A 3D human adipose tissue model within a microfluidic device.
A 3D human adipose tissue model within a microfluidic device.
复制标题
DOI:
10.1039/d0lc00981d
复制
发表时间:
2021-01-21
期刊:
影响因子:
6.1
通讯作者:
Brey EM
中科院分区:
文献类型:
--
作者:
Yang F;Carmona A;Stojkova K;Garcia Huitron EI;Goddi A;Bhushan A;Cohen RN;Brey EM
An accurate in vitro model of human adipose tissue could assist in the study of adipocyte function and allow for better tools for screening new therapeutic compounds. Cell culture models on two-dimensional surfaces fall short of mimicking the three-dimensional in vivo adipose environment, while three-dimensional culture models are often unable to support long-term cell culture due, in part, to insufficient mass transport. Microfluidic systems have been explored for adipose tissue models. However, current systems have primarily focused on 2D cultured adipocytes. In this work, a 3D human adipose microtissue was engineered within a microfluidic system. Human adipose-derived stem cells (ADSCs) were used as the cell source for generating differentiated adipocytes. The ADSCs differentiated within the microfluidic system formed a dense lipid-loaded mass with the expression of adipose tissue genetic markers. Engineered adipose tissue showed a decreased adiponectin secretion and increased free fatty acid secretion with increasing shear stress. Adipogenesis markers were downregulated with increasing shear stress. Overall, this microfluidic system enables the on-chip differentiation and development of a functional 3D human adipose microtissue supported by the interstitial flow. This system could potentially serve as a platform for in vitro drug testing for adipose tissue-related diseases. This work presents a microfluidic system for the engineering and analysis of 3D human adipose tissue under controlled flow.
登录
查看更多内容
DOI:
10.1530/joe-13-0339
发表时间:
2014-02
期刊:
The Journal of endocrinology
影响因子:
--
作者:
Cao H
通讯作者:
Cao H
DOI:
10.1039/c4an01725k
发表时间:
2015-02-21
期刊:
The Analyst
影响因子:
--
作者:
Godwin LA;Brooks JC;Hoepfner LD;Wanders D;Judd RL;Easley CJ
通讯作者:
Easley CJ
影响因子:
3
作者:
Gerlach, Joerg C.;Lin, Yen-Chih;Marra, Kacey G.
通讯作者:
Marra, Kacey G.
影响因子:
5.6
作者:
Jung UJ;Choi MS
通讯作者:
Choi MS
影响因子:
6.1
作者:
Hsu YH;Moya ML;Hughes CC;George SC;Lee AP
通讯作者:
Lee AP