Mast Cell Tryptase and Carboxypeptidase A3 in the Formation of Ovarian Endometrioid Cysts

被引:7
作者
Atiakshin, Dmitri [1 ,2 ]
Patsap, Olga [1 ]
Kostin, Andrey [1 ]
Mikhalyova, Lyudmila [3 ]
Buchwalow, Igor [1 ,4 ]
Tiemann, Markus [4 ]
机构
[1] Peoples Friendship Univ Russia, Res & Educ Resource Ctr Immunophenotyping Digital, Moscow 117198, Russia
[2] Burdenko Voronezh State Med Univ, Res Inst Expt Biol & Med, Voronezh 394036, Russia
[3] Avtsyn Res Inst Human Morphol, Moscow 117418, Russia
[4] Inst Hematopathol, D-22547 Hamburg, Germany
关键词
tryptase; carboxypeptidase A3; mast cells; ovarian endometrioma; specific tissue microenvironment; INFLAMMATION; PROTEASES; PALMITOYLETHANOLAMIDE; INCREASE; TARGETS; BIOLOGY; CHYMASE;
D O I
10.3390/ijms24076498
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanisms of ovarian endometrioid cyst formation, or cystic ovarian endometriosis, still remain to be elucidated. To address this issue, we analyzed the involvement of mast cell (MC) tryptase and carboxypeptidase A3 (CPA3) in the development of endometriomas. It was found that the formation of endometrioid cysts was accompanied by an increased MC population in the ovarian medulla, as well as by an MC appearance in the cortical substance. The formation of MC subpopulations was associated with endometrioma wall structures. An active, targeted secretion of tryptase and CPA3 to the epithelium of endometrioid cysts, immunocompetent cells, and the cells of the cytogenic ovarian stroma was detected. The identification of specific proteases in the cell nuclei of the ovarian local tissue microenvironment suggests new mechanisms for the regulatory effects of MCs. The cytoplasmic outgrowths of MCs propagate in the structures of the stroma over a considerable distance; they offer new potentials for MC effects on the structures of the ovarian-specific tissue microenvironment under pathological conditions. Our findings indicate the potential roles of MC tryptase and CPA3 in the development of ovarian endometriomas and infer new perspectives on their uses as pharmacological targets in personalized medicine.
引用
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页数:19
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