Control over the Gradient Differentiation of Rat BMSCs on a PCL Membrane with Surface-Immobilized Alendronate Gradient

被引:56
作者
Zhu, Yang [1 ]
Mao, Zhengwei [1 ]
Gao, Changyou [1 ,2 ]
机构
[1] Zhejiang Univ, MOE Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
关键词
MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; BONE INSERTION SITE; IN-VITRO; OSTEOBLAST DIFFERENTIATION; SCAFFOLDS; POLYCAPROLACTONE; BISPHOSPHONATES; PROLIFERATION; DELIVERY;
D O I
10.1021/bm301523p
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Gradient biomaterials can offer progressively changing signals to specific tissue interface, and thereby modulate the conjunction between different tissues. A linear density gradient of alendronate (Aln), a molecule that is capable of promoting osteogenic differentiation of bone mesenchymal stem cells (BMSCs), was created on an aminolyzed poly(epsilon-caprolactone) (PCL) membrane. X-ray photoelectron spectroscopy and quartz crystal microbalance with dissipation revealed the linear increase of the Aln amount as a function of the position on the PCL membrane. By contrast, the surface wettability and energy were kept unchanged. The surface-grafted Aln showed a stronger ability to induce the osteogenic differentiation of rat BMSCs than its counterpart in culture medium of the same amount, and the osteo-inductive culture medium. On the Aln-grafted gradient surface, the BMSCs showed gradient osteogenic differentiation as a function of membrane position in terms of cell morphology, alkaline phosphatase activity, calcium deposition, and the expression of osteogenesis marker proteins including collagen type I (COL I), Runt-related transcription factor 2 (Runx2), and osteocalcin (OCN).
引用
收藏
页码:342 / 349
页数:8
相关论文
共 68 条
[1]
Balloni S, 2009, INT J ORAL MAX IMPL, V24, P627
[2]
Novel actions of bisphosphonates in bone: Preservation of osteoblast and osteocyte viability [J].
Bellido, Teresita ;
Plotkin, Lilian I. .
BONE, 2011, 49 (01) :50-55
[3]
Small functional groups for controlled differentiation of hydrogel-encapsulated human mesenchymal stem cells [J].
Benoit, Danielle S. W. ;
Schwartz, Michael P. ;
Durney, Andrew R. ;
Anseth, Kristi S. .
NATURE MATERIALS, 2008, 7 (10) :816-823
[4]
Polymeric growth factor delivery strategies for tissue engineering [J].
Chen, RR ;
Mooney, DJ .
PHARMACEUTICAL RESEARCH, 2003, 20 (08) :1103-1112
[5]
Spatio-temporal VEGF and PDGF delivery patterns blood vessel formation and maturation [J].
Chen, Ruth R. ;
Silva, Eduardo A. ;
Yuen, William W. ;
Mooney, David J. .
PHARMACEUTICAL RESEARCH, 2007, 24 (02) :258-264
[6]
The guidance of human mesenchymal stem cell differentiation in vitro by controlled modifications to the cell substrate [J].
Curran, Judith M. ;
Chen, Rui ;
Hunt, John A. .
BIOMATERIALS, 2006, 27 (27) :4783-4793
[7]
The control of human mesenchymal cell differentiation using nanoscale symmetry and disorder [J].
Dalby, Matthew J. ;
Gadegaard, Nikolaj ;
Tare, Rahul ;
Andar, Abhay ;
Riehle, Mathis O. ;
Herzyk, Pawel ;
Wilkinson, Chris D. W. ;
Oreffo, Richard O. C. .
NATURE MATERIALS, 2007, 6 (12) :997-1003
[8]
Emerging Techniques in Stratified Designs and Continuous Gradients for Tissue Engineering of Interfaces [J].
Dormer, Nathan H. ;
Berkland, Cory J. ;
Detamore, Michael S. .
ANNALS OF BIOMEDICAL ENGINEERING, 2010, 38 (06) :2121-2141
[9]
Drissi H, 2000, J CELL PHYSIOL, V184, P341, DOI 10.1002/1097-4652(200009)184:3<341::AID-JCP8>3.0.CO
[10]
2-Z