Nanoscale definition of substrate materials to direct human adult stem cells towards tissue specific populations

被引:23
作者
Curran, Judith M. [1 ]
Chen, Rui [1 ]
Stokes, Robert [2 ]
Irvine, Eleanor [2 ]
Graham, Duncan [2 ]
Gubbins, Earl [3 ]
Delaney, Deany [3 ]
Amro, Nabil [3 ]
Sanedrin, Raymond [3 ]
Jamil, Haris [3 ]
Hunt, John A. [1 ]
机构
[1] Univ Liverpool, UKCTE, UKBioTEC, LINSET, Liverpool L69 3GA, Merseyside, England
[2] Univ Strathclyde, Dept Pure & Appl Chem, Ctr Mol Nanometrol, WestCHEM, Glasgow, Lanark, Scotland
[3] NanoInk Inc, Skokie, IL 60077 USA
基金
英国医学研究理事会;
关键词
ADHESION; FIBRONECTIN; COMPLEX;
D O I
10.1007/s10856-009-3976-x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The development of homogenously nano-patterned chemically modified surfaces that can be used to initiate a cellular response, particularly stem cell differentiation, in a highly controlled manner without the need for exogenous biological factors has never been reported, due to that fact that precisely defined and reproducible systems have not been available that can be used to study cell/material interactions and unlock the potential of a material driven cell response. Until now material driven stem cell (furthermore any cell) responses have been variable due to the limitations in definition and reproducibility of the underlying substrate and the lack of true homogeneity of modifications that can dictate a cellular response at a sub-micron level that can effectively control initial cell interactions of all cells that contact the surface. Here we report the successful design and use of homogenously molecularly nanopatterned surfaces to control initial stem cell adhesion and hence function. The highly specified nano-patterned arrays were compared directly to silane modified bulk coated substrates that have previously been proven to initiate mesenchymal stem cell (MSC) differentiation in a heterogenous manner, the aim of this study was to prove the efficiency of these previously observed cell responses could be enhanced by the incorporation of nano-patterns. Nano-patterned surfaces were prepared by Dip Pen Nanolithography(A (R)) (DPNA (R)) to produce arrays of 70 nm sized dots separated by defined spacings of 140, 280 and 1000 nm with terminal functionalities of carboxyl, amino, methyl and hydroxyl and used to control cell growth. These nanopatterned surfaces exhibited unprecedented control of initial cell interactions and will change the capabilities for stem cell definition in vitro and then cell based medical therapies. In addition to highlighting the ability of the materials to control stem cell functionality on an unprecedented scale this research also introduces the successful scale-up of DPNA (R) and the novel chemistries and systems to facilitate the production of homogeneously patterned substrates (5 mm(2)) that are applicable for use in in vitro cell conditions over prolonged periods for complete control of material driven cell responses.
引用
收藏
页码:1021 / 1029
页数:9
相关论文
共 16 条
[1]   Increased osteoblast adhesion on nanograined Ti modified with KRSR [J].
Balasundaram, Ganesan ;
Webster, Thomas J. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 80A (03) :602-611
[2]   Micro and nano-structured surfaces [J].
Barbucci, R ;
Pasqui, D ;
Wirsen, A ;
Affrossman, S ;
Curtis, A ;
Tetta, C .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2003, 14 (08) :721-725
[3]   Protein repellent properties of covalently attached PEG coatings on nanostructured SiO2-based interfaces [J].
Bluemmel, Jacques ;
Perschmann, Nadine ;
Aydin, Daniel ;
Drinjakovic, Jovana ;
Surrey, Thomas ;
Lopez-Garcia, Monica ;
Kessler, Horst ;
Spatz, Joachim P. .
BIOMATERIALS, 2007, 28 (32) :4739-4747
[4]   Cell spreading and focal adhesion dynamics are regulated by spacing of integrin ligands [J].
Cavalcanti-Adam, Elisabetta Ada ;
Volberg, Tova ;
Micoulet, Alexandre ;
Kessler, Horst ;
Geiger, Benjamin ;
Spatz, Joachim Pius .
BIOPHYSICAL JOURNAL, 2007, 92 (08) :2964-2974
[5]  
Cavalcanti-Adam Elisabetta Ada, 2005, Prog Orthod, V6, P232
[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]   Expansion of human chondrocytes in an intermittent stirred flow bioreactor, using modified biodegradable microspheres [J].
Curran, SJ ;
Chen, R ;
Curran, JM ;
Hunt, JA .
TISSUE ENGINEERING, 2005, 11 (9-10) :1312-1322
[8]   Nanoprinting onto cells [J].
Curtis, Adam S. G. ;
Dalby, Matthew J. ;
Gadegaard, Nikolaj .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2006, 3 (08) :393-398
[9]   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
[10]   Force sensing and generation in cell phases:: analyses of complex functions [J].
Döbereiner, HG ;
Dubin-Thaler, BJ ;
Giannone, G ;
Sheetz, MP .
JOURNAL OF APPLIED PHYSIOLOGY, 2005, 98 (04) :1542-1546