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有丝分裂原协同作用:促进人类β细胞增殖的新途径。

Mitogen Synergy: An Emerging Route to Boosting Human Beta Cell Proliferation.

作者信息

Shcheglova Ekaterina, Blaszczyk Katarzyna, Borowiak Malgorzata

机构信息

Institute of Molecular Biology and Biotechnology, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States.

出版信息

Front Cell Dev Biol. 2022 Jan 27;9:734597. doi: 10.3389/fcell.2021.734597. eCollection 2021.

DOI:10.3389/fcell.2021.734597
PMID:35155441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8829426/
Abstract

Decreased number and function of beta cells are a key aspect of diabetes mellitus (diabetes), a disease that remains an onerous global health problem. Means of restoring beta cell mass are urgently being sought as a potential cure for diabetes. Several strategies, such as beta cell derivation via pluripotent stem cell differentiation or mature somatic cell transdifferentiation, have yielded promising results. Beta cell expansion is another promising strategy, rendered challenging by the very low proliferative capacity of beta cells. Many effective mitogens have been identified in rodents, but the vast majority do not have similar mitogenic effects in human beta cells. Extensive research has led to the identification of several human beta cell mitogens, but their efficacy and specificity remain insufficient. An approach based on the simultaneous application of several mitogens has recently emerged and can yield human beta cell proliferation rates of up to 8%. Here, we discuss recent advances in restoration of the beta cell population, focusing on mitogen synergy, and the contribution of RNA-sequencing (RNA-seq) to accelerating the elucidation of signaling pathways in proliferating beta cells and the discovery of novel mitogens. Together, these approaches have taken beta cell research up a level, bringing us closer to a cure for diabetes.

摘要

β细胞数量减少和功能异常是糖尿病的一个关键特征,糖尿病仍是一个严峻的全球性健康问题。人们迫切寻求恢复β细胞数量的方法,将其作为治疗糖尿病的潜在手段。多种策略,如通过多能干细胞分化或成熟体细胞转分化来获得β细胞,已取得了令人鼓舞的成果。β细胞扩增是另一种有前景的策略,但β细胞极低的增殖能力使其颇具挑战。在啮齿动物中已鉴定出许多有效的促有丝分裂原,但绝大多数在人类β细胞中没有类似的促有丝分裂作用。广泛的研究已鉴定出几种人类β细胞促有丝分裂原,但其有效性和特异性仍不足。一种基于同时应用多种促有丝分裂原的方法最近出现了,可使人类β细胞增殖率高达8%。在此,我们讨论β细胞群体恢复方面的最新进展,重点关注促有丝分裂原协同作用,以及RNA测序(RNA-seq)在加速阐明增殖β细胞信号通路和发现新型促有丝分裂原方面的贡献。总之,这些方法将β细胞研究提升到了一个新水平,使我们离治愈糖尿病更近一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3d/8829426/9ce9ef1e32fe/fcell-09-734597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3d/8829426/dc8c49b9b64a/fcell-09-734597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3d/8829426/9ce9ef1e32fe/fcell-09-734597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3d/8829426/dc8c49b9b64a/fcell-09-734597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3d/8829426/9ce9ef1e32fe/fcell-09-734597-g002.jpg

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Scrt1, a transcriptional regulator of β-cell proliferation identified by differential chromatin accessibility during islet maturation.Scrt1,一种在胰岛成熟过程中通过差异染色质可及性鉴定的β细胞增殖的转录调节剂。
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GLP-1 peptide analogs for targeting pancreatic beta cells.
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Metabolic control of adaptive β-cell proliferation by the protein deacetylase SIRT2.蛋白质脱乙酰酶SIRT2对适应性β细胞增殖的代谢控制
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