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Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide

BACKGROUND: The survival promoting peptide Y-P30 has a variety of neuritogenic and neuroprotective effects in vitro and in vivo. In previous work we reported the expression of Y-P30/dermcidin in maternal peripheral blood mononuclear cells (PBMCs) and the transport of the protein to the fetal brain....

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Autores principales: Mikhaylova, Marina, Schumacher, Anne, Borutzki, Corinna, Neumann, Janine R, Macharadze, Tamar, El-Mousleh, Tarek, Wahle, Petra, Zenclussen, Ana C, Kreutz, Michael R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082292/
https://www.ncbi.nlm.nih.gov/pubmed/24969620
http://dx.doi.org/10.1186/1756-0500-7-400
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author Mikhaylova, Marina
Schumacher, Anne
Borutzki, Corinna
Neumann, Janine R
Macharadze, Tamar
El-Mousleh, Tarek
Wahle, Petra
Zenclussen, Ana C
Kreutz, Michael R
author_facet Mikhaylova, Marina
Schumacher, Anne
Borutzki, Corinna
Neumann, Janine R
Macharadze, Tamar
El-Mousleh, Tarek
Wahle, Petra
Zenclussen, Ana C
Kreutz, Michael R
author_sort Mikhaylova, Marina
collection PubMed
description BACKGROUND: The survival promoting peptide Y-P30 has a variety of neuritogenic and neuroprotective effects in vitro and in vivo. In previous work we reported the expression of Y-P30/dermcidin in maternal peripheral blood mononuclear cells (PBMCs) and the transport of the protein to the fetal brain. In this study we analyzed hormonal regulation of Y-P30 in human immune cells and expression of Y-P30 in the placenta. We further studied the stability and secretion of the Y-P30 peptide. RESULTS: We found indications that Y-P30 might be produced in human placenta. The Y-P30 mRNA was rarely found in isolated human PBMCs and alpha-feto-protein, human chorionic gonadotropin as well as estradiol combined with progesterone could not induce Y-P30 expression. Y-P30 was found to be extraordinarily stable; therefore, contamination with the peptide and the Y-P30/Dermcidin precursor mRNA is a serious concern in experiments looking at the expression of Y-P30/Dermcidin. In cultured cell lines and primary neurons we found that Y-P30 could be released, but neuronal uptake of Y-P30 was not observed. CONCLUSIONS: Our data suggest that a source of Y-P30 apart from eccrine glands might be the placenta. The peptide can be secreted together with the signaling peptide and it might reach the fetal brain where it can exert its neuritogenic functions by binding to neuronal membranes.
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spelling pubmed-40822922014-07-05 Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide Mikhaylova, Marina Schumacher, Anne Borutzki, Corinna Neumann, Janine R Macharadze, Tamar El-Mousleh, Tarek Wahle, Petra Zenclussen, Ana C Kreutz, Michael R BMC Res Notes Research Article BACKGROUND: The survival promoting peptide Y-P30 has a variety of neuritogenic and neuroprotective effects in vitro and in vivo. In previous work we reported the expression of Y-P30/dermcidin in maternal peripheral blood mononuclear cells (PBMCs) and the transport of the protein to the fetal brain. In this study we analyzed hormonal regulation of Y-P30 in human immune cells and expression of Y-P30 in the placenta. We further studied the stability and secretion of the Y-P30 peptide. RESULTS: We found indications that Y-P30 might be produced in human placenta. The Y-P30 mRNA was rarely found in isolated human PBMCs and alpha-feto-protein, human chorionic gonadotropin as well as estradiol combined with progesterone could not induce Y-P30 expression. Y-P30 was found to be extraordinarily stable; therefore, contamination with the peptide and the Y-P30/Dermcidin precursor mRNA is a serious concern in experiments looking at the expression of Y-P30/Dermcidin. In cultured cell lines and primary neurons we found that Y-P30 could be released, but neuronal uptake of Y-P30 was not observed. CONCLUSIONS: Our data suggest that a source of Y-P30 apart from eccrine glands might be the placenta. The peptide can be secreted together with the signaling peptide and it might reach the fetal brain where it can exert its neuritogenic functions by binding to neuronal membranes. BioMed Central 2014-06-26 /pmc/articles/PMC4082292/ /pubmed/24969620 http://dx.doi.org/10.1186/1756-0500-7-400 Text en Copyright © 2014 Mikhaylova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Mikhaylova, Marina
Schumacher, Anne
Borutzki, Corinna
Neumann, Janine R
Macharadze, Tamar
El-Mousleh, Tarek
Wahle, Petra
Zenclussen, Ana C
Kreutz, Michael R
Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title_full Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title_fullStr Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title_full_unstemmed Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title_short Analysis of Y-P30/Dermcidin expression and properties of the Y-P30 peptide
title_sort analysis of y-p30/dermcidin expression and properties of the y-p30 peptide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082292/
https://www.ncbi.nlm.nih.gov/pubmed/24969620
http://dx.doi.org/10.1186/1756-0500-7-400
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