Control of rat glomerular epithelial cell growth in vitro View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1990-04

AUTHORS

Stephen Adler, X. Chen, B. Eng

ABSTRACT

The interaction of cultured rat GEC1 with several growth factors was explored in order to obtain a better understanding of in vivo factors which might stimulate GEC proliferation. GEC proliferated in response to EGF but not IGF-1, MSA or PDGF. Specific, saturable receptors for EGF were detected in saturation and competition binding studies utilizing 125I-EGF with an approximate Kd of 1.7 nM and 86,000 binding sites per cell. TGF-beta inhibited GEC growth in a time and dose dependent manner with a brief early exposure resulting in prolonged growth inhibition which was not reversible by EGF. Exposure to TGF-beta sufficient to maximally inhibit growth had no effect on EGF binding to GEC. More prolonged exposure to TGF-beta, however, did result in an increase in the apparent number of EGF receptors on GEC but no change in Kd. These studies suggest that EGF and TGF-beta released by inflammatory cells or platelets during the course of glomerular injury may play a role in modulating glomerular cell proliferation. More... »

PAGES

1048-1054

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ki.1990.84

DOI

http://dx.doi.org/10.1038/ki.1990.84

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035763377

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2342243


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