A Chimera between Platelet-Derived Growth Factorβ-Receptor and Fibroblast Growth Factor Receptor-1 Stimulates Pancreaticβ-Cell. DNA Synthesis in the Presence of PDGF-BB
作者:
MaresJaroslav,
ClaessonLena,
WelshMichael,
期刊:
Growth Factors
(Taylor Available online 1992)
卷期:
Volume 6,
issue 2
页码: 93-101
ISSN:0897-7194
年代: 1992
DOI:10.3109/08977199209011013
出版商: Taylor&Francis
关键词: islets;chimeric receptor;DNA synthesis
数据来源: Taylor
摘要:
AbstractThis study was undertaken to characterize the expression of a chimeric growth factor receptor composed of the extracellular and transmembrane domains of the platelet-derived growth factor (PDGF)β-receptor (PDGFR-β) fused to the intracellular domain of the fibroblast growth factor receptor-1 (FGFR-1) and to assess its effect on the growth potential of pancreatic islet cells. For this purpose rat pancreatic islets or monolayers of pancreatic islet cells were transfected with recombinant DNA constructs coding for the PDGF B-chain, the PDGFR-β, the FGFR-1 and the chimera between PDGFR-βand FGFR-1. DNA synthesis, monitored as the percentage of labelled nuclei and [3H]thymidine incorporation, was stimulated in pancreatic islet cells cotransfected with the constructs coding for the PDGF B-chain and the PDGFR-βor the chimeric PDGFR-β/FGFR-1 as compared with that determined after transfection with control plasmid. PDGF-BB stimulated DNA synthesis when islet cells had been transfected with PDGFR-βor PDGFR-β/FGFR-1. Cotransfection of the PDGFR-βand the chimeric PDGFR-β/FGFR-1 constructs attenuated the stimulation of DNA synthesis in response to PDGF-BB. Receptor binding studies showed binding with a Kdof 0.7 nM to the chimeric receptor. The present findings show that when the chimeric PDGFR-β/FGFR-1 construct is expressed inβ-cells it is efficient in increasing DNA synthesis when stimulated with ligand.
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