How “Neuronal” Are Human Skin Mast Cells?

Mast cells are evolutionarily old cells and the principal effectors in allergic responses and inflammation. They are seeded from the yolk sac during embryogenesis or are derived from hematopoietic progenitors and are therefore related to other leukocyte subsets, even though they form a separate clad...

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Main Authors: Magda Babina, Kristin Franke, Gürkan Bal
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/18/10871
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author Magda Babina
Kristin Franke
Gürkan Bal
author_facet Magda Babina
Kristin Franke
Gürkan Bal
author_sort Magda Babina
collection DOAJ
description Mast cells are evolutionarily old cells and the principal effectors in allergic responses and inflammation. They are seeded from the yolk sac during embryogenesis or are derived from hematopoietic progenitors and are therefore related to other leukocyte subsets, even though they form a separate clade in the hematopoietic system. Herein, we systematically bundle information from several recent high-throughput endeavors, especially those comparing MCs with other cell types, and combine such information with knowledge on the genes’ functions to reveal groups of neuronal markers specifically expressed by MCs. We focus on recent advances made regarding human tissue MCs, but also refer to studies in mice. In broad terms, genes hyper-expressed in MCs, but largely inactive in other myelocytes, can be classified into subcategories such as traffic/lysosomes (MLPH and RAB27B), the dopamine system (MAOB, DRD2, SLC6A3, and SLC18A2), Ca<sup>2+</sup>-related entities (CALB2), adhesion molecules (L1CAM and NTM) and, as an overall principle, the transcription factors and modulators of transcriptional activity (LMO4, PBX1, MEIS2, and EHMT2). Their function in MCs is generally unknown but may tentatively be deduced by comparison with other systems. MCs share functions with the nervous system, as they express typical neurotransmitters (histamine and serotonin) and a degranulation machinery that shares features with the neuronal apparatus at the synapse. Therefore, selective overlaps are plausible, and they further highlight the uniqueness of MCs within the myeloid system, as well as when compared with basophils. Apart from investigating their functional implications in MCs, a key question is whether their expression in the lineage is due to the specific reactivation of genes normally silenced in leukocytes or whether the genes are not switched off during mastocytic development from early progenitors.
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spelling doaj.art-cbfbb1dea5894fbdaca0ea8c5a72832a2023-11-23T16:49:50ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-09-0123181087110.3390/ijms231810871How “Neuronal” Are Human Skin Mast Cells?Magda Babina0Kristin Franke1Gürkan Bal2Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology IA, 12203 Berlin, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology IA, 12203 Berlin, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology IA, 12203 Berlin, GermanyMast cells are evolutionarily old cells and the principal effectors in allergic responses and inflammation. They are seeded from the yolk sac during embryogenesis or are derived from hematopoietic progenitors and are therefore related to other leukocyte subsets, even though they form a separate clade in the hematopoietic system. Herein, we systematically bundle information from several recent high-throughput endeavors, especially those comparing MCs with other cell types, and combine such information with knowledge on the genes’ functions to reveal groups of neuronal markers specifically expressed by MCs. We focus on recent advances made regarding human tissue MCs, but also refer to studies in mice. In broad terms, genes hyper-expressed in MCs, but largely inactive in other myelocytes, can be classified into subcategories such as traffic/lysosomes (MLPH and RAB27B), the dopamine system (MAOB, DRD2, SLC6A3, and SLC18A2), Ca<sup>2+</sup>-related entities (CALB2), adhesion molecules (L1CAM and NTM) and, as an overall principle, the transcription factors and modulators of transcriptional activity (LMO4, PBX1, MEIS2, and EHMT2). Their function in MCs is generally unknown but may tentatively be deduced by comparison with other systems. MCs share functions with the nervous system, as they express typical neurotransmitters (histamine and serotonin) and a degranulation machinery that shares features with the neuronal apparatus at the synapse. Therefore, selective overlaps are plausible, and they further highlight the uniqueness of MCs within the myeloid system, as well as when compared with basophils. Apart from investigating their functional implications in MCs, a key question is whether their expression in the lineage is due to the specific reactivation of genes normally silenced in leukocytes or whether the genes are not switched off during mastocytic development from early progenitors.https://www.mdpi.com/1422-0067/23/18/10871mast cellsneuronsdegranulationdopamineadhesion moleculessolute carriers
spellingShingle Magda Babina
Kristin Franke
Gürkan Bal
How “Neuronal” Are Human Skin Mast Cells?
International Journal of Molecular Sciences
mast cells
neurons
degranulation
dopamine
adhesion molecules
solute carriers
title How “Neuronal” Are Human Skin Mast Cells?
title_full How “Neuronal” Are Human Skin Mast Cells?
title_fullStr How “Neuronal” Are Human Skin Mast Cells?
title_full_unstemmed How “Neuronal” Are Human Skin Mast Cells?
title_short How “Neuronal” Are Human Skin Mast Cells?
title_sort how neuronal are human skin mast cells
topic mast cells
neurons
degranulation
dopamine
adhesion molecules
solute carriers
url https://www.mdpi.com/1422-0067/23/18/10871
work_keys_str_mv AT magdababina howneuronalarehumanskinmastcells
AT kristinfranke howneuronalarehumanskinmastcells
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