Melanocortin 4 receptor activates ERK-cFos pathway to increase brain-derived neurotrophic factor expression in rat astrocytes and hypothalamus. (15th August 2015)
- Record Type:
- Journal Article
- Title:
- Melanocortin 4 receptor activates ERK-cFos pathway to increase brain-derived neurotrophic factor expression in rat astrocytes and hypothalamus. (15th August 2015)
- Main Title:
- Melanocortin 4 receptor activates ERK-cFos pathway to increase brain-derived neurotrophic factor expression in rat astrocytes and hypothalamus
- Authors:
- Ramírez, D.
Saba, J.
Carniglia, L.
Durand, D.
Lasaga, M.
Caruso, C. - Abstract:
- Highlights: MC4R mechanisms of action were studied. MC4R-induced BDNF expression involves ERK and cFos activation in astrocytes and rat hypothalamus. Inhibition of PI3K, Src and RSK blocked MC4R-induced BDNF expression in astrocytes. Graphical Abstract: Abstract: Melanocortins are neuropeptides with well recognized anti-inflammatory and anti-apoptotic effects in the brain. Of the five melanocortin receptors (MCR), MC4R is abundantly expressed in the brain and is the only MCR present in astrocytes. We have previously shown that MC4R activation by the α-melanocyte stimulating hormone (α-MSH) analog, NDP-MSH, increased brain-derived neurotrophic factor (BDNF) expression through the classic cAMP–Protein kinase A–cAMP responsive element binding protein pathway in rat astrocytes. Now, we examined the participation of the mitogen activated protein kinases pathway in MC4R signaling. Rat cultured astrocytes treated with NDP-MSH 1 µM for 1 h showed increased BDNF expression. Inhibition of extracellular signal-regulated kinase (ERK) and ribosomal p90 S6 kinase (RSK), an ERK substrate, but not of p38 or JNK, prevented the increase in BDNF expression induced by NDP-MSH. Activation of MC4R increased cFos expression, a target of both ERK and RSK. ERK activation by MC4R involves cAMP, phosphoinositide-3 kinase (PI3K) and the non receptor tyrosine kinase, Src. Both PI3K and Src inhibition abolished NDP-MSH-induced BDNF expression. Moreover, we found that intraperitoneal injection of α-MSHHighlights: MC4R mechanisms of action were studied. MC4R-induced BDNF expression involves ERK and cFos activation in astrocytes and rat hypothalamus. Inhibition of PI3K, Src and RSK blocked MC4R-induced BDNF expression in astrocytes. Graphical Abstract: Abstract: Melanocortins are neuropeptides with well recognized anti-inflammatory and anti-apoptotic effects in the brain. Of the five melanocortin receptors (MCR), MC4R is abundantly expressed in the brain and is the only MCR present in astrocytes. We have previously shown that MC4R activation by the α-melanocyte stimulating hormone (α-MSH) analog, NDP-MSH, increased brain-derived neurotrophic factor (BDNF) expression through the classic cAMP–Protein kinase A–cAMP responsive element binding protein pathway in rat astrocytes. Now, we examined the participation of the mitogen activated protein kinases pathway in MC4R signaling. Rat cultured astrocytes treated with NDP-MSH 1 µM for 1 h showed increased BDNF expression. Inhibition of extracellular signal-regulated kinase (ERK) and ribosomal p90 S6 kinase (RSK), an ERK substrate, but not of p38 or JNK, prevented the increase in BDNF expression induced by NDP-MSH. Activation of MC4R increased cFos expression, a target of both ERK and RSK. ERK activation by MC4R involves cAMP, phosphoinositide-3 kinase (PI3K) and the non receptor tyrosine kinase, Src. Both PI3K and Src inhibition abolished NDP-MSH-induced BDNF expression. Moreover, we found that intraperitoneal injection of α-MSH induces BDNF and MC4R expression and activates ERK and cFos in male rat hypothalamus. Our results show for the first time that MC4R-induced BDNF expression in astrocytes involves ERK-RSK-cFos pathway which is dependent on PI3K and Src, and that melanocortins induce BDNF expression and ERK-cFos activation in rat hypothalamus. … (more)
- Is Part Of:
- Molecular and cellular endocrinology. Volume 411(2015)
- Journal:
- Molecular and cellular endocrinology
- Issue:
- Volume 411(2015)
- Issue Display:
- Volume 411, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 411
- Issue:
- 2015
- Issue Sort Value:
- 2015-0411-2015-0000
- Page Start:
- 28
- Page End:
- 37
- Publication Date:
- 2015-08-15
- Subjects:
- α-MSH α-melanocyte-stimulating hormone -- AC adenylate cyclase -- BDNF brain-derived neurotrophic factor -- CREB cAMP responsive element binding protein -- DAPI 4′, 6-diamido-2-phenylindole dihydrochloride -- ERK extracellular signal-regulated kinase -- GFAP glial fibrillary acidic protein -- GPCR G protein-coupled receptor -- HMB hypothalamic fragment -- HPRT hypoxanthine–guanine phosphoribosyltransferase -- MAPK mitogen activated protein kinase -- MCR melanocortin receptor -- NDP-MSH [Nle(4), D-Phe(7)]melanocyte-stimulating hormone -- PKA protein kinase A -- PI3K phosphoinositide-3 kinase -- PDK1 phosphoinositide-3-dependent protein kinase-1 -- Rp-cAMP Rp-adenosine 3′, 5′-cyclic monophosphorothioate triethylammonium -- RSK ribosomal p90 S6 kinase -- RT-qPCR reverse transcriptase- real time polymerase chain reaction
MC4R -- BDNF -- ERK -- cFos -- Astrocytes -- Hypothalamus
Endocrinology -- Periodicals
Molecular biology -- Periodicals
Cytology -- Periodicals
Endocrinology -- Periodicals
Hormones -- Periodicals
Endocrinologie -- Périodiques
Cytology
Endocrinology
Molecular biology
Periodicals
573.4 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03037207 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.mce.2015.04.008 ↗
- Languages:
- English
- ISSNs:
- 0303-7207
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- Legaldeposit
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