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
. 2001 Nov;37(3):163-9.
doi: 10.1023/A:1020506821201.

In vitro culture of human chondrocytes (1): A novel enhancement action of ferrous sulfate on the differentiation of human chondrocytes

Affiliations

In vitro culture of human chondrocytes (1): A novel enhancement action of ferrous sulfate on the differentiation of human chondrocytes

M S Rahman et al. Cytotechnology. 2001 Nov.

Abstract

Chondrogenic differentiation of mesenchymal cells is generally thought to be initiated by the inductive action of specific growth factors and depends on intimate cell-cell interactions. The aim of our investigation was to characterize the influences of basic fibroblast growth factor (bFGF) and ferroussulfate (FeSO(4)) on proliferation and differentiation of human articular chondrocytes (HAC). This is the first report of the effects of FeSO(4) on chondrogenesis of HAC. Multiplied chondrocytes of hip and shoulder joints were cultured in chondrocyte growth medium supplemented with bFGF, FeSO(4), or both bFGF + FeSO(4) for4weeks. A 20 mul aliquot of a cell suspension containing2 x 10(7) cells ml(-1) was delivered onto each well of 24-well tissue culture plates. Cells cultured with the growth medium only was used as a control. Alamar blue and alcian blue staining were done to determine the chondrocyte proliferation and differentiation, respectively, after 4 weeks. The samples exposed to bFGF, FeSO(4), and combination of both indicated sufficient cell proliferation similar to the control level. Differentiations of the HAC exposed to bFGF, FeSO(4),and bFGF + FeSO(4) were 1.2-, 2.0-, and 2.2-fold of the control, respectively. Therefore, chondrocyte differentiation was significantly enhanced by the addition of FeSO(4) andbFGF + FeSO(4). The combined effects of bFGF and FeSO(4) were additive, rather than synergistic. These results suggest that treatment with ferrous sulfate alone or in combination with basic fibroblast growth factor etc, is a powerful tool to promote the differentiation of HAC for the clinical application.

PubMed Disclaimer

Similar articles

References

    1. Brown C.C., Balian G. Effect of heparin on synthesis of short chain collagen by chondrocytes and smooth muscle cells. J. Cell. Biol. 1987;105:1007–1012. doi: 10.1083/jcb.105.2.1007. - DOI - PMC - PubMed
    1. Bohme K., Conscience-Egli M., Tschan T., Winterhalter K.H., Bruckner P. Induction of proliferation or hypertrophy of chondrocytes in serum-free culture: the role of insulin-like growth factor-I, insulin, or thyroxine. J. Cell. Biol. 1992;116:1035–1042. doi: 10.1083/jcb.116.4.1035. - DOI - PMC - PubMed
    1. Bujia J., Sittinger M., Wilmes E., Hammer C. Effect of growth factors on cell proliferation by human nasal septal chondrocytes cultured in monolayer. Acta. Otolaryngol. 1994;114:539–543. - PubMed
    1. Bujia J., Pitzke P., Kastenbauer E., Wilmes E., Hammer C. Effect of growth factors on matrix synthesis by human nasal chondrocytes cultured in monolayer and in agar. Eur. Arch. Otorhinolaryngol. 1996;253:336–340. - PubMed
    1. Dreyfus J., Brunet-de Carvalho N., Duprez D., Raulais D., Vigny M. HB-GAM/ pleiotrophin but not RIHB/midkine enhances chondrogenesis in micromass culture. Exp. Cell. Res. 1998;241:171–180. doi: 10.1006/excr.1998.4040. - DOI - PubMed