Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells

Inflammation may play a role in cancer. However, the contribution of cytokine-mediated crosstalk between normal hemopoietic stem/progenitor cells (HSPCs) and their (inflammatory) microenvironment is largely elusive. Here we compared survival, phenotype, and function of neonatal (umbilical cord blood...

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Main Authors: Dorian Forte, Daria Sollazzo, Martina Barone, Marisole Allegri, Angela di Martella Orsi, Marco Romano, Barbara Sinigaglia, Giuseppe Auteri, Nicola Vianelli, Michele Cavo, Francesca Palandri, Lucia Catani
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2018/5974613
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author Dorian Forte
Daria Sollazzo
Martina Barone
Marisole Allegri
Angela di Martella Orsi
Marco Romano
Barbara Sinigaglia
Giuseppe Auteri
Nicola Vianelli
Michele Cavo
Francesca Palandri
Lucia Catani
author_facet Dorian Forte
Daria Sollazzo
Martina Barone
Marisole Allegri
Angela di Martella Orsi
Marco Romano
Barbara Sinigaglia
Giuseppe Auteri
Nicola Vianelli
Michele Cavo
Francesca Palandri
Lucia Catani
author_sort Dorian Forte
collection DOAJ
description Inflammation may play a role in cancer. However, the contribution of cytokine-mediated crosstalk between normal hemopoietic stem/progenitor cells (HSPCs) and their (inflammatory) microenvironment is largely elusive. Here we compared survival, phenotype, and function of neonatal (umbilical cord blood (CB)) and adult (normal G-CSF-mobilized peripheral blood (mPB)) CD34+ cells after in vitro exposure to combined crucial inflammatory factors such as interleukin- (IL-) 1β, IL-6, tumor necrosis factor- (TNF-) α, or tissue inhibitor of metalloproteinases-1 (TIMP-1). To mimic bone marrow (BM) niche, coculture experiments with normal BM stromal cells (BMSCs) were also performed. We found that combined inflammatory cytokines increased only the in vitro survival of CB-derived CD34+ cells by reducing apoptosis. Conversely, selected combinations of inflammatory cytokines (IL-1β + TNF-α, IL-6 + TNF-α, and IL-1β + TNF-α + TIMP-1) mainly enhanced the in vitro CXCR4-driven migration of mPB-derived CD34+ cells. TNF-α, alone or in combination, upregulated CD44 and CD13 expression in both sources. Finally, BMSCs alone increased survival/migration of CB- and mPB-derived CD34+ cells at the same extent of the combined inflammatory cytokines; importantly, their copresence did not show additive/synergistic effect. Taken together, these data indicate that combined proinflammatory stimuli promote distinct in vitro functional activation of neonatal or adult normal HSPCs.
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spelling doaj-art-572a768e4dbe4e188a3de7cac45d685a2025-08-20T02:05:57ZengWileyMediators of Inflammation0962-93511466-18612018-01-01201810.1155/2018/59746135974613Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ CellsDorian Forte0Daria Sollazzo1Martina Barone2Marisole Allegri3Angela di Martella Orsi4Marco Romano5Barbara Sinigaglia6Giuseppe Auteri7Nicola Vianelli8Michele Cavo9Francesca Palandri10Lucia Catani11Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalySchool of Immunology & Microbial Sciences, King’s College London, Guy’s Hospital, SE1 9RT London, UKDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, ItalyInflammation may play a role in cancer. However, the contribution of cytokine-mediated crosstalk between normal hemopoietic stem/progenitor cells (HSPCs) and their (inflammatory) microenvironment is largely elusive. Here we compared survival, phenotype, and function of neonatal (umbilical cord blood (CB)) and adult (normal G-CSF-mobilized peripheral blood (mPB)) CD34+ cells after in vitro exposure to combined crucial inflammatory factors such as interleukin- (IL-) 1β, IL-6, tumor necrosis factor- (TNF-) α, or tissue inhibitor of metalloproteinases-1 (TIMP-1). To mimic bone marrow (BM) niche, coculture experiments with normal BM stromal cells (BMSCs) were also performed. We found that combined inflammatory cytokines increased only the in vitro survival of CB-derived CD34+ cells by reducing apoptosis. Conversely, selected combinations of inflammatory cytokines (IL-1β + TNF-α, IL-6 + TNF-α, and IL-1β + TNF-α + TIMP-1) mainly enhanced the in vitro CXCR4-driven migration of mPB-derived CD34+ cells. TNF-α, alone or in combination, upregulated CD44 and CD13 expression in both sources. Finally, BMSCs alone increased survival/migration of CB- and mPB-derived CD34+ cells at the same extent of the combined inflammatory cytokines; importantly, their copresence did not show additive/synergistic effect. Taken together, these data indicate that combined proinflammatory stimuli promote distinct in vitro functional activation of neonatal or adult normal HSPCs.http://dx.doi.org/10.1155/2018/5974613
spellingShingle Dorian Forte
Daria Sollazzo
Martina Barone
Marisole Allegri
Angela di Martella Orsi
Marco Romano
Barbara Sinigaglia
Giuseppe Auteri
Nicola Vianelli
Michele Cavo
Francesca Palandri
Lucia Catani
Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
Mediators of Inflammation
title Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
title_full Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
title_fullStr Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
title_full_unstemmed Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
title_short Mobilized Peripheral Blood versus Cord Blood: Insight into the Distinct Role of Proinflammatory Cytokines on Survival, Clonogenic Ability, and Migration of CD34+ Cells
title_sort mobilized peripheral blood versus cord blood insight into the distinct role of proinflammatory cytokines on survival clonogenic ability and migration of cd34 cells
url http://dx.doi.org/10.1155/2018/5974613
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