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A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL

The presence, within the human bone marrow, of cells with both endothelial and hemogenic potential has been controversial. Herein, we identify, within the human fetal bone marrow, prior to establishment of hematopoiesis, a unique APLNR+, Stro-1+ cell population, coexpressing markers of early mesoder...

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Autores principales: Mokhtari, Saloomeh, Colletti, Evan, Yin, Weihong, Sanada, Chad, Lamar, Zanetta, Simmons, Paul J., Walker, Steven, Bishop, Colin, Atala, Anthony, Zanjani, Esmail D., Porada, Christopher D., Almeida-Porada, Graça
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035774/
https://www.ncbi.nlm.nih.gov/pubmed/29467489
http://dx.doi.org/10.1038/s41375-018-0016-1
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author Mokhtari, Saloomeh
Colletti, Evan
Yin, Weihong
Sanada, Chad
Lamar, Zanetta
Simmons, Paul J.
Walker, Steven
Bishop, Colin
Atala, Anthony
Zanjani, Esmail D.
Porada, Christopher D.
Almeida-Porada, Graça
author_facet Mokhtari, Saloomeh
Colletti, Evan
Yin, Weihong
Sanada, Chad
Lamar, Zanetta
Simmons, Paul J.
Walker, Steven
Bishop, Colin
Atala, Anthony
Zanjani, Esmail D.
Porada, Christopher D.
Almeida-Porada, Graça
author_sort Mokhtari, Saloomeh
collection PubMed
description The presence, within the human bone marrow, of cells with both endothelial and hemogenic potential has been controversial. Herein, we identify, within the human fetal bone marrow, prior to establishment of hematopoiesis, a unique APLNR+, Stro-1+ cell population, coexpressing markers of early mesodermal precursors and/or hemogenic endothelium. In adult marrow, cells expressing similar markers are also found, but at very low frequency. These adult-derived cells can be extensively culture expanded in vitro without loss of potential, they preserve a biased hemogenic transcriptional profile, and, upon in vitro induction with OCT4, assume a hematopoietic phenotype. In vivo, these cells, upon transplantation into a fetal microenvironment, contribute to the vasculature, and generate hematopoietic cells that provide multilineage repopulation upon serial transplantation. The identification of this human somatic cell population provides novel insights into human ontogenetic hematovascular potential, which could lead to a better understanding of, and new target therapies for, malignant and nonmalignant hematologic disorders.
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spelling pubmed-60357742018-08-02 A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL Mokhtari, Saloomeh Colletti, Evan Yin, Weihong Sanada, Chad Lamar, Zanetta Simmons, Paul J. Walker, Steven Bishop, Colin Atala, Anthony Zanjani, Esmail D. Porada, Christopher D. Almeida-Porada, Graça Leukemia Article The presence, within the human bone marrow, of cells with both endothelial and hemogenic potential has been controversial. Herein, we identify, within the human fetal bone marrow, prior to establishment of hematopoiesis, a unique APLNR+, Stro-1+ cell population, coexpressing markers of early mesodermal precursors and/or hemogenic endothelium. In adult marrow, cells expressing similar markers are also found, but at very low frequency. These adult-derived cells can be extensively culture expanded in vitro without loss of potential, they preserve a biased hemogenic transcriptional profile, and, upon in vitro induction with OCT4, assume a hematopoietic phenotype. In vivo, these cells, upon transplantation into a fetal microenvironment, contribute to the vasculature, and generate hematopoietic cells that provide multilineage repopulation upon serial transplantation. The identification of this human somatic cell population provides novel insights into human ontogenetic hematovascular potential, which could lead to a better understanding of, and new target therapies for, malignant and nonmalignant hematologic disorders. 2018-02-02 2018-07 /pmc/articles/PMC6035774/ /pubmed/29467489 http://dx.doi.org/10.1038/s41375-018-0016-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Mokhtari, Saloomeh
Colletti, Evan
Yin, Weihong
Sanada, Chad
Lamar, Zanetta
Simmons, Paul J.
Walker, Steven
Bishop, Colin
Atala, Anthony
Zanjani, Esmail D.
Porada, Christopher D.
Almeida-Porada, Graça
A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title_full A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title_fullStr A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title_full_unstemmed A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title_short A HUMAN BONE MARROW MESODERMAL-DERIVED CELL POPULATION WITH HEMOGENIC POTENTIAL
title_sort human bone marrow mesodermal-derived cell population with hemogenic potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035774/
https://www.ncbi.nlm.nih.gov/pubmed/29467489
http://dx.doi.org/10.1038/s41375-018-0016-1
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