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锌指蛋白2(Zhx2)通过转录调控配对盒基因6(Pax6)来维持胰岛β细胞数量和功能。

Zhx2 maintains islet β-cell mass and function by transcriptionally regulating Pax6.

作者信息

Ding Lu, Zhang Yankun, Wang Yingchun, Wang Yuzhen, Tong Zheng, Li Pengfei, Chen Chaojia, Wang Bo, Yue Xuetian, Li Chunyang, Wu Zhuanchang, Liang Xiaohong, Ma Chunhong, Gao Lifen

机构信息

Key Laboratory for Experimental Teratology of Ministry of Education, Shandong Key Laboratory of Infection and Immunity, and Department of Immunology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, P. R. China.

Department of Endocrinology, Yucheng People's Hospital, Dezhou, Shandong 251200, P. R. China.

出版信息

iScience. 2023 May 13;26(6):106871. doi: 10.1016/j.isci.2023.106871. eCollection 2023 Jun 16.

Abstract

Emerging evidence shows that pancreatic β-cell function and quality are key determinants in the progression of type 2 diabetes (T2D). The transcription factor zinc finger homeobox 2 (Zhx2) is involved in proliferation and development of multiple cells. However, the exact role of Zhx2 in β-cells and T2D remains completely unknown. Here, we report that Zhx2 orchestrates β-cell mass and function by regulating paired box protein pax-6 (Pax6). We found that β-cell-specific knockout Zhx2 (Zhx2BKO) mice showed a decrease in β-cell proliferation and glucose homeostasis. Under prediabetic and diabetic conditions, we discovered glucose intolerance in both Zhx2BKO-HFD mice and Zhx2BKO-db/db mice, with reduced β-cell mass and insulin secretion. Mechanistically, we demonstrated that Zhx2 targeted the Pax6 promoter region (-1740∼-1563; -862∼-559; -251∼+75), enhanced promoter activity. Overall, Zhx2 maintains β-cell function by transcriptionally regulating Pax6, which provides a therapeutic target for diabetes intervention.

摘要

新出现的证据表明,胰腺β细胞功能和质量是2型糖尿病(T2D)进展的关键决定因素。转录因子锌指同源框2(Zhx2)参与多种细胞的增殖和发育。然而,Zhx2在β细胞和T2D中的确切作用仍完全未知。在此,我们报告Zhx2通过调节配对盒蛋白Pax-6(Pax6)来协调β细胞质量和功能。我们发现β细胞特异性敲除Zhx2(Zhx2BKO)小鼠的β细胞增殖和葡萄糖稳态降低。在糖尿病前期和糖尿病条件下,我们在Zhx2BKO-HFD小鼠和Zhx2BKO-db/db小鼠中均发现葡萄糖不耐受,β细胞质量和胰岛素分泌减少。从机制上讲,我们证明Zhx2靶向Pax6启动子区域(-1740∼-1563;-862∼-559;-251∼+75),增强启动子活性。总体而言,Zhx2通过转录调控Pax6维持β细胞功能,这为糖尿病干预提供了一个治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c32/10232729/80c7e59aeccb/fx1.jpg

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