Differential expression of the keratinocyte growth factor (KGF) and KGF receptor genes in human vascular smooth muscle cells and arteries
Autor: | Jeffrey S. Rubin, Gregory F. Alberts, Jeffrey A. Winkles, Sabina DeMartino, Marcio Chedid, William G. Taylor |
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Rok vydání: | 1997 |
Předmět: |
medicine.medical_specialty
Vascular smooth muscle Physiology medicine.medical_treatment Clinical Biochemistry Cell Cell Biology Biology Fibroblast growth factor Cell biology chemistry.chemical_compound Paracrine signalling Cytokine medicine.anatomical_structure Endocrinology chemistry Internal medicine Gene expression medicine Keratinocyte growth factor Northern blot |
Zdroj: | Journal of Cellular Physiology. 173:380-386 |
ISSN: | 1097-4652 0021-9541 |
DOI: | 10.1002/(sici)1097-4652(199712)173:3<380::aid-jcp10>3.0.co;2-g |
Popis: | Keratinocyte growth factor (KGF) is a secreted member of the fibroblast growth factor (FGF) family of heparin-binding proteins. Studies reported to date indicate that it functions primarily as an important paracrine mediator of epithelial cell growth and differentiation. KGF appears to act via binding to a specific FGF receptor-2 isoform generated by an alternative splicing mechanism. To determine whether KGF may play a role in vascular smooth muscle cell (SMC) biology, we investigated KGF and KGF receptor gene expression in human SMC cultured in vitro as well as in several human nonatherosclerotic artery and atheroma specimens. KGF mRNA but not KGF receptor mRNA was expressed by SMCs, as determined by Northern blot hybridization analysis or reverse transcription-polymerase chain reaction assays, respectively. Additional experiments demonstrated that 1) human SMCs produce and secrete mitogenically active KGF and that 2) the cytokine interleukin-1 increases KGF mRNA and protein levels in human SMCs. We also found that KGF transcripts but not KGF receptor transcripts were expressed in control and atherosclerotic human arteries. Taken together, these results indicate that KGF is unlikely to be involved in SMC growth regulation unless it can function intracellularly or interact with a presently unidentified KGF receptor. |
Databáze: | OpenAIRE |
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