miR-199b-5p enhances the proliferation of medullary thymic epithelial cells via regulating Wnt signaling by targeting Fzd6

被引:8
|
作者
Wang, Xintong [1 ]
Li, Ying [1 ]
Gong, Bishuang [1 ]
Zhang, Kaizhao [1 ]
Ma, Yongjiang [1 ]
Li, Yugu [1 ]
机构
[1] South China Agr Univ, Coll Vet Med, Guangzhou 510642, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-199b-5p; thymic epithelial cell; cell proliferation; Fzd6; Wnt signaling; AGE-RELATED-CHANGES; EXPRESSION; INVOLUTION; FOXN1; MICRORNA-199B-5P; PROGENITORS; PREVENTS; PATHWAY;
D O I
10.1093/abbs/gmaa145
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
Thymic epithelial cells (TECs) are essential regulators of T-cell development and selection. miRNAs play critical roles in regulating TEC proliferation during the process of thymic aging. Our previous studies revealed that miR-199b-5p was upregulated in TECs from 1- to 3-month-old mice. But its function and potential mechanism are not clear. We hypothesized that miR-199b-5p may play an important role in age-related thymus involution via targeting some genes. To confirm it, the murine thymic epithelial cell line 1 (MTEC1) cells were used. Our results showed that overexpression of miR-199b-5p can enhance MTEC1 cell proliferation. On the contrary, repression of miR-199b-5p can inhibit MTEC1 cell proliferation. Meanwhile, it was confirmed that frizzled receptor 6 (Fzd6) is the direct target gene of miR-199b-5p. Furthermore, overexpression of miR-199b-5p can upregulate the expressions of beta-catenin, Tcf7, Wnt4, and C-myc to activate Wnt signaling and cell cycle signaling. Silence of Fzd6 and co-transfection with siFzd6 and miR-199b-5p mimic/inhibitor confirmed that the biological function of miR-199b-5p is indeed by targeting Fzd6 in medullary TECs. Overall, miR-199b-5p is an important regulator in medullary TEC proliferation through targeting Fzd6 to activate Wnt signaling and cell cycle signaling. Our data indicate that miR-199b-5p may block the process of thymic aging and be a potential therapeutic target for thymus involution.
引用
收藏
页码:36 / 45
页数:10
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