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Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines
Immortalized erythroid cell lines are expected to be a promising source of ex vivo manufactured red blood cells (RBCs), however the induction of enucleation in these cell lines is inefficient at present. We utilized an imaging-based high-throughput system to identify chemical compounds that trigger...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175573/ https://www.ncbi.nlm.nih.gov/pubmed/34083702 http://dx.doi.org/10.1038/s42003-021-02202-1 |
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author | Soboleva, Svetlana Kurita, Ryo Ek, Fredrik Åkerstrand, Hugo Silvério-Alves, Rita Olsson, Roger Nakamura, Yukio Miharada, Kenichi |
author_facet | Soboleva, Svetlana Kurita, Ryo Ek, Fredrik Åkerstrand, Hugo Silvério-Alves, Rita Olsson, Roger Nakamura, Yukio Miharada, Kenichi |
author_sort | Soboleva, Svetlana |
collection | PubMed |
description | Immortalized erythroid cell lines are expected to be a promising source of ex vivo manufactured red blood cells (RBCs), however the induction of enucleation in these cell lines is inefficient at present. We utilized an imaging-based high-throughput system to identify chemical compounds that trigger enucleation of human erythroid cell lines. Among >3,300 compounds, we identified multiple histone deacetylase inhibitors (HDACi) inducing enucleated cells from the cell line, although an increase in membrane fragility of enucleated cells was observed. Gene expression profiling revealed that HDACi treatment increased the expression of cytoskeletal genes, while an erythroid-specific cell membrane protein, SPTA1, was significantly down-regulated. Restoration of SPTA1 expression using CRISPR-activation partially rescued the fragility of cells and thereby improved the enucleation efficiency. Our observations provide a potential solution for the generation of mature cells from erythroid cell lines, contributing to the future realization of the use of immortalized cell lines for transfusion therapies. |
format | Online Article Text |
id | pubmed-8175573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81755732021-06-07 Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines Soboleva, Svetlana Kurita, Ryo Ek, Fredrik Åkerstrand, Hugo Silvério-Alves, Rita Olsson, Roger Nakamura, Yukio Miharada, Kenichi Commun Biol Article Immortalized erythroid cell lines are expected to be a promising source of ex vivo manufactured red blood cells (RBCs), however the induction of enucleation in these cell lines is inefficient at present. We utilized an imaging-based high-throughput system to identify chemical compounds that trigger enucleation of human erythroid cell lines. Among >3,300 compounds, we identified multiple histone deacetylase inhibitors (HDACi) inducing enucleated cells from the cell line, although an increase in membrane fragility of enucleated cells was observed. Gene expression profiling revealed that HDACi treatment increased the expression of cytoskeletal genes, while an erythroid-specific cell membrane protein, SPTA1, was significantly down-regulated. Restoration of SPTA1 expression using CRISPR-activation partially rescued the fragility of cells and thereby improved the enucleation efficiency. Our observations provide a potential solution for the generation of mature cells from erythroid cell lines, contributing to the future realization of the use of immortalized cell lines for transfusion therapies. Nature Publishing Group UK 2021-06-03 /pmc/articles/PMC8175573/ /pubmed/34083702 http://dx.doi.org/10.1038/s42003-021-02202-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Soboleva, Svetlana Kurita, Ryo Ek, Fredrik Åkerstrand, Hugo Silvério-Alves, Rita Olsson, Roger Nakamura, Yukio Miharada, Kenichi Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title | Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title_full | Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title_fullStr | Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title_full_unstemmed | Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title_short | Identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
title_sort | identification of potential chemical compounds enhancing generation of enucleated cells from immortalized human erythroid cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175573/ https://www.ncbi.nlm.nih.gov/pubmed/34083702 http://dx.doi.org/10.1038/s42003-021-02202-1 |
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