Effect of Fiber Diameter on Proliferation and Differentiation of MC3T3-E1 Pre-Osteoblasts

被引:19
作者
Guo, Zhenzhao [1 ]
Ma, Min [2 ]
Huang, Xun [1 ]
Li, Hong [1 ]
Zhou, Changren [1 ]
机构
[1] Jinan Univ, Dept Mat Sci & Engn, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Coll Med, Guangzhou 510632, Guangdong, Peoples R China
关键词
Osteoblast; Architecture; Tissue Engineering; Scaffold Design; ELECTROSPUN POLY(D; L-LACTIC-CO-GLYCOLIC ACID); NANOFIBROUS SCAFFOLDS; CELLS; BONE; MORPHOLOGY; MESHES; SIZE;
D O I
10.1166/jbt.2017.1548
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In the design of proper scaffolds for tissue engineering, the bulk material properties and scaffold architecture are fundamental because the scaffolds have been shown to have an essential role in the induction of cell adhesion and mediation of cellular behavior. It is popularly accepted that the surface topography (shape, size, and surface texture) is one of the most vital cues that influences cellular reactions in vivo and cell-material interactions in vitro. The objective of this study was to better understand the impact of topography on MC3T3-E1 pre-osteoblasts' response to the co-culture of electrospun fibrous scaffolds. Three kinds of biomimetic scaffolds with typical average fiber diameters of 0.347 mu m, 0.947 mu m, and 6.48 mu m were fabricated by adjusting proper electrospinning conditions. Cell morphology, proliferation, ALP activity, and gene expression of MC3T3-E1 cells cultured on the scaffolds were studied. Cells cultured on 0.35 mu m scaffolds showed a higher projected area and upregulation of osteogenic phenotype gene, such as Runx2, Col I, ALP, and OCN. For cells cultured on 6.5 mu m scaffolds, a higher proliferation rate and aspect ratio were noted. Our results showed that topographical cues designed into scaffolds can regulate proliferation and differentiation of osteoblastic cells.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 36 条
[1]  
Allison C.B., 2015, BIOMED MATER, V10
[2]   Effect of fiber diameter on spreading, proliferation, and differentiation of osteoblastic cells on electrospun poly(lactic acid) substrates [J].
Badami, AS ;
Kreke, MR ;
Thompson, MS ;
Riffle, JS ;
Goldstein, AS .
BIOMATERIALS, 2006, 27 (04) :596-606
[3]   Effect of fiber diameter and orientation on fibroblast morphology and proliferation on electrospun poly(D,L-lactic-co-glycolic acid) meshes [J].
Bashur, Chris A. ;
Dahlgren, Linda A. ;
Goldstein, Aaron S. .
BIOMATERIALS, 2006, 27 (33) :5681-5688
[4]   Effect of Fiber Diameter and Alignment of Electrospun Polyurethane Meshes on Mesenchymal Progenitor Cells [J].
Bashur, Chris A. ;
Shaffer, Robyn D. ;
Dahlgren, Linda A. ;
Guelcher, Scott A. ;
Goldstein, Aaron S. .
TISSUE ENGINEERING PART A, 2009, 15 (09) :2435-2445
[5]   Polymer nanofibrous structures: Fabrication, biofunctionalization, and cell interactions [J].
Beachley, Vince ;
Wen, Xuejun .
PROGRESS IN POLYMER SCIENCE, 2010, 35 (07) :868-892
[6]   Electrospun fibre diameter, not alignment, affects mesenchymal stem cell differentiation into the tendon/ligament lineage [J].
Cardwell, Robyn D. ;
Dahlgren, Linda A. ;
Goldstein, Aaron S. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2014, 8 (12) :937-945
[7]   Osteogenic lineage restriction by osteoprogenitors cultured on nanometric grooved surfaces: The role of focal adhesion maturation [J].
Cassidy, John W. ;
Roberts, Jemma N. ;
Smith, Carol-Anne ;
Robertson, Mary ;
White, Kate ;
Biggs, Manus J. ;
Oreffo, Richard O. C. ;
Dalby, Matthew J. .
ACTA BIOMATERIALIA, 2014, 10 (02) :651-660
[8]   Gas-Foamed Scaffold Gradients for Combinatorial Screening in 3D [J].
Chatterjee, Kaushik ;
Kraigsley, Alison M. ;
Bolikal, Durgadas ;
Kohn, Joachim ;
Simon, Carl G., Jr. .
JOURNAL OF FUNCTIONAL BIOMATERIALS, 2012, 3 (01) :173-182
[9]  
Choi JY, 1996, J CELL BIOCHEM, V61, P609, DOI 10.1002/(SICI)1097-4644(19960616)61:4<609::AID-JCB15>3.0.CO
[10]  
2-A