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Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation

Cell therapies represent a promising approach to slow down the progression of currently untreatable neurodegenerative diseases (e.g., Alzheimer's and Parkinson's disease or amyotrophic lateral sclerosis), as well as to support the reconstruction of functional neural circuits after spinal c...

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Autores principales: Červenka, Jakub, Tylečková, Jiřina, Kupcová Skalníková, Helena, Vodičková Kepková, Kateřina, Poliakh, Ievgeniia, Valeková, Ivona, Pfeiferová, Lucie, Kolář, Michal, Vaškovičová, Michaela, Pánková, Tereza, Vodička, Petr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876319/
https://www.ncbi.nlm.nih.gov/pubmed/33584205
http://dx.doi.org/10.3389/fncel.2020.612560
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author Červenka, Jakub
Tylečková, Jiřina
Kupcová Skalníková, Helena
Vodičková Kepková, Kateřina
Poliakh, Ievgeniia
Valeková, Ivona
Pfeiferová, Lucie
Kolář, Michal
Vaškovičová, Michaela
Pánková, Tereza
Vodička, Petr
author_facet Červenka, Jakub
Tylečková, Jiřina
Kupcová Skalníková, Helena
Vodičková Kepková, Kateřina
Poliakh, Ievgeniia
Valeková, Ivona
Pfeiferová, Lucie
Kolář, Michal
Vaškovičová, Michaela
Pánková, Tereza
Vodička, Petr
author_sort Červenka, Jakub
collection PubMed
description Cell therapies represent a promising approach to slow down the progression of currently untreatable neurodegenerative diseases (e.g., Alzheimer's and Parkinson's disease or amyotrophic lateral sclerosis), as well as to support the reconstruction of functional neural circuits after spinal cord injuries. In such therapies, the grafted cells could either functionally integrate into the damaged tissue, partially replacing dead or damaged cells, modulate inflammatory reaction, reduce tissue damage, or support neuronal survival by secretion of cytokines, growth, and trophic factors. Comprehensive characterization of cells and their proliferative potential, differentiation status, and population purity before transplantation is crucial to preventing safety risks, e.g., a tumorous growth due to the proliferation of undifferentiated stem cells. We characterized changes in the proteome and secretome of human neural stem cells (NSCs) during their spontaneous (EGF/FGF2 withdrawal) differentiation and differentiation with trophic support by BDNF/GDNF supplementation. We used LC-MS/MS in SWATH-MS mode for global cellular proteome profiling and quantified almost three thousand cellular proteins. Our analysis identified substantial protein differences in the early stages of NSC differentiation with more than a third of all the proteins regulated (including known neuronal and NSC multipotency markers) and revealed that the BDNF/GDNF support affected more the later stages of the NSC differentiation. Among the pathways identified as activated during both spontaneous and BDNF/GDNF differentiation were the HIF-1 signaling pathway, Wnt signaling pathway, and VEGF signaling pathway. Our follow-up secretome analysis using Luminex multiplex immunoassay revealed significant changes in the secretion of VEGF and IL-6 during NSC differentiation. Our results further demonstrated an increased expression of neuropilin-1 as well as catenin β-1, both known to participate in the regulation of VEGF signaling, and showed that VEGF-A isoform 121 (VEGF121), in particular, induces proliferation and supports survival of differentiating cells.
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spelling pubmed-78763192021-02-12 Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation Červenka, Jakub Tylečková, Jiřina Kupcová Skalníková, Helena Vodičková Kepková, Kateřina Poliakh, Ievgeniia Valeková, Ivona Pfeiferová, Lucie Kolář, Michal Vaškovičová, Michaela Pánková, Tereza Vodička, Petr Front Cell Neurosci Cellular Neuroscience Cell therapies represent a promising approach to slow down the progression of currently untreatable neurodegenerative diseases (e.g., Alzheimer's and Parkinson's disease or amyotrophic lateral sclerosis), as well as to support the reconstruction of functional neural circuits after spinal cord injuries. In such therapies, the grafted cells could either functionally integrate into the damaged tissue, partially replacing dead or damaged cells, modulate inflammatory reaction, reduce tissue damage, or support neuronal survival by secretion of cytokines, growth, and trophic factors. Comprehensive characterization of cells and their proliferative potential, differentiation status, and population purity before transplantation is crucial to preventing safety risks, e.g., a tumorous growth due to the proliferation of undifferentiated stem cells. We characterized changes in the proteome and secretome of human neural stem cells (NSCs) during their spontaneous (EGF/FGF2 withdrawal) differentiation and differentiation with trophic support by BDNF/GDNF supplementation. We used LC-MS/MS in SWATH-MS mode for global cellular proteome profiling and quantified almost three thousand cellular proteins. Our analysis identified substantial protein differences in the early stages of NSC differentiation with more than a third of all the proteins regulated (including known neuronal and NSC multipotency markers) and revealed that the BDNF/GDNF support affected more the later stages of the NSC differentiation. Among the pathways identified as activated during both spontaneous and BDNF/GDNF differentiation were the HIF-1 signaling pathway, Wnt signaling pathway, and VEGF signaling pathway. Our follow-up secretome analysis using Luminex multiplex immunoassay revealed significant changes in the secretion of VEGF and IL-6 during NSC differentiation. Our results further demonstrated an increased expression of neuropilin-1 as well as catenin β-1, both known to participate in the regulation of VEGF signaling, and showed that VEGF-A isoform 121 (VEGF121), in particular, induces proliferation and supports survival of differentiating cells. Frontiers Media S.A. 2021-01-28 /pmc/articles/PMC7876319/ /pubmed/33584205 http://dx.doi.org/10.3389/fncel.2020.612560 Text en Copyright © 2021 Červenka, Tylečková, Kupcová Skalníková, Vodičková Kepková, Poliakh, Valeková, Pfeiferová, Kolář, Vaškovičová, Pánková and Vodička. 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 Cellular Neuroscience
Červenka, Jakub
Tylečková, Jiřina
Kupcová Skalníková, Helena
Vodičková Kepková, Kateřina
Poliakh, Ievgeniia
Valeková, Ivona
Pfeiferová, Lucie
Kolář, Michal
Vaškovičová, Michaela
Pánková, Tereza
Vodička, Petr
Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title_full Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title_fullStr Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title_full_unstemmed Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title_short Proteomic Characterization of Human Neural Stem Cells and Their Secretome During in vitro Differentiation
title_sort proteomic characterization of human neural stem cells and their secretome during in vitro differentiation
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876319/
https://www.ncbi.nlm.nih.gov/pubmed/33584205
http://dx.doi.org/10.3389/fncel.2020.612560
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