Hybrid Biomimetic Interfaces Integrating Supported Lipid Bilayers with Decellularized Extracellular Matrix Components

被引:7
|
作者
Vafaei, Setareh [1 ,2 ]
Tabaei, Seyed R. [1 ,2 ]
Guneta, Vipra [1 ]
Choong, Cleo [1 ,3 ]
Cho, Nam-Joon [1 ,2 ,4 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Ctr Biomimet Sensor Sci, 50 Nanyang Dr, Singapore 637553, Singapore
[3] KK Womens & Childrens Hosp, KK Res Ctr, 100 Bukit Timah Rd, Singapore 229899, Singapore
[4] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
基金
新加坡国家研究基金会;
关键词
CELL-ADHESION; PHOSPHOLIPID-BILAYERS; SIGNAL-TRANSDUCTION; STEM-CELLS; QCM-D; MEMBRANES; PROTEIN; ADSORPTION; SCAFFOLDS; PEPTIDE;
D O I
10.1021/acs.langmuir.7b03265
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper describes the functionalization of solid supported phospholipid bilayer with decellularized extracellular matrix (dECM) components, toward the development of biomimetic platforms that more closely mimic the cell surface environment. The dECM was obtained through a combination of chemical and enzymatic treatments of mouse adipose tissue that contains collagen, fibronectin, and glycosaminoglycans (GAGs). Using amine coupling chemistry, the dECM components were attached covalently to the surface of a supported lipid bilayer containing phospholipids with reactive carboxylic acid headgroups. The bilayer formation and the kinetics of subsequent dECM conjugation were monitored by quartz crystal microbalance with dissipation (QCM-D). Fluorescence recovery after photobleaching (FRAP) confirmed the fluidity of the membrane after functionalization with dECM. The resulting hybrid biomimetic interface supports the attachment and survival of the human hepatocyte Huh 7.5 and maintains the representative hepatocellular function. Importantly, the platform is suitable for monitoring the lateral organization and clustering of cell-binding ligands and growth factor receptors in the presence of the rich biochemical profile of tissue-derived ECM components.
引用
收藏
页码:3507 / 3516
页数:10
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