Cell population dynamics modulate the rates of tissue growth processes

被引:76
作者
Cheng, G
Youssef, BB
Markenscoff, P
Zygourakis, K [1 ]
机构
[1] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77251 USA
[2] Univ Houston, Dept Elect & Comp Engn, Houston, TX 77204 USA
关键词
D O I
10.1529/biophysj.105.063701
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The development and testing of a discrete model describing the dynamic process of tissue growth in three-dimensional scaffolds is presented. The model considers populations of cells that execute persistent random walks on the computational grid, collide, and proliferate until they reach confluence. To isolate the effect of population dynamics on tissue growth, the model assumes that nutrient and growth factor concentrations remain constant in space and time. Simulations start either by distributing the seed cells uniformly and randomly throughout the scaffold, or from an initial condition designed to simulate the migration and cell proliferation phase of wound healing. Simulations with uniform seeding show that cell migration enhances tissue growth by counterbalancing the adverse effects of contact inhibition. This beneficial effect, however, diminishes and disappears completely for large migration speeds. By contrast, simulations with the "wound" seeding mode show a continual enhancement of tissue regeneration rates with increasing cell migration speeds. We conclude that cell locomotory parameters and the spatial distribution of seed cells can have profound effects on the dynamics of the process and, consequently, on the pattern and rates of tissue growth. These results can guide the design of experiments for testing the effectiveness of biomimetic modi. cations for stimulating tissue growth.
引用
收藏
页码:713 / 724
页数:12
相关论文
共 78 条
[51]   Growing new organs [J].
Mooney, DJ ;
Mikos, AG .
SCIENTIFIC AMERICAN, 1999, 280 (04) :60-65
[52]   Contact-dependent inhibition of angiogenesis by cardiac fibroblasts in three-dimensional fibrin gels in vitro: implications for microvascular network remodeling and coronary collateral formation [J].
Nehls, V ;
Herrmann, R ;
Huhnken, M ;
Palmetshofer, A .
CELL AND TISSUE RESEARCH, 1998, 293 (03) :479-488
[53]   Locomotory phenotypes of human tumor cell lines and T lymphocytes in a three-dimensional collagen lattice [J].
Niggemann, B ;
Maaser, K ;
Lu, HQ ;
Kroczek, R ;
Zanker, KS ;
Friedl, P .
CANCER LETTERS, 1997, 118 (02) :173-180
[54]  
Noble P.B., 1986, COMPUTER ASSISTED AN
[55]   A model for individual and collective cell movement in Dictyostelium discoideum [J].
Palsson, E ;
Othmer, HG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10448-10453
[56]  
Puchelle E, 2000, Acta Otorhinolaryngol Belg, V54, P263
[57]   Bioreactors and bioprocessing for tissue engineering [J].
Ratcliffe, A ;
Niklason, LE .
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS, 2002, 961 :210-215
[58]   Hydrogel-coated textile scaffolds as three-dimensional growth support for human umbilical vein endothelial cells (HUVECs): Possibilities as coculture system in liver tissue engineering [J].
Risbud, MV ;
Karamuk, E ;
Moser, R ;
Mayer, J .
CELL TRANSPLANTATION, 2002, 11 (04) :369-377
[59]   MONITORING AND MODELING DENSITY-DEPENDENT GROWTH OF ANCHORAGE-DEPENDENT CELLS [J].
RUAAN, RC ;
TSAI, GJ ;
TSAO, GT .
BIOTECHNOLOGY AND BIOENGINEERING, 1993, 41 (03) :380-389
[60]   Concentric cylinder bioreactor for production of tissue engineered cartilage: Effect of seeding density and hydrodynamic loading on construct development [J].
Saini, S ;
Wick, TM .
BIOTECHNOLOGY PROGRESS, 2003, 19 (02) :510-521