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Research Article Free access | 10.1172/JCI113996

Transforming growth factor-beta. Murine glomerular receptors and responses of isolated glomerular cells.

K MacKay, L J Striker, J W Stauffer, T Doi, L Y Agodoa, and G E Striker

Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

Find articles by MacKay, K. in: PubMed | Google Scholar

Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

Find articles by Striker, L. in: PubMed | Google Scholar

Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

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Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

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Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

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Metabolic Disease Branch, National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland 20892.

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Published April 1, 1989 - More info

Published in Volume 83, Issue 4 on April 1, 1989
J Clin Invest. 1989;83(4):1160–1167. https://doi.org/10.1172/JCI113996.
© 1989 The American Society for Clinical Investigation
Published April 1, 1989 - Version history
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Abstract

Proliferation of resident glomerular cells and the accumulation of mesangial matrix are histologic abnormalities which are observed in the course of many progressive glomerular diseases. We explored the potential regulatory effects of transforming growth factor-beta (TGF-beta) on these processes. We found that cultured mouse glomerular endothelial, mesangial, and epithelial cells as well as isolated intact rat glomeruli possess high-affinity receptors for TGF-beta. We also found that, although TGF-beta consistently inhibited the proliferation of glomerular endothelial and epithelial cells, it acted as a bifunctional regulator of mesangial cell proliferation. TGF-beta significantly increased the production of collagen and fibronectin by glomerular mesangial cells whereas only fibronectin production was augmented in glomerular epithelial cells. The presence of TGF-beta receptors on intact glomeruli and on each glomerular cell type and the demonstrated responsiveness of these cells to TGF-beta combine to suggest that potentially important interactions may occur between resident glomerular cells and TGF-beta in vivo.

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