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Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis

BACKGROUND: Activity-dependent neuroprotector (ADNP) is a neuroprotective molecule containing an 8-amino acid peptide, NAPVSIPQ (NAP), that is sufficient for its neuroprotective effects. OBJECTIVE: To assess the expression of ADNP in the human immune system in normal subjects and multiple sclerosis...

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Autores principales: Braitch, Manjit, Kawabe, Kiyokazu, Nyirenda, Mukanthu, Gilles, Lucie Jean, Robins, R. Adrian, Gran, Bruno, Murphy, Sean, Showe, Louise, Constantinescu, Cris S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701887/
https://www.ncbi.nlm.nih.gov/pubmed/19923857
http://dx.doi.org/10.1159/000258695
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author Braitch, Manjit
Kawabe, Kiyokazu
Nyirenda, Mukanthu
Gilles, Lucie Jean
Robins, R. Adrian
Gran, Bruno
Murphy, Sean
Showe, Louise
Constantinescu, Cris S.
author_facet Braitch, Manjit
Kawabe, Kiyokazu
Nyirenda, Mukanthu
Gilles, Lucie Jean
Robins, R. Adrian
Gran, Bruno
Murphy, Sean
Showe, Louise
Constantinescu, Cris S.
author_sort Braitch, Manjit
collection PubMed
description BACKGROUND: Activity-dependent neuroprotector (ADNP) is a neuroprotective molecule containing an 8-amino acid peptide, NAPVSIPQ (NAP), that is sufficient for its neuroprotective effects. OBJECTIVE: To assess the expression of ADNP in the human immune system in normal subjects and multiple sclerosis patients. MATERIALS AND METHODS: ADNP expression was assessed in peripheral blood mononuclear cells (PBMCs) from healthy donors and multiple sclerosis (MS) patients using staining with anti-ADNP (NAP) antibodies and markers for T cells, B cells, monocytes and natural killer cells. ADNP mRNA was determined in peripheral blood from MS patients (n = 24) and matched controls (n = 21). Expression of activation markers CD69 and CD154 and of IFN-γ was assessed by flow cytometry in stimulated PBMCs. Effects of NAP on immune cell proliferation was assessed by tritiated thymidine incorporation. RESULTS: Monocytes, B cells and T cells, but not regulatory (CD4+CD25+) T cells expressed ADNP. NAP peptide decreased the expression of CD69, CD154 and IFN-γ in PBMC and caused suppressed anti-CD3-/anti-CD28-stimulated PBMC proliferation. ADNP mRNA was reduced in MS compared to control peripheral blood. CONCLUSION: ADNP is expressed in many immune system cells. ADNP mRNA is reduced in PBMCs in MS. The peptide NAP, which plays an important role in neuroprotection, has potential immunomodulatory properties.
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spelling pubmed-37018872013-07-11 Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis Braitch, Manjit Kawabe, Kiyokazu Nyirenda, Mukanthu Gilles, Lucie Jean Robins, R. Adrian Gran, Bruno Murphy, Sean Showe, Louise Constantinescu, Cris S. Neuroimmunomodulation Original Paper BACKGROUND: Activity-dependent neuroprotector (ADNP) is a neuroprotective molecule containing an 8-amino acid peptide, NAPVSIPQ (NAP), that is sufficient for its neuroprotective effects. OBJECTIVE: To assess the expression of ADNP in the human immune system in normal subjects and multiple sclerosis patients. MATERIALS AND METHODS: ADNP expression was assessed in peripheral blood mononuclear cells (PBMCs) from healthy donors and multiple sclerosis (MS) patients using staining with anti-ADNP (NAP) antibodies and markers for T cells, B cells, monocytes and natural killer cells. ADNP mRNA was determined in peripheral blood from MS patients (n = 24) and matched controls (n = 21). Expression of activation markers CD69 and CD154 and of IFN-γ was assessed by flow cytometry in stimulated PBMCs. Effects of NAP on immune cell proliferation was assessed by tritiated thymidine incorporation. RESULTS: Monocytes, B cells and T cells, but not regulatory (CD4+CD25+) T cells expressed ADNP. NAP peptide decreased the expression of CD69, CD154 and IFN-γ in PBMC and caused suppressed anti-CD3-/anti-CD28-stimulated PBMC proliferation. ADNP mRNA was reduced in MS compared to control peripheral blood. CONCLUSION: ADNP is expressed in many immune system cells. ADNP mRNA is reduced in PBMCs in MS. The peptide NAP, which plays an important role in neuroprotection, has potential immunomodulatory properties. S. Karger AG 2010-01 2009-11-17 /pmc/articles/PMC3701887/ /pubmed/19923857 http://dx.doi.org/10.1159/000258695 Text en Copyright © 2009 by S. Karger AG, Basel http://www.karger.com/Authors_Choice This is an open access article distributed under the terms of Karger's Author's Choice™ licensing agreement, adapted from the Creative Commons Attribution Non-Commercial 2.5 license. This license allows authors to re-use their articles for educational and research purposes as long as the author and the journal are fully acknowledged.
spellingShingle Original Paper
Braitch, Manjit
Kawabe, Kiyokazu
Nyirenda, Mukanthu
Gilles, Lucie Jean
Robins, R. Adrian
Gran, Bruno
Murphy, Sean
Showe, Louise
Constantinescu, Cris S.
Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title_full Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title_fullStr Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title_full_unstemmed Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title_short Expression of Activity-Dependent Neuroprotective Protein in the Immune System: Possible Functions and Relevance to Multiple Sclerosis
title_sort expression of activity-dependent neuroprotective protein in the immune system: possible functions and relevance to multiple sclerosis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701887/
https://www.ncbi.nlm.nih.gov/pubmed/19923857
http://dx.doi.org/10.1159/000258695
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