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与糖尿病相关的转录因子PAX4:从基因到功能后果

The Diabetes-Linked Transcription Factor PAX4: From Gene to Functional Consequences.

作者信息

Lorenzo Petra I, Juárez-Vicente Francisco, Cobo-Vuilleumier Nadia, García-Domínguez Mario, Gauthier Benoit R

机构信息

Pancreatic Islet Development and Regeneration Unit, Department of Cell Regeneration and Advanced Therapies, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.

Cell differentiation Lab, Department of Cell Signaling and Dynamics, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.

出版信息

Genes (Basel). 2017 Mar 9;8(3):101. doi: 10.3390/genes8030101.

Abstract

Paired box 4 (PAX4) is a key factor in the generation of insulin producing β-cells during embryonic development. In adult islets, PAX4 expression is sequestered to a subset of β-cells that are prone to proliferation and more resistant to stress-induced apoptosis. The importance of this transcription factor for adequate pancreatic islets functionality has been manifested by the association of mutations in with the development of diabetes, independently of its etiology. Overexpression of this factor in adult islets stimulates β-cell proliferation and increases their resistance to apoptosis. Additionally, in an experimental model of autoimmune diabetes, a novel immunomodulatory function for this factor has been suggested. Altogether these data pinpoint at PAX4 as an important target for novel regenerative therapies for diabetes treatment, aiming at the preservation of the remaining β-cells in parallel to the stimulation of their proliferation to replenish the β-cell mass lost during the progression of the disease. However, the adequate development of such therapies requires the knowledge of the molecular mechanisms controlling the expression of PAX4 as well as the downstream effectors that could account for PAX4 action.

摘要

配对盒4(PAX4)是胚胎发育过程中产生胰岛素的β细胞生成的关键因素。在成年胰岛中,PAX4的表达局限于一部分易于增殖且对应激诱导的凋亡更具抗性的β细胞。该转录因子对胰腺胰岛正常功能的重要性已通过其突变与糖尿病发生的关联得以体现,而与糖尿病的病因无关。在成年胰岛中过表达该因子可刺激β细胞增殖并增强其对凋亡的抗性。此外,在自身免疫性糖尿病的实验模型中,已表明该因子具有一种新的免疫调节功能。总之,这些数据表明PAX4是糖尿病治疗新型再生疗法的重要靶点,旨在在刺激剩余β细胞增殖以补充疾病进展过程中丢失的β细胞量的同时,保护这些细胞。然而,此类疗法的充分发展需要了解控制PAX4表达的分子机制以及可能解释PAX4作用的下游效应器。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1e9/5368705/b392e604bb15/genes-08-00101-g001.jpg

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