Effects of oxygen plasma treatment on adipose-derived human mesenchymal stem cell adherence to poly(L-lactic acid) scaffolds

被引:48
作者
Hanson, Ariel D.
Wall, Michelle E.
Pourdeyhimi, Behnam
Loboa, Elizabeth G.
机构
[1] N Carolina State Univ, Joint Dept Biomed Engn, Burlington Nucl Engn Labs 2142, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Nonwovens Cooperat Res Ctr, Raleigh, NC 27695 USA
关键词
hydrophilicity; non-woven PLLA scaffold; cell morphology; cell viability; melt-blown PLLA scaffold;
D O I
10.1163/156856207782246812
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Plasma treatment of substrate surfaces can be utilized to improve adhesion of cells to tissue-engineered scaffolds. The purpose of this study was to enhance cell adhesion to non-woven poly(L-lactic acid) (PLLA) scaffolds using oxygen plasma treatment to increase surface hydroxyl groups and thereby enhance substrate hydrophilicity. It was hypothesized that oxygen plasma treatment would increase the number of adipose-derived human mesenchymal stem cells (hMSCs) that adhered to melt-blown, non-woven PLLA scaffolds without affecting cell viability. The number of cells that adhered to the oxygen plasma-treated (10 min at 100 W) or untreated PLLA scaffolds was assessed at 2, 4, 8, 12, 24 and 48 h post-seeding via DNA analysis. Cell viability and morphology were also assessed at 2, 4, 8, 12 and 24 h post-seeding via a live/dead assay and hematoxylin staining, respectively. Oxygen plasma treatment decreased the contact angle of water from 75.6 degrees to 58.2 degrees, indicating an increase in the surface hydrophilicity of PLLA. The results of the DNA analysis indicated that there was an increased number of hMSCs on oxygen plasma treated scaffolds for two of the three donors. In addition, oxygen plasma treatment promoted a more even distribution of hMSCs throughout the scaffold and enhanced cell spreading at earlier time points without altering cell viability. This early induction of cell spreading and the uniform distribution of cells, in turn, may increase future proliferation and differentiation of hMSCs under conditions that simulate the microenvironment in vivo.
引用
收藏
页码:1387 / 1400
页数:14
相关论文
共 51 条
[1]   Modulating bone cells response onto starch-based biomaterials by surface plasma treatment and protein adsorption [J].
Alves, Catarina M. ;
Yang, Y. ;
Carnes, D. L. ;
Ong, J. L. ;
Sylvia, V. L. ;
Dean, D. D. ;
Agrawal, C. M. ;
Reis, R. L. .
BIOMATERIALS, 2007, 28 (02) :307-315
[2]   Using plasma deposits to promote cell population of the porous interior of three-dimensional poly(D,L-lactic acid) tissue-engineering scaffolds [J].
Barry, JJA ;
Silva, MMCG ;
Shakesheff, KM ;
Howdle, SM ;
Alexander, MR .
ADVANCED FUNCTIONAL MATERIALS, 2005, 15 (07) :1134-1140
[3]   Protein-coated poly(L-lactic acid) fibers provide a substrate for differentiation of human skeletal muscle cells [J].
Cronin, EM ;
Thurmond, FA ;
Bassel-Duby, R ;
Williams, RS ;
Wright, WE ;
Nelson, KD ;
Garner, HR .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (03) :373-381
[4]   Comparison of multi-lineage cells from human adipose tissue and bone marrow [J].
De Ugarte, DA ;
Morizono, K ;
Elbarbary, A ;
Alfonso, Z ;
Zuk, PA ;
Zhu, M ;
Dragoo, JL ;
Ashjian, P ;
Thomas, B ;
Benhaim, P ;
Chen, I ;
Fraser, J ;
Hedrick, MH .
CELLS TISSUES ORGANS, 2003, 174 (03) :101-109
[5]   A NOVEL PEPTIDE FROM AMYLOID P COMPONENT SUPPORTS CELL ATTACHMENT [J].
DHAWAN, S ;
FIELDS, RL ;
ROBEY, FA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (03) :1284-1290
[6]  
Gao JM, 1998, J BIOMED MATER RES, V42, P417, DOI 10.1002/(SICI)1097-4636(19981205)42:3<417::AID-JBM11>3.3.CO
[7]  
2-N
[8]  
Grinnell F, 1978, Int Rev Cytol, V53, P65
[9]   Surface protein characterization of human adipose tissue-derived stromal cells [J].
Gronthos, S ;
Franklin, DM ;
Leddy, HA ;
Robey, PG ;
Storms, RW ;
Gimble, JM .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 189 (01) :54-63
[10]   Clonal analysis of the differentiation potential of human adipose-derived adult stem cells [J].
Guilak, F ;
Lott, KE ;
Awad, HA ;
Cao, QF ;
Hicok, KC ;
Fermor, B ;
Gimble, JM .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 206 (01) :229-237