Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions

Mast cells (MCs) are long-living multifunctional innate immune cells that originate from hematopoietic precursors and specifically differentiate in the destination tissue, e.g., skin, respiratory mucosa, intestine, where they mediate immune cell recruitment and antimicrobial defense. In vivo these t...

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Main Authors: Helene Möllerherm, Karsten Meier, Kathrin Schmies, Herbert Fuhrmann, Hassan Y. Naim, Maren von Köckritz-Blickwede, Katja Branitzki-Heinemann
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.01665/full
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spelling doaj-8d85280fd8bc4e86bb446e5c5b8d0ec72020-11-24T21:43:15ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-11-01810.3389/fimmu.2017.01665305500Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen ConditionsHelene Möllerherm0Karsten Meier1Kathrin Schmies2Herbert Fuhrmann3Hassan Y. Naim4Maren von Köckritz-Blickwede5Maren von Köckritz-Blickwede6Katja Branitzki-Heinemann7Department of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyDepartment of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyDepartment of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyFaculty of Veterinary Medicine, Institute of Biochemistry, University of Leipzig, Leipzig, GermanyDepartment of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyDepartment of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyResearch Center for Emerging Infections and Zoonoses (RIZ), University for Veterinary Medicine Hannover, Hanover, GermanyDepartment of Physiological Chemistry, University for Veterinary Medicine Hannover, Hanover, GermanyMast cells (MCs) are long-living multifunctional innate immune cells that originate from hematopoietic precursors and specifically differentiate in the destination tissue, e.g., skin, respiratory mucosa, intestine, where they mediate immune cell recruitment and antimicrobial defense. In vivo these tissues have characteristic physiological oxygen levels that are considerably lower than the atmospheric oxygen conditions (159 mmHg, 21% O2; 5% CO2) traditionally used to differentiate MCs and to study their functionality in vitro. Only little is known about the impact of physiological oxygen conditions on the differentiation process of MCs. This study aimed to characterize the differentiation of immature murine bone marrow-derived MCs under physioxia in vitro (7% O2; 53 mmHg; 5% CO2). Bone marrow-derived suspension cells were differentiated in the presence of interleukin-3 with continuous, non-invasive determination of the oxygen level using a Fibox4-PSt3 measurement system without technique-caused oxygen consumption. Trypan blue staining confirmed cellular viability during the specified period. Interestingly, MCs cultivated at 7% O2 showed a significantly delayed differentiation rate defined by CD117-positive cells, analyzed by flow cytometry, and reached >95% CD117 positive population at day 32 after isolation. Importantly, MCs differentiated under physioxia displayed a decreased transcript expression level of hif-1α and selected target genes vegf, il-6, and tnf-α, but an increase of foxo3 and vhl expression compared to MCs cultivated under normoxia. Moreover, the production of reactive oxygen species as well as the amount of intracellular stored histamine was significantly lower in MCs differentiated under low oxygen levels, which might have consequences for their function such as immunomodulation of other immune cells. These results show for the first time that physioxia substantially affect maturation and the properties of MCs and highlight the need to study their function under physiologically relevant oxygen conditions.http://journal.frontiersin.org/article/10.3389/fimmu.2017.01665/fullmast cellsphysioxiaHIF-1αFOXO3histaminereactive oxygen species
collection DOAJ
language English
format Article
sources DOAJ
author Helene Möllerherm
Karsten Meier
Kathrin Schmies
Herbert Fuhrmann
Hassan Y. Naim
Maren von Köckritz-Blickwede
Maren von Köckritz-Blickwede
Katja Branitzki-Heinemann
spellingShingle Helene Möllerherm
Karsten Meier
Kathrin Schmies
Herbert Fuhrmann
Hassan Y. Naim
Maren von Köckritz-Blickwede
Maren von Köckritz-Blickwede
Katja Branitzki-Heinemann
Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
Frontiers in Immunology
mast cells
physioxia
HIF-1α
FOXO3
histamine
reactive oxygen species
author_facet Helene Möllerherm
Karsten Meier
Kathrin Schmies
Herbert Fuhrmann
Hassan Y. Naim
Maren von Köckritz-Blickwede
Maren von Köckritz-Blickwede
Katja Branitzki-Heinemann
author_sort Helene Möllerherm
title Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
title_short Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
title_full Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
title_fullStr Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
title_full_unstemmed Differentiation and Functionality of Bone Marrow-Derived Mast Cells Depend on Varying Physiologic Oxygen Conditions
title_sort differentiation and functionality of bone marrow-derived mast cells depend on varying physiologic oxygen conditions
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2017-11-01
description Mast cells (MCs) are long-living multifunctional innate immune cells that originate from hematopoietic precursors and specifically differentiate in the destination tissue, e.g., skin, respiratory mucosa, intestine, where they mediate immune cell recruitment and antimicrobial defense. In vivo these tissues have characteristic physiological oxygen levels that are considerably lower than the atmospheric oxygen conditions (159 mmHg, 21% O2; 5% CO2) traditionally used to differentiate MCs and to study their functionality in vitro. Only little is known about the impact of physiological oxygen conditions on the differentiation process of MCs. This study aimed to characterize the differentiation of immature murine bone marrow-derived MCs under physioxia in vitro (7% O2; 53 mmHg; 5% CO2). Bone marrow-derived suspension cells were differentiated in the presence of interleukin-3 with continuous, non-invasive determination of the oxygen level using a Fibox4-PSt3 measurement system without technique-caused oxygen consumption. Trypan blue staining confirmed cellular viability during the specified period. Interestingly, MCs cultivated at 7% O2 showed a significantly delayed differentiation rate defined by CD117-positive cells, analyzed by flow cytometry, and reached >95% CD117 positive population at day 32 after isolation. Importantly, MCs differentiated under physioxia displayed a decreased transcript expression level of hif-1α and selected target genes vegf, il-6, and tnf-α, but an increase of foxo3 and vhl expression compared to MCs cultivated under normoxia. Moreover, the production of reactive oxygen species as well as the amount of intracellular stored histamine was significantly lower in MCs differentiated under low oxygen levels, which might have consequences for their function such as immunomodulation of other immune cells. These results show for the first time that physioxia substantially affect maturation and the properties of MCs and highlight the need to study their function under physiologically relevant oxygen conditions.
topic mast cells
physioxia
HIF-1α
FOXO3
histamine
reactive oxygen species
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.01665/full
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