Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion
<p>Abstract</p> <p>Background</p> <p>Multiple neuropeptides, sometimes with opposing functions, can be produced from one precursor gene. To study the roles of the different neuropeptides encoded by one large precursor we developed a method to overexpress minigenes and e...
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doaj-85f79393a914456086eec23b54034edd2020-11-25T01:27:05ZengBMCBMC Neuroscience1471-22022010-08-011119410.1186/1471-2202-11-94Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretionde Backer Marijke WABrans Maike ADLuijendijk Mieneke CMGarner Keith Mvan den Heuvel Dianne MAPasterkamp R JeroenAdan Roger AH<p>Abstract</p> <p>Background</p> <p>Multiple neuropeptides, sometimes with opposing functions, can be produced from one precursor gene. To study the roles of the different neuropeptides encoded by one large precursor we developed a method to overexpress minigenes and establish local secretion.</p> <p>Results</p> <p>We fused the signal peptide from the Von Willebrand Factor (VWF) to a furin site followed by a processed form of the Agouti related protein (AgRP), AgRP<sub>83-132 </sub>or α-melanocyte stimulating hormone. <it>In vitro</it>, these minigenes were secreted and biologically active. Additionally, the proteins of the minigenes were not transported into projections of primary neurons, thereby ensuring local release. <it>In vivo </it>administration of VWF-AgRP<sub>83-132 </sub>, using an adeno-associated viral vector as a delivery vehicle, into the paraventricular hypothalamus increased body weight and food intake of these rats compared to rats which received a control vector.</p> <p>Conclusions</p> <p>This study demonstrated that removal of the N-terminal part of full length AgRP and addition of a VWF signal peptide is a successful strategy to deliver neuropeptide minigenes to the brain and establish local neuropeptide secretion.</p> http://www.biomedcentral.com/1471-2202/11/94 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
de Backer Marijke WA Brans Maike AD Luijendijk Mieneke CM Garner Keith M van den Heuvel Dianne MA Pasterkamp R Jeroen Adan Roger AH |
spellingShingle |
de Backer Marijke WA Brans Maike AD Luijendijk Mieneke CM Garner Keith M van den Heuvel Dianne MA Pasterkamp R Jeroen Adan Roger AH Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion BMC Neuroscience |
author_facet |
de Backer Marijke WA Brans Maike AD Luijendijk Mieneke CM Garner Keith M van den Heuvel Dianne MA Pasterkamp R Jeroen Adan Roger AH |
author_sort |
de Backer Marijke WA |
title |
Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion |
title_short |
Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion |
title_full |
Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion |
title_fullStr |
Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion |
title_full_unstemmed |
Neuropeptide delivery to the brain: a von Willebrand factor signal peptide to direct neuropeptide secretion |
title_sort |
neuropeptide delivery to the brain: a von willebrand factor signal peptide to direct neuropeptide secretion |
publisher |
BMC |
series |
BMC Neuroscience |
issn |
1471-2202 |
publishDate |
2010-08-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Multiple neuropeptides, sometimes with opposing functions, can be produced from one precursor gene. To study the roles of the different neuropeptides encoded by one large precursor we developed a method to overexpress minigenes and establish local secretion.</p> <p>Results</p> <p>We fused the signal peptide from the Von Willebrand Factor (VWF) to a furin site followed by a processed form of the Agouti related protein (AgRP), AgRP<sub>83-132 </sub>or α-melanocyte stimulating hormone. <it>In vitro</it>, these minigenes were secreted and biologically active. Additionally, the proteins of the minigenes were not transported into projections of primary neurons, thereby ensuring local release. <it>In vivo </it>administration of VWF-AgRP<sub>83-132 </sub>, using an adeno-associated viral vector as a delivery vehicle, into the paraventricular hypothalamus increased body weight and food intake of these rats compared to rats which received a control vector.</p> <p>Conclusions</p> <p>This study demonstrated that removal of the N-terminal part of full length AgRP and addition of a VWF signal peptide is a successful strategy to deliver neuropeptide minigenes to the brain and establish local neuropeptide secretion.</p> |
url |
http://www.biomedcentral.com/1471-2202/11/94 |
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