Enhancement of functional insulin-producing cell differentiation from embryonic stem cells through MST1-silencing.

IF 3.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Hui Song, Jiarui Li, Haohao Yang, Bin Kong, Yu Xu, Xiong Li, Hui Li
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引用次数: 0

Abstract

Background: Islet β-cell transplantation offers a promising treatment for repairing pancreatic damage in diabetes, with the transcription factor pancreatic duodenal homeobox-1 (PDX1) being crucial for β-cell function and insulin secretion. Mammalian threonine protein kinase (MST1) is recognized for its role in regulating PDX1 during cell apoptosis, yet its function in embryonic stem cell (ESC) differentiation into insulin-producing cells (IPCs) remain underexplored. This study investigated the effect of MST1-silencing on the differentiation of ESC into IPCs.

Methods: ESCs were transfected utilizing a recombinant MST1-silencing lentiviral vector (shMST1). qRT-PCR, immunofluorescence, flow cytometry, western blot and ELISA assays were performed to examine function of IPCs in vitro. Furthermore, these IPCs were transplanted into type 1 diabetic mellitus (T1DM) rats. Measuring the changes in blood glucose concentration of animals before and after IPCs transplantation. Intraperitoneal glucose tolerance test (IPGT) was used to determine the regulatory effect of IPCs transplantation on blood glucose stimulation and immunohistochemistry was used to detect the expression of pancreatic Insulin protein in T1DM rats.

Results: It was observed that IPCs from the shMST1 group exhibited notably improvement in insulin secretion and glucose responsiveness, suggesting MST1 suppression may enhance IPC maturity. The rats demonstrated significant normalization of blood sugar levels and increased insulin levels, akin to non-diabetic controls. This implies that MST1-silencing not only augments IPC function in vitro but also their therapeutic efficacy in vivo.

Conclusions: The findings indicate that targeting MST1 offers a novel approach for deriving functionally mature IPCs from ESCs, potentially advancing cell replacement therapies for diabetes. This research underscores the importance of developing IPCs with competent insulin secretion for diabetes treatment in vitro.

通过mst1沉默增强胚胎干细胞的功能性胰岛素生成细胞分化。
胰岛β细胞移植是一种很有前景的治疗糖尿病胰腺损伤的方法,转录因子胰十二指肠同源盒-1 (PDX1)对β细胞功能和胰岛素分泌至关重要。哺乳动物苏氨酸蛋白激酶(MST1)被认为在细胞凋亡过程中调节PDX1的作用,但其在胚胎干细胞(ESC)向胰岛素生成细胞(IPCs)分化中的功能仍未得到充分研究。本研究探讨mst1沉默对ESC向IPCs分化的影响。方法:利用重组mst1沉默慢病毒载体(shMST1)转染ESCs。采用qRT-PCR、免疫荧光、流式细胞术、western blot、ELISA等方法检测IPCs的体外功能。此外,将这些IPCs移植到1型糖尿病(T1DM)大鼠体内。测定造血干细胞移植前后动物血糖浓度的变化。采用腹腔糖耐量试验(IPGT)检测IPCs移植对T1DM大鼠血糖刺激的调节作用,免疫组织化学检测胰腺胰岛素蛋白的表达。结果:我们观察到shMST1组IPCs的胰岛素分泌和葡萄糖反应性明显改善,提示抑制MST1可能会提高IPC成熟度。这些大鼠表现出血糖水平明显正常化,胰岛素水平升高,与非糖尿病对照组相似。这表明mst1沉默不仅可以增强IPC的体外功能,还可以增强其体内的治疗效果。结论:研究结果表明,靶向MST1为从ESCs中获得功能成熟的IPCs提供了一种新的方法,可能会推进糖尿病的细胞替代疗法。这项研究强调了开发具有胰岛素分泌能力的IPCs在体外治疗糖尿病的重要性。
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来源期刊
Diabetology & Metabolic Syndrome
Diabetology & Metabolic Syndrome ENDOCRINOLOGY & METABOLISM-
CiteScore
6.20
自引率
0.00%
发文量
170
审稿时长
7.5 months
期刊介绍: Diabetology & Metabolic Syndrome publishes articles on all aspects of the pathophysiology of diabetes and metabolic syndrome. By publishing original material exploring any area of laboratory, animal or clinical research into diabetes and metabolic syndrome, the journal offers a high-visibility forum for new insights and discussions into the issues of importance to the relevant community.
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