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Distribution of mast cells within the mouse heart and its dependency on Mitf

Distribution of mast cells within the mouse heart and its dependency on Mitf


Titill: Distribution of mast cells within the mouse heart and its dependency on Mitf
Höfundur: Ingason, Arnar   orcid.org/0000-0003-0943-2523
Mechmet, Fatich   orcid.org/0000-0003-0596-0185
Atacho, Diahann   orcid.org/0000-0002-6158-0235
Steingrimsson, Eirikur   orcid.org/0000-0001-5826-7486
Petersen, Petur Henry   orcid.org/0000-0001-6622-3002
Útgáfa: 2019-01
Tungumál: Enska
Umfang: 9-15
Háskóli/Stofnun: Háskóli Íslands
University of Iceland
Svið: Heilbrigðisvísindasvið (HÍ)
School of Health Sciences (UI)
Deild: Læknadeild (HÍ)
Faculty of Medicine (UI)
Lífvísindasetur (HÍ)
Biomedical Center (UI)
Birtist í: Molecular Immunology;105
ISSN: 0161-5890
DOI: 10.1016/j.molimm.2018.11.009
Efnisorð: Chymase; Heart; Mast cells; Mice; Microphthalmia-associated transcription factor; Hjartað; Genarannsóknir; MITF
URI: https://hdl.handle.net/20.500.11815/2121

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Tilvitnun:

Ingason, A., Mechmet, F., Atacho, D., Steingrímsson, E., & Petersen, P. (2019). Distribution of mast cells within the mouse heart and its dependency on Mitf. Molecular Immunology, 105, 9-15.

Útdráttur:

Although mast cell distribution has been described in both human and canine hearts, cardiac mast cells in mice have yet to be categorically localized. We therefore sought to describe mast cell distribution within the mouse heart and characterize their dependence on the Microphthalmia-associated transcription factor (Mitf). Cardiac mast cells were visualized using Toluidine Blue and avidin staining, and their distribution within the heart described. Cardiac mast cells were most prevalent in the epicardium (50%) or myocardium (45%). Less frequently, mast cells were noted in the endocardium (5%). Within the myocardium, 31% of the mast cells had perivascular location. By studying two different Mitf mutant strains, Mitf mi−vga9 and Mitf Mi-wh , we demonstrated that these mutations led to near-complete deficiency of cardiac mast cells. Accordingly, expression of the mMCP-4 and mMCP-5 genes was lost and chymase enzyme activity was severely reduced. Additionally, hearts from mice heterozygous for these Mitf mutations contained significantly fewer mast cells compared to wild-type mice. Our results demonstrated that the distribution of cardiac mast cells in mice is different from humans and dogs. Cardiac mast cells are dependent on Mitf expression, with loss-of-function mutation in the Mitf gene leading to near-complete lack of cardiac mast cells. Loss of a single Mitf allele is sufficient for relative mast cell deficiency.

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This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/).T

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