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Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children

Autism is one of the most common neurological developmental disorder associated with social isolation and restricted interests in children. The etiology of this disorder is still unknown. There is neither any confirmed laboratory test nor any effective therapeutic strategy to diagnose or cure it. To...

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Autores principales: Shen, Liming, Feng, Chengyun, Zhang, Kaoyuan, Chen, Youjiao, Gao, Yan, Ke, Junyan, Chen, Xinqian, Lin, Jing, Li, Cuihua, Iqbal, Javed, Zhao, Yuxi, Wang, Weibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433831/
https://www.ncbi.nlm.nih.gov/pubmed/30941018
http://dx.doi.org/10.3389/fncel.2019.00105
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author Shen, Liming
Feng, Chengyun
Zhang, Kaoyuan
Chen, Youjiao
Gao, Yan
Ke, Junyan
Chen, Xinqian
Lin, Jing
Li, Cuihua
Iqbal, Javed
Zhao, Yuxi
Wang, Weibin
author_facet Shen, Liming
Feng, Chengyun
Zhang, Kaoyuan
Chen, Youjiao
Gao, Yan
Ke, Junyan
Chen, Xinqian
Lin, Jing
Li, Cuihua
Iqbal, Javed
Zhao, Yuxi
Wang, Weibin
author_sort Shen, Liming
collection PubMed
description Autism is one of the most common neurological developmental disorder associated with social isolation and restricted interests in children. The etiology of this disorder is still unknown. There is neither any confirmed laboratory test nor any effective therapeutic strategy to diagnose or cure it. To search for biomarkers for early detection and exploration of the disease mechanisms, here, we investigated the protein expression signatures of peripheral blood mononuclear cells (PBMCs) in autistic children compared with healthy controls by using isobaric tags for relative and absolute quantitation (iTRAQ) proteomics approach. The results showed a total of 41 proteins as differentially expressed in autistic group as compared to control. These proteins are found associated with metabolic pathways, endoplasmic reticulum (ER) stress and protein folding, endocytosis, immune and inflammatory response, plasma lipoprotein particle organization, and cell adhesion. Among these, 17 proteins (13 up-regulated and four down-regulated) are found to be linked with mitochondria. Eight proteins including three already reported proteins in our previous studies were selected to be verified. Five already reported autism associated pro-inflammatory cytokines [interferon-γ (IFN-γ), interleukin-1β (IL-1β), IL-6, IL-12, and tumor necrosis factor-α (TNF-α)] were detected in plasma by enzyme-linked immunosorbent assay (ELISA) analysis. The results were consistent with proteomic results and reports from previous literature. These results proposed that PBMCs from autistic children might be activated, and ER stress, unfolded protein response (UPR), acute-phase response (APR), inflammatory response, and endocytosis may be involved in autism occurrence. These reported proteins may serve as potential biomarkers for early diagnosis of autism. More specifically, simultaneous detection of three proteins [complement C3 (C3), calreticulin (CALR), and SERPINA1] in the plasma and PBMCs could increase the authenticity of detection.
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spelling pubmed-64338312019-04-02 Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children Shen, Liming Feng, Chengyun Zhang, Kaoyuan Chen, Youjiao Gao, Yan Ke, Junyan Chen, Xinqian Lin, Jing Li, Cuihua Iqbal, Javed Zhao, Yuxi Wang, Weibin Front Cell Neurosci Neuroscience Autism is one of the most common neurological developmental disorder associated with social isolation and restricted interests in children. The etiology of this disorder is still unknown. There is neither any confirmed laboratory test nor any effective therapeutic strategy to diagnose or cure it. To search for biomarkers for early detection and exploration of the disease mechanisms, here, we investigated the protein expression signatures of peripheral blood mononuclear cells (PBMCs) in autistic children compared with healthy controls by using isobaric tags for relative and absolute quantitation (iTRAQ) proteomics approach. The results showed a total of 41 proteins as differentially expressed in autistic group as compared to control. These proteins are found associated with metabolic pathways, endoplasmic reticulum (ER) stress and protein folding, endocytosis, immune and inflammatory response, plasma lipoprotein particle organization, and cell adhesion. Among these, 17 proteins (13 up-regulated and four down-regulated) are found to be linked with mitochondria. Eight proteins including three already reported proteins in our previous studies were selected to be verified. Five already reported autism associated pro-inflammatory cytokines [interferon-γ (IFN-γ), interleukin-1β (IL-1β), IL-6, IL-12, and tumor necrosis factor-α (TNF-α)] were detected in plasma by enzyme-linked immunosorbent assay (ELISA) analysis. The results were consistent with proteomic results and reports from previous literature. These results proposed that PBMCs from autistic children might be activated, and ER stress, unfolded protein response (UPR), acute-phase response (APR), inflammatory response, and endocytosis may be involved in autism occurrence. These reported proteins may serve as potential biomarkers for early diagnosis of autism. More specifically, simultaneous detection of three proteins [complement C3 (C3), calreticulin (CALR), and SERPINA1] in the plasma and PBMCs could increase the authenticity of detection. Frontiers Media S.A. 2019-03-19 /pmc/articles/PMC6433831/ /pubmed/30941018 http://dx.doi.org/10.3389/fncel.2019.00105 Text en Copyright © 2019 Shen, Feng, Zhang, Chen, Gao, Ke, Chen, Lin, Li, Iqbal, Zhao and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shen, Liming
Feng, Chengyun
Zhang, Kaoyuan
Chen, Youjiao
Gao, Yan
Ke, Junyan
Chen, Xinqian
Lin, Jing
Li, Cuihua
Iqbal, Javed
Zhao, Yuxi
Wang, Weibin
Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title_full Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title_fullStr Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title_full_unstemmed Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title_short Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children
title_sort proteomics study of peripheral blood mononuclear cells (pbmcs) in autistic children
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433831/
https://www.ncbi.nlm.nih.gov/pubmed/30941018
http://dx.doi.org/10.3389/fncel.2019.00105
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