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Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis
Hematopoietic stem cells (HSCs) inhabit distinct microenvironments within the adult bone marrow (BM), which govern the delicate balance between HSC quiescence, self-renewal, and differentiation. Previous reports have proposed that HSCs localize to the vascular niche, comprised of endothelium and tig...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649106/ https://www.ncbi.nlm.nih.gov/pubmed/26441307 http://dx.doi.org/10.1016/j.stemcr.2015.08.018 |
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author | Poulos, Michael G. Crowley, Michael J.P. Gutkin, Michael C. Ramalingam, Pradeep Schachterle, William Thomas, Jean-Leon Elemento, Olivier Butler, Jason M. |
author_facet | Poulos, Michael G. Crowley, Michael J.P. Gutkin, Michael C. Ramalingam, Pradeep Schachterle, William Thomas, Jean-Leon Elemento, Olivier Butler, Jason M. |
author_sort | Poulos, Michael G. |
collection | PubMed |
description | Hematopoietic stem cells (HSCs) inhabit distinct microenvironments within the adult bone marrow (BM), which govern the delicate balance between HSC quiescence, self-renewal, and differentiation. Previous reports have proposed that HSCs localize to the vascular niche, comprised of endothelium and tightly associated perivascular cells. Herein, we examine the capacity of BM endothelial cells (BMECs) to support ex vivo and in vivo hematopoiesis. We demonstrate that AKT1-activated BMECs (BMEC-Akt1) have a unique transcription factor/cytokine profile that supports functional HSCs in lieu of complex serum and cytokine supplementation. Additionally, transplantation of BMEC-Akt1 cells enhanced regenerative hematopoiesis following myeloablative irradiation. These data demonstrate that BMEC-Akt1 cultures can be used as a platform for the discovery of pro-HSC factors and justify the utility of BMECs as a cellular therapy. This technical advance may lead to the development of therapies designed to decrease pancytopenias associated with myeloablative regimens used to treat a wide array of disease states. |
format | Online Article Text |
id | pubmed-4649106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-46491062015-12-11 Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis Poulos, Michael G. Crowley, Michael J.P. Gutkin, Michael C. Ramalingam, Pradeep Schachterle, William Thomas, Jean-Leon Elemento, Olivier Butler, Jason M. Stem Cell Reports Resource Hematopoietic stem cells (HSCs) inhabit distinct microenvironments within the adult bone marrow (BM), which govern the delicate balance between HSC quiescence, self-renewal, and differentiation. Previous reports have proposed that HSCs localize to the vascular niche, comprised of endothelium and tightly associated perivascular cells. Herein, we examine the capacity of BM endothelial cells (BMECs) to support ex vivo and in vivo hematopoiesis. We demonstrate that AKT1-activated BMECs (BMEC-Akt1) have a unique transcription factor/cytokine profile that supports functional HSCs in lieu of complex serum and cytokine supplementation. Additionally, transplantation of BMEC-Akt1 cells enhanced regenerative hematopoiesis following myeloablative irradiation. These data demonstrate that BMEC-Akt1 cultures can be used as a platform for the discovery of pro-HSC factors and justify the utility of BMECs as a cellular therapy. This technical advance may lead to the development of therapies designed to decrease pancytopenias associated with myeloablative regimens used to treat a wide array of disease states. Elsevier 2015-10-01 /pmc/articles/PMC4649106/ /pubmed/26441307 http://dx.doi.org/10.1016/j.stemcr.2015.08.018 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Resource Poulos, Michael G. Crowley, Michael J.P. Gutkin, Michael C. Ramalingam, Pradeep Schachterle, William Thomas, Jean-Leon Elemento, Olivier Butler, Jason M. Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title | Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title_full | Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title_fullStr | Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title_full_unstemmed | Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title_short | Vascular Platform to Define Hematopoietic Stem Cell Factors and Enhance Regenerative Hematopoiesis |
title_sort | vascular platform to define hematopoietic stem cell factors and enhance regenerative hematopoiesis |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649106/ https://www.ncbi.nlm.nih.gov/pubmed/26441307 http://dx.doi.org/10.1016/j.stemcr.2015.08.018 |
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