A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells

Human embryonic stem cells (hESC) are being exploited for potential use in cell transplantation due to their capacity for self-renewal and pluripotency. Dopamine (DA) neurons derived from hESC represent a promising source of cell replacement therapy for Parkinson’s disease (PD). While gene expressio...

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Main Authors: Joohyun Ryu, Byoung Chul Park, Do Hee Lee
Format: Article
Language:English
Published: Taylor & Francis Group 2019-05-01
Series:Animal Cells and Systems
Subjects:
Online Access:http://dx.doi.org/10.1080/19768354.2019.1595140
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spelling doaj-55a690b3cc9b4ae98c2729a50f777fca2020-11-25T00:42:09ZengTaylor & Francis GroupAnimal Cells and Systems1976-83542151-24852019-05-0123321922710.1080/19768354.2019.15951401595140A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cellsJoohyun Ryu0Byoung Chul Park1Do Hee Lee2The Hormel Institute, University of MinnesotaKorea Research Institute of Bioscience and BiotechnologySeoul Women’s UniversityHuman embryonic stem cells (hESC) are being exploited for potential use in cell transplantation due to their capacity for self-renewal and pluripotency. Dopamine (DA) neurons derived from hESC represent a promising source of cell replacement therapy for Parkinson’s disease (PD). While gene expression on the transcriptome level has been extensively studied, limited information is available for the proteome-level changes associated with DA neuron differentiation. Here we analyzed the proteome of differentiating DA neurons to search for the potential biomarkers to assess the efficiency of differentiation. Although the proteome profile of DA neurons did not exhibit significant changes, a number of cytoskeletal proteins including nuclear lamin, tropomyosin 1, and myosin light chain 1 were specifically up-regulated during differentiation. Expression analysis of the respective genes was also consistent with the proteome results. In addition, these differentially expressed proteins form protein interaction network with several PD-related proteins suggesting that they may play roles in PD pathogenesis as well as the maturation of DA neurons.http://dx.doi.org/10.1080/19768354.2019.1595140Human embryonic stem cellsdopamine neuronproteomecytoskeletal proteins
collection DOAJ
language English
format Article
sources DOAJ
author Joohyun Ryu
Byoung Chul Park
Do Hee Lee
spellingShingle Joohyun Ryu
Byoung Chul Park
Do Hee Lee
A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
Animal Cells and Systems
Human embryonic stem cells
dopamine neuron
proteome
cytoskeletal proteins
author_facet Joohyun Ryu
Byoung Chul Park
Do Hee Lee
author_sort Joohyun Ryu
title A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
title_short A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
title_full A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
title_fullStr A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
title_full_unstemmed A proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
title_sort proteomic analysis of differentiating dopamine neurons derived from human embryonic stem cells
publisher Taylor & Francis Group
series Animal Cells and Systems
issn 1976-8354
2151-2485
publishDate 2019-05-01
description Human embryonic stem cells (hESC) are being exploited for potential use in cell transplantation due to their capacity for self-renewal and pluripotency. Dopamine (DA) neurons derived from hESC represent a promising source of cell replacement therapy for Parkinson’s disease (PD). While gene expression on the transcriptome level has been extensively studied, limited information is available for the proteome-level changes associated with DA neuron differentiation. Here we analyzed the proteome of differentiating DA neurons to search for the potential biomarkers to assess the efficiency of differentiation. Although the proteome profile of DA neurons did not exhibit significant changes, a number of cytoskeletal proteins including nuclear lamin, tropomyosin 1, and myosin light chain 1 were specifically up-regulated during differentiation. Expression analysis of the respective genes was also consistent with the proteome results. In addition, these differentially expressed proteins form protein interaction network with several PD-related proteins suggesting that they may play roles in PD pathogenesis as well as the maturation of DA neurons.
topic Human embryonic stem cells
dopamine neuron
proteome
cytoskeletal proteins
url http://dx.doi.org/10.1080/19768354.2019.1595140
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