Cellular behavior in micropatterned hydrogels by bioprinting system depended on the cell types and cellular interaction

被引:51
作者
Hong, Soyoung [1 ,2 ]
Song, Seung-Joon [1 ,2 ]
Lee, Jae Yeon [2 ]
Jang, Hwanseok [1 ,2 ]
Choi, Jaesoon [2 ]
Sun, Kyung [1 ,2 ,4 ]
Park, Yongdoo [1 ,2 ,3 ]
机构
[1] Korea Univ, Dept Biomed Engn, Coll Med, Biomed Sci Brain Korea 21, Seoul 136705, South Korea
[2] Korea Univ, Korea Artificial Organ Ctr, Seoul 136705, South Korea
[3] Korea Univ, Dept Biomed Engn, Coll Med, Seoul 136705, South Korea
[4] Korea Univ, Dept Thorac & Cardiovasc Surg, Coll Med, Seoul 136705, South Korea
基金
新加坡国家研究基金会;
关键词
Bioprinting; Cell aggregation; Hydrogel patterning; Cell migration; Cell-cell interaction; MESENCHYMAL STEM-CELLS; IN-VITRO; GROWTH-FACTOR; BONE-MARROW; MIGRATION; TISSUE; REGENERATION; DYNAMICS; CANCER;
D O I
10.1016/j.jbiosc.2013.02.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The fabrication of patterned microstructures within three-dimensional (3D) matrices is a challenging subject in tissue engineering and regenerative medicine. A 3D, free-moving bioprinting system was developed and hydrogels were patterned by varying the process parameters of z-axis moving velocity and ejection velocity. The patterning of hydrogel based microfibers in a 3D matrigel was achieved with dimensions of 4.5 mm length and widths from 79 to 200 mu m. Hyaluronan-based hydrogels mixed with fibroblasts (L929), mouse endothelial cells (MS1), or human mesenchymal stem cells (hMSCs) were patterned using a 3D moving axis bioprinter and cell behavior was monitored in culture for up to 16 days. L929 and MS1 cells and hMSCs in patterned hydrogel revealed cell-cell interactions and a morphological dependency on cell types. HMSCs formed spheres through cell aggregation, while L929 cells increased in cellular mass without cell aggregation and MS1 dispersed into the matrix instead of aggregating. The aggregation of hMSCs was attenuated by treatment with Rho kinase (ROCK) inhibitor and cadherin antibody. This reflected the close relationship between cell aggregation and migration with RhoA and cell-cell adhesion molecules. Angiogenic-specific gene expression profiles showed that expression of CD105 decreased to 22% in the ROCK inhibitor group compared to control group. These results showed that cell-based patterns in a 3D matrix are highly dependent on both cell aggregation and migration over time. (c) 2013, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 40 条
[1]   The effect of matrix characteristics on fibroblast proliferation in 3D gels [J].
Bott, Katrin ;
Upton, Zee ;
Schrobback, Karsten ;
Ehrbar, Martin ;
Hubbell, Jeffrey A. ;
Lutolf, Matthias P. ;
Rizzi, Simone C. .
BIOMATERIALS, 2010, 31 (32) :8454-8464
[2]   Direct-write bioprinting three-dimensional biohybrid systems for future regenerative therapies [J].
Chang, Carlos C. ;
Boland, Eugene D. ;
Williams, Stuart K. ;
Hoying, James B. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2011, 98B (01) :160-170
[3]   Bioprinting: inkjet printing proteins and hybrid cell-containing materials and structures [J].
Derby, Brian .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (47) :5717-5721
[4]   Secreted Frizzled-Related Protein-1 Enhances Mesenchymal Stem Cell Function in Angiogenesis and Contributes to Neovessel Maturation [J].
Dufourcq, Pascale ;
Descamps, Betty ;
Tojais, Nancy Ferreira ;
Leroux, Lionel ;
Oses, Pierre ;
Daret, Daniele ;
Moreau, Catherine ;
Lamaziere, Jean-Marie Daniel ;
Couffinhal, Thierry ;
Duplaa, Cecile .
STEM CELLS, 2008, 26 (11) :2991-3001
[5]   BMP-2, BMP-4, and PDGF-bb stimulate chemotactic migration of primary human mesenchymal progenitor cells [J].
Fiedler, J ;
Röderer, G ;
Günther, KP ;
Brenner, RE .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 87 (03) :305-312
[6]  
Foty RA, 1996, DEVELOPMENT, V122, P1611
[7]   The differential adhesion hypothesis: a direct evaluation [J].
Foty, RA ;
Steinberg, MS .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :255-263
[8]   Prespecification and plasticity: shifting mechanisms of cell migration [J].
Friedl, P .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (01) :14-23
[9]  
FRIEDL P, 1995, CANCER RES, V55, P4557
[10]   Collective cell migration in morphogenesis, regeneration and cancer [J].
Friedl, Peter ;
Gilmour, Darren .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (07) :445-457