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父源胰岛素样生长因子2(Igf2)在成年期调节干细胞活性。

Paternal Insulin-like Growth Factor 2 (Igf2) Regulates Stem Cell Activity During Adulthood.

作者信息

Barroca Vilma, Lewandowski Daniel, Jaracz-Ros Agnieszka, Hardouin Sylvie-Nathalie

机构信息

INSERM UMR 967, 92265 Fontenay-aux-roses cedex, France; CEA/DSV/iRCM, 92265 Fontenay-aux-roses cedex, France; Université Paris-Diderot, Paris 7, 92265 Fontenay-aux-roses cedex, France; Université Paris-Sud, Paris 11, 92265 Fontenay-aux-roses cedex, France.

INSERM UMR 967, 92265 Fontenay-aux-roses cedex, France; CEA/DSV/iRCM, 92265 Fontenay-aux-roses cedex, France; Université Paris-Diderot, Paris 7, 92265 Fontenay-aux-roses cedex, France; Université Paris-Sud, Paris 11, 92265 Fontenay-aux-roses cedex, France.

出版信息

EBioMedicine. 2017 Feb;15:150-162. doi: 10.1016/j.ebiom.2016.11.035. Epub 2016 Dec 3.

Abstract

Insulin-like Growth Factor 2 (IGF2) belongs to the IGF/Insulin pathway, a highly conserved evolutionarily network that regulates growth, aging and lifespan. Igf2 is highly expressed in the embryo and in cancer cells. During mouse development, Igf2 is expressed in all sites where hematopoietic stem cells (HSC) successively expand, then its expression drops at weaning and becomes undetectable when adult HSC have reached their niches in bones and start to self-renew. In the present study, we aim to discover the role of IGF2 during adulthood. We show that Igf2 is specifically expressed in adult HSC and we analyze HSC from adult mice deficient in Igf2 transcripts. We demonstrate that Igf2 deficiency avoids the age-related attrition of the HSC pool and that Igf2 is necessary for tissue homeostasis and regeneration. Our study reveals that the expression level of Igf2 is critical to maintain the balance between stem cell self-renewal and differentiation, presumably by regulating the interaction between HSC and their niche. Our data have major clinical interest for transplantation: understanding the changes in adult stem cells and their environments will improve the efficacy of regenerative medicine and impact health- and life-span.

摘要

胰岛素样生长因子2(IGF2)属于IGF/胰岛素信号通路,这是一个在进化上高度保守的网络,可调节生长、衰老和寿命。Igf2在胚胎和癌细胞中高表达。在小鼠发育过程中,Igf2在造血干细胞(HSC)相继扩增的所有部位均有表达,然后其表达在断奶时下降,当成年HSC到达骨髓龛位并开始自我更新时则无法检测到。在本研究中,我们旨在发现IGF2在成年期的作用。我们发现Igf2在成年HSC中特异性表达,并分析了缺乏Igf2转录本的成年小鼠的HSC。我们证明,Igf2缺乏可避免HSC库的年龄相关损耗,并且Igf2对于组织稳态和再生是必需的。我们的研究表明,Igf2的表达水平对于维持干细胞自我更新和分化之间的平衡至关重要,可能是通过调节HSC与其龛位之间的相互作用来实现的。我们的数据对移植具有重要的临床意义:了解成体干细胞及其环境的变化将提高再生医学的疗效,并影响健康和寿命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b15d/5233811/3474dfb820b6/fx1.jpg

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