๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

In vitro tendon cell growth rates on a synthetic fiber scaffold material and on standard culture plates

โœ Scribed by Ricci, J. L. ;Gona, A. G. ;Alexander, H.


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
947 KB
Volume
25
Category
Article
ISSN
0021-9304

No coin nor oath required. For personal study only.

โœฆ Synopsis


Growth rates of rat tendon fibroblasts cultured in a three-dimensional carbon fiber matrix were compared with those of cells cultured on standard flat culture plates. The carbon fiber has been used as a tissue scaffold for tendon and ligament repair in animal and clinical studies. While cell growth on the culture plates appears to follow a growth curve containing a lag phase, a log phase, and plateau phase of growth, cell growth in the fiber matrix was characterized by a suppressed log phase of growth. SEM and cytotoxicity studies indicated that this effect was not caused by growth-inhibiting or cytotoxic substances from the carbon fiber. While we cannot rule out the possibility that cell growth was influenced by the surface chemistry of the carbon substrate, evidence from this and other studies suggests that the observed effect was caused by a lack of readily available surface area for cell attachment and growth on the small fibers. Because cell colonies growing on individual fibers are limited (at least in theory) to growing in two directions only, they enjoy limited opportunities for cell migration and growthin contrast with cell colonies on flat culture plates. These results suggest fundamental differences in the mechanisms controlling cell growth on planar vs. three-dimensional fiber substrates.


๐Ÿ“œ SIMILAR VOLUMES


In vitro tendon cell colony growth rates
โœ J. L. Ricci; H. Alexander; A. G. Gona; M. D. Lelah ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 590 KB

Effective integration of synthetic fiber scaffold materials into connective tissues depends to a great degree on tissue attachment and ingrowth into the material. The authors have developed an experimental model that utilizes rat tendon explants to test the rates of cell colony formation on differen