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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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 |
work_keys_str_mv |
AT joohyunryu aproteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells AT byoungchulpark aproteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells AT doheelee aproteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells AT joohyunryu proteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells AT byoungchulpark proteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells AT doheelee proteomicanalysisofdifferentiatingdopamineneuronsderivedfromhumanembryonicstemcells |
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