Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1996;253(6):336-40.
doi: 10.1007/BF00178288.

Effect of growth factors on matrix synthesis by human nasal chondrocytes cultured in monolayer and in agar

Affiliations

Effect of growth factors on matrix synthesis by human nasal chondrocytes cultured in monolayer and in agar

J Bujía et al. Eur Arch Otorhinolaryngol. 1996.

Abstract

Reconstructive surgery of multiple areas of the body may require replacement bone or cartilage transplants to repair defects or lesions of skeletal tissue. Advances in cell and tissue culture techniques now permit synthesis of autologous human cartilage in vitro. Several growth factors regulate the metabolism and activation of cartilage cells. To enhance culture conditions and effectiveness for in vitro cartilage engineering, the aim of our investigations was to characterize the influence of transforming growth factor (TGF)-beta and basic fibroblast growth factor (bFGF) on human nasal septal chondrocytes. The isolated cells were cultured as monolayers on plastic and in soft agar. The biological effects of the growth factors were assessed by determining synthesis of total protein and proteoglycan. TGF-beta caused a dose-dependent stimulation of total protein as well as glycosaminoglycan synthesis by all chondrocytes cultured. This stimulatory effect of TGF-beta was greater for chondrocytes cultured in soft agar than for chondrocytes cultured on plastic. No stimulatory effects of matrix synthesis was observed for bFGF in either culture condition. Our results show that TGF-beta can be employed to enhance in vitro production of cartilage grafts for reconstructive surgery.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Plast Reconstr Surg. 1991 Nov;88(5):753-9 - PubMed
    1. Nature. 1974 May 10;249(453):123-7 - PubMed
    1. Endocrinology. 1975 Aug;97(2):359-65 - PubMed
    1. Calcif Tissue Int. 1988 Dec;43(6):352-8 - PubMed
    1. J Cell Physiol. 1987 Dec;133(3):491-8 - PubMed

Publication types

MeSH terms