CART (cocaine- and amphetamine-regulated transcript) peptide specific binding sites in PC12 cells have characteristics of CART peptide receptors
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24378198
DOI
10.1016/j.brainres.2013.12.024
PII: S0006-8993(13)01595-3
Knihovny.cz E-zdroje
- Klíčová slova
- Binding, CART peptide, Differentiation, PC12 cell, Signaling, c-Jun,
- MeSH
- acetylcholinesterasa analýza MeSH
- buňky PC12 MeSH
- hypothalamus účinky léků metabolismus MeSH
- kokainem a amfetaminem regulovaný transkript MeSH
- krysa rodu Rattus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nucleus solitarius účinky léků metabolismus MeSH
- proteiny nervové tkáně metabolismus farmakologie MeSH
- receptory peptidů metabolismus MeSH
- signální transdukce fyziologie MeSH
- vazebná místa MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetylcholinesterasa MeSH
- kokainem a amfetaminem regulovaný transkript MeSH
- proteiny nervové tkáně MeSH
- receptory peptidů MeSH
CART (cocaine- and amphetamine-regulated transcript) peptide is a neuropeptide with a powerful central anorexigenic effect. Specific CART peptide binding sites, most likely CART peptide receptors, have been found in PC12 cells. This study further characterizes the CART peptide binding sites in PC12 cells. After differentiation to a neuronal phenotype with nerve growth factor, the number of CART peptide binding sites in PC12 cells tripled. Following dexamethasone treatment, which transforms PC12 cells into chromaffin-like cells, the number of CART peptide binding sites substantially decreased. CART peptide did not affect the differentiation or acetylcholinesterase activity of PC12 cells, indicating that CART peptide does not participate in differentiation or neuronal activity. CART peptide increased the phosphorylation of SAPK/JNK (stress-activated protein kinase/c-Jun-amino-terminal kinase) and subsequent c-Jun protein expression. These effects were reversed by SP600125, a specific JNK-kinase inhibitor. CART peptide did not significantly affect ERK (extracellular signal-regulated kinase), CREB (cAMP responsive element binding protein), or p38 phosphorylation and c-Fos protein expression. Central administration of CART peptide into mice also resulted in increased c-Jun positive cells in dorsomedial hypothalamic nucleus and nucleus of the solitary tract, areas involved in food intake regulation. Activation of c-Jun by CART peptide might indicate a possible role of CART peptide in managing stress conditions rather than a role in cell proliferation or differentiation as well as the more complex and/or specific regulation ways by transcription factors in some nuclei involved in food intake regulation. The characteristics of stress that CART peptide potentially mediates should be further studied.
Citace poskytuje Crossref.org