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Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells

Mantle cell lymphoma (MCL) is associated with a significant risk of therapeutic failure and disease relapse, but the biological origin of relapse is poorly understood. Here, we prospectively identify subpopulations of primary MCL cells with different biologic and immunophenotypic features. Using a s...

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Autores principales: Medina, Daniel J., Abass-Shereef, Jeneba, Walton, Kelly, Goodell, Lauri, Aviv, Hana, Strair, Roger K., Budak-Alpdogan, Tulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982953/
https://www.ncbi.nlm.nih.gov/pubmed/24722054
http://dx.doi.org/10.1371/journal.pone.0091042
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author Medina, Daniel J.
Abass-Shereef, Jeneba
Walton, Kelly
Goodell, Lauri
Aviv, Hana
Strair, Roger K.
Budak-Alpdogan, Tulin
author_facet Medina, Daniel J.
Abass-Shereef, Jeneba
Walton, Kelly
Goodell, Lauri
Aviv, Hana
Strair, Roger K.
Budak-Alpdogan, Tulin
author_sort Medina, Daniel J.
collection PubMed
description Mantle cell lymphoma (MCL) is associated with a significant risk of therapeutic failure and disease relapse, but the biological origin of relapse is poorly understood. Here, we prospectively identify subpopulations of primary MCL cells with different biologic and immunophenotypic features. Using a simple culture system, we demonstrate that a subset of primary MCL cells co-cultured with either primary human mesenchymal stromal cells (hMSC) or murine MS-5 cells form in cobblestone-areas consisting of cells with a primitive immunophenotype (CD19−CD133+) containing the chromosomal translocation t (11;14)(q13;q32) characteristic of MCL. Limiting dilution serial transplantation experiments utilizing immunodeficient mice revealed that primary MCL engraftment was only observed when either unsorted or CD19−CD133+ cells were utilized. No engraftment was seen using the CD19+CD133− subpopulation. Our results establish that primary CD19−CD133+ MCL cells are a functionally distinct subpopulation of primary MCL cells enriched for MCL-initiating activity in immunodeficient mice. This rare subpopulation of MCL-initiating cells may play an important role in the pathogenesis of MCL.
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spelling pubmed-39829532014-04-15 Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells Medina, Daniel J. Abass-Shereef, Jeneba Walton, Kelly Goodell, Lauri Aviv, Hana Strair, Roger K. Budak-Alpdogan, Tulin PLoS One Research Article Mantle cell lymphoma (MCL) is associated with a significant risk of therapeutic failure and disease relapse, but the biological origin of relapse is poorly understood. Here, we prospectively identify subpopulations of primary MCL cells with different biologic and immunophenotypic features. Using a simple culture system, we demonstrate that a subset of primary MCL cells co-cultured with either primary human mesenchymal stromal cells (hMSC) or murine MS-5 cells form in cobblestone-areas consisting of cells with a primitive immunophenotype (CD19−CD133+) containing the chromosomal translocation t (11;14)(q13;q32) characteristic of MCL. Limiting dilution serial transplantation experiments utilizing immunodeficient mice revealed that primary MCL engraftment was only observed when either unsorted or CD19−CD133+ cells were utilized. No engraftment was seen using the CD19+CD133− subpopulation. Our results establish that primary CD19−CD133+ MCL cells are a functionally distinct subpopulation of primary MCL cells enriched for MCL-initiating activity in immunodeficient mice. This rare subpopulation of MCL-initiating cells may play an important role in the pathogenesis of MCL. Public Library of Science 2014-04-10 /pmc/articles/PMC3982953/ /pubmed/24722054 http://dx.doi.org/10.1371/journal.pone.0091042 Text en © 2014 Medina et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Medina, Daniel J.
Abass-Shereef, Jeneba
Walton, Kelly
Goodell, Lauri
Aviv, Hana
Strair, Roger K.
Budak-Alpdogan, Tulin
Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title_full Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title_fullStr Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title_full_unstemmed Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title_short Cobblestone-Area Forming Cells Derived from Patients with Mantle Cell Lymphoma Are Enriched for CD133(+) Tumor-Initiating Cells
title_sort cobblestone-area forming cells derived from patients with mantle cell lymphoma are enriched for cd133(+) tumor-initiating cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982953/
https://www.ncbi.nlm.nih.gov/pubmed/24722054
http://dx.doi.org/10.1371/journal.pone.0091042
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