Biocompatibility of NDGA-polymerized collagen fibers. II. Attachment, proliferation, and migration of tendon fibroblasts in vitro

Citation
Tj. Koob et al., Biocompatibility of NDGA-polymerized collagen fibers. II. Attachment, proliferation, and migration of tendon fibroblasts in vitro, J BIOMED MR, 56(1), 2001, pp. 40-48
Citations number
41
Categorie Soggetti
Multidisciplinary
Journal title
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH
ISSN journal
00219304 → ACNP
Volume
56
Issue
1
Year of publication
2001
Pages
40 - 48
Database
ISI
SICI code
0021-9304(200107)56:1<40:BONCFI>2.0.ZU;2-M
Abstract
The material properties of collagen fibers polymerized with nordihydroguaia retic acid (NDGA) are equivalent to native tendon, suggesting that NDGA cro sslinking may provide a viable approach to stabilizing collagenous material s for use in repairing ruptured, lacerated, or surgically transected fibrou s tissues, such as tendons and ligaments (Koob & Hemandez, Biomaterials, in press). The present study evaluated the biocompatibility of these fibers w ith cultured bovine tendon fibroblasts. Fibroblast attachment, migration, a nd proliferation on NDGA-crosslinked materials were compared to those on pr epolymerized type I tendon collagen constructs as well as on tissue-culture -treated plastic. Fibroblast attachment on NDGA-crosslinked collagen fibril s was equivalent to attachment on plates coated with collagen alone. Over a period of 8 days in culture, attached fibroblasts proliferated on NDGA-cro sslinked collagen at a rate identical to that of fibroblasts attached to na tive collagen, in order for the biomaterial effectively to bridge gaps in f ibrous tissues, fibroblasts must be able to migrate and replicate on the br idging fiber. Control and crosslinked fibers were inserted in calf tendon e xplants, with a portion of the fiber extending out of the sectioned end of the tendon. Explants were cultured for 9 weeks, and the number of cells was measured at weekly intervals. Cells appeared on the fibers after 1 week of culture. By 2 weeks, cells had colonized the entire fiber. The number of c ells continued to increase throughout the 9 weeks in culture, forming a lay er several cells thick. Histologic analysis indicated that the fibroblasts populating the fibers appeared to originate in the epitenon. There was no d ifference in the rate of fibroblast migration and replication, nor in the u ltimate number of colonizing cells, between control collagen fibers and NDG A-crosslinked fibers. NDGA-crosslinked fibers may provide a means of bridgi ng gaps in ruptured, lacerated, or surgically transected tendons by providi ng a mechanically competent scaffold on which tendon fibroblasts can migrat e, attach, and proliferate. (C) 2001 John Wiley & Sons, Inc.