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The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells
Pigment epithelium derived factor (PEDF), a ubiquitously expressed 50 kDa secreted glycoprotein, was recently discovered to regulate self-renewal of neural stem cells and have a supportive effect on human embryonic stem cell growth. Here, we analyzed expression of PEDF in the murine hematopoietic st...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579195/ https://www.ncbi.nlm.nih.gov/pubmed/28860613 http://dx.doi.org/10.1038/s41598-017-09452-2 |
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author | Rörby, Emma Billing, Matilda Dahl, Maria Warsi, Sarah Andradottir, Silja Miharada, Kenichi Siva, Kavitha Jönsson, Jan-Ingvar Blank, Ulrika Karlsson, Göran Karlsson, Stefan |
author_facet | Rörby, Emma Billing, Matilda Dahl, Maria Warsi, Sarah Andradottir, Silja Miharada, Kenichi Siva, Kavitha Jönsson, Jan-Ingvar Blank, Ulrika Karlsson, Göran Karlsson, Stefan |
author_sort | Rörby, Emma |
collection | PubMed |
description | Pigment epithelium derived factor (PEDF), a ubiquitously expressed 50 kDa secreted glycoprotein, was recently discovered to regulate self-renewal of neural stem cells and have a supportive effect on human embryonic stem cell growth. Here, we analyzed expression of PEDF in the murine hematopoietic stem cell (HSC) compartments and found that PEDF is highly expressed in primary long-term HSCs. Therefore, we characterized the hematopoietic system in a knockout mouse model for PEDF and using this model we surprisingly found that PEDF is dispensable for HSC regulation. PEDF knockout mice exhibit normal hematopoiesis in steady state conditions and the absence of PEDF lead to normal regeneration capacity in a serial competitive transplantation setting. Additionally, PEDF-deficient cells exhibit unaltered lineage distribution upon serial transplantations. When human cord blood stem and progenitor cells were cultured in media supplemented with recombinant PEDF they did not show changes in growth potential. Taken together, we report that PEDF is not a critical regulatory factor for HSC function during regeneration in vivo or growth of human stem/progenitor cells in vitro. |
format | Online Article Text |
id | pubmed-5579195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55791952017-09-06 The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells Rörby, Emma Billing, Matilda Dahl, Maria Warsi, Sarah Andradottir, Silja Miharada, Kenichi Siva, Kavitha Jönsson, Jan-Ingvar Blank, Ulrika Karlsson, Göran Karlsson, Stefan Sci Rep Article Pigment epithelium derived factor (PEDF), a ubiquitously expressed 50 kDa secreted glycoprotein, was recently discovered to regulate self-renewal of neural stem cells and have a supportive effect on human embryonic stem cell growth. Here, we analyzed expression of PEDF in the murine hematopoietic stem cell (HSC) compartments and found that PEDF is highly expressed in primary long-term HSCs. Therefore, we characterized the hematopoietic system in a knockout mouse model for PEDF and using this model we surprisingly found that PEDF is dispensable for HSC regulation. PEDF knockout mice exhibit normal hematopoiesis in steady state conditions and the absence of PEDF lead to normal regeneration capacity in a serial competitive transplantation setting. Additionally, PEDF-deficient cells exhibit unaltered lineage distribution upon serial transplantations. When human cord blood stem and progenitor cells were cultured in media supplemented with recombinant PEDF they did not show changes in growth potential. Taken together, we report that PEDF is not a critical regulatory factor for HSC function during regeneration in vivo or growth of human stem/progenitor cells in vitro. Nature Publishing Group UK 2017-08-31 /pmc/articles/PMC5579195/ /pubmed/28860613 http://dx.doi.org/10.1038/s41598-017-09452-2 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Rörby, Emma Billing, Matilda Dahl, Maria Warsi, Sarah Andradottir, Silja Miharada, Kenichi Siva, Kavitha Jönsson, Jan-Ingvar Blank, Ulrika Karlsson, Göran Karlsson, Stefan The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title | The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title_full | The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title_fullStr | The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title_full_unstemmed | The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title_short | The stem cell regulator PEDF is dispensable for maintenance and function of hematopoietic stem cells |
title_sort | stem cell regulator pedf is dispensable for maintenance and function of hematopoietic stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579195/ https://www.ncbi.nlm.nih.gov/pubmed/28860613 http://dx.doi.org/10.1038/s41598-017-09452-2 |
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