Flow cytometry analysis of human fetal osteoblast fate processes on spark plasma sintered hydroxyapatite-titanium biocomposites

被引:29
作者
Kumar, Alok [1 ]
Webster, Thomas J. [2 ]
Biswas, Krishanu [1 ]
Basu, Bikramjit [1 ,3 ]
机构
[1] Indian Inst Technol, Dept Mat Sci & Engn, Kanpur 208016, Uttar Pradesh, India
[2] Northeastern Univ, Coll Engn, Dept Chem Engn, Boston, MA 02115 USA
[3] Indian Inst Sci, Mat Res Ctr, Lab Biomat, Bangalore 560012, Karnataka, India
关键词
HA-Ti; flow cytometry; apoptosis; proliferation; cell cycle; IN-VITRO BIOACTIVITY; SURFACE-ROUGHNESS; CELL-CYCLE; ANNEXIN-V; BONE; COMPOSITES; APOPTOSIS; GROWTH; PHOSPHATIDYLSERINE; BIOCOMPATIBILITY;
D O I
10.1002/jbm.a.34603
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hydroxyapatite (HA)-based biocomposites have been widely investigated for a multitude of applications and these studies have been largely driven to improve mechanical properties (toughness and strength) without compromising cytocompatibility properties. Apart from routine cell viability/proliferation analysis, limited efforts have been made to quantify the fate processes (cell proliferation, cell cycle, and cell apoptosis) of human fetal osteoblast (hFOB) cells on HA-based composites, in vitro. In this work, the osteoblast cell fate process has been studied on a model hydroxyapatite-titanium (HA-Ti) system using the flow cytometry. In order to retain both HA and Ti, the novel processing technique, that is, spark plasma sintering, was suitably adopted. The cell fate processes of hFOBs, as evaluated using a flow cytometry, revealed statistically insignificant differences among HA-10 wt % Ti and HA and control (tissue culture polystyrene surface) in terms of osteoblast apoptosis, proliferation index as well as division index. For the first time, we provide quantified flow cytometry results to demonstrate that 10 wt % Ti additions to HA do not have any significant influence on the fate processes of human osteoblast-like cells, in vitro. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 101A:2925-2938, 2013.
引用
收藏
页码:2925 / 2938
页数:14
相关论文
共 73 条
[1]   Extracellular calcium regulates parathyroid hormone-related peptide expression in osteoblasts and osteoblast progenitor cells [J].
Ahlstrom, Mikael ;
Pekkinen, Minna ;
Riehle, Ulrike ;
Lamberg-Allardt, Christel .
BONE, 2008, 42 (03) :483-490
[2]   CELLULAR-ACTIVITY OF OSTEOBLASTS IN THE PRESENCE OF HYDROXYAPATITE - AN INVITRO EXPERIMENT [J].
ALLIOTLICHT, B ;
GREGOIRE, M ;
ORLY, I ;
MENANTEAU, J .
BIOMATERIALS, 1991, 12 (08) :752-756
[3]  
ANDREE HAM, 1990, J BIOL CHEM, V265, P4923
[4]  
[Anonymous], PREPARATION SYNTHETI
[5]  
[Anonymous], FLOW CYTOMETRY A S25
[6]  
[Anonymous], 2005, CULTURE ANIMAL CELLS, DOI DOI 10.1002/9780471747598
[7]  
[Anonymous], CHEM INDUCED CELL PR
[8]   The relative influence of the topography and chemistry of TiAl6V4 surfaces on osteoblastic cell behaviour [J].
Anselme, K ;
Linez, P ;
Bigerelle, M ;
Le Maguer, D ;
Le Maguer, A ;
Hardouin, P ;
Hildebrand, HF ;
Iost, A ;
Leroy, JM .
BIOMATERIALS, 2000, 21 (15) :1567-1577
[9]  
ARENDS MJ, 1991, INT REV EXP PATHOL, V32, P223
[10]  
Aubry JP, 1999, CYTOMETRY, V37, P197, DOI 10.1002/(SICI)1097-0320(19991101)37:3<197::AID-CYTO6>3.0.CO