| Literature DB >> 11432592 |
H Ueno1, F Nakamura, M Murakami, M Okumura, T Kadosawa, T Fujinag.
Abstract
Chitosan is reported as an accelerator of wound healing. Histological findings of previous reports indicate that chitosan accelerates the reformation of connective tissue, however the details of the mechanism are not clear. In this study, firstly L929 mouse fibroblasts were cultured with chitosan and the production of extracellular matrix (ECM) was evaluated in vitro. Type I and III collagens and fibronectin were secreted by L929 with or without chitosan; however there was no significant difference in the amount of ECM between the control and the chitosan groups. Secondly, macrophages were stimulated with chitosan, and then transforming growth factor-beta 1 (TGF-beta1) and platelet-derived growth factor (PDGF) messenger ribonucleic acid (mRNA) expressions and production of their proteins were assayed in vitro. As a result, chitosan promoted the production of TGF-beta1 and PDGF. These results indicate that chitosan does not directly accelerate ECM production by fibroblast and the ECM production may increase by the growth factors.Entities:
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Year: 2001 PMID: 11432592 DOI: 10.1016/s0142-9612(00)00401-4
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479