应助穆亦擎采纳,获得10
4秒前
daidai完成签到,获得积分10
6秒前
笔墨留香完成签到,获得积分10
8秒前
9秒前
9秒前
Jacqueline完成签到,获得积分10
10秒前
刻苦小丸子完成签到,获得积分10
15秒前
丘比特应助Yuanyuan采纳,获得10
15秒前
华仔应助天天采纳,获得10
16秒前
Lucas应助天天采纳,获得10
16秒前
MING应助科研通管家采纳,获得10
20秒前
慕青应助科研通管家采纳,获得10
21秒前
英俊的铭应助科研通管家采纳,获得10
21秒前
领导范儿应助科研通管家采纳,获得10
21秒前
科研通AI6应助科研通管家采纳,获得10
21秒前
大个应助科研通管家采纳,获得10
21秒前
上官若男应助科研通管家采纳,获得10
21秒前
21秒前
21秒前
烟花应助科研通管家采纳,获得10
21秒前
Wonderland完成签到,获得积分10
21秒前
万寿宫人发布了新的文献求助30
22秒前
嘻嘻发布了新的文献求助10
22秒前
young_lifestyle完成签到,获得积分10
25秒前
酷波er应助UGO采纳,获得10
27秒前
大个应助Kimo采纳,获得10
28秒前
留白完成签到,获得积分10
29秒前
清风发布了新的文献求助10
31秒前
张贵虎发布了新的文献求助10
32秒前
32秒前
墨暮尘尘完成签到,获得积分10
32秒前
Dream发布了新的文献求助10
34秒前
lxl98完成签到 ,获得积分10
34秒前
jiejie完成签到,获得积分10
38秒前
科研通AI2S应助苗浩阳采纳,获得10
39秒前
SciGPT应助jing采纳,获得10
39秒前
奶皮七七发布了新的文献求助10
40秒前
pw关闭了pw文献求助
41秒前
ly1完成签到,获得积分10
45秒前
高分求助中
(应助此贴封号)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Voyage au bout de la révolution: de Pékin à Sochaux 700
First Farmers: The Origins of Agricultural Societies, 2nd Edition 500
Simulation of High-NA EUV Lithography 400
Assessment of adverse effects of Alzheimer's disease medications: Analysis of notifications to Regional Pharmacovigilance Centers in Northwest France 400
The Rise & Fall of Classical Legal Thought 260
Tonal intuitions in "Tristan und Isolde" / by Brian Hyer 200
热门求助领域 (近24小时)
化学 材料科学 医学 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 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4333317
求助须知:如何正确求助?哪些是违规求助? 3845079
关于积分的说明 12010711
捐赠科研通 3485650
什么是DOI,文献DOI怎么找? 1913339
邀请新用户注册赠送积分活动 956497
科研通“疑难数据库(出版商)”最低求助积分说明 857259