Department of Biochemistry and Molecular Biology, Biomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland; Department of Anatomy, Biomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Department of Anatomy, Biomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Mol Immunol. 2019 Jan;105:9-15. doi: 10.1016/j.molimm.2018.11.009. Epub 2018 Nov 22.
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 and Mitf, 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.
尽管已经描述了人类和犬类心脏中的肥大细胞分布,但小鼠心脏中的肥大细胞尚未被明确定位。因此,我们试图描述小鼠心脏中的肥大细胞分布,并研究其对小眼畸形相关转录因子(Mitf)的依赖性。使用甲苯胺蓝和亲和素染色来可视化肥大细胞,并描述其在心脏中的分布。心脏肥大细胞在心脏外膜(50%)或心肌(45%)中最为常见。较少见的是,在心内膜(5%)中也能观察到肥大细胞。在心肌中,31%的肥大细胞位于血管周围。通过研究两种不同的 Mitf 突变株,Mitf 和 Mitf,我们证明这些突变导致心脏肥大细胞几乎完全缺失。因此,mMCP-4 和 mMCP-5 基因的表达丢失,糜蛋白酶酶活性严重降低。此外,这些 Mitf 突变杂合子小鼠的心脏中肥大细胞数量明显少于野生型小鼠。我们的结果表明,小鼠心脏肥大细胞的分布与人类和犬类不同。心脏肥大细胞依赖于 Mitf 表达,Mitf 基因的功能丧失突变导致心脏肥大细胞几乎完全缺失。Mitf 基因的一个等位基因丢失足以导致相对肥大细胞缺乏。