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首页> 外文期刊>Science Advances >Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
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Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458

机译:通过通过LNCRNA LINC00458调节SMAD2 / 3,对基质刚度的控制促进内胚层谱图规范

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摘要

During endoderm formation, cell identity and tissue morphogenesis are tightly controlled by cell-intrinsic and cell-extrinsic factors such as biochemical and physical inputs. While the effects of biochemical factors are well studied, the physical cues that regulate cell division and differentiation are poorly understood. RNA sequencing analysis demonstrated increases of endoderm-specific gene expression in hPSCs cultured on soft substrate (Young’s modulus, 3 ± 0.45 kPa) in comparison with hard substrate (Young’s modulus, 165 ± 6.39 kPa). Further analyses revealed that multiple long noncoding RNAs (lncRNAs) were up-regulated on soft substrate; among them, LINC00458 was identified as a stiffness-dependent lncRNA specifically required for hPSC differentiation toward an early endodermal lineage. Gain- and loss-of-function experiments confirmed that LINC00458 is functionally required for hPSC endodermal lineage specification induced by soft substrates. Our study provides evidence that mechanical cues regulate the expression of LINC00458 and induce differentiation of hPSC into hepatic lineage progenitors.
机译:在内胚层形成期间,细胞同一性和组织形态发生通过细胞内在和细胞外部因子(例如生物化学和物理输入)紧密控制。虽然生物化学因素的影响很好地研究,但调节细胞分裂和分化的物理提示很难理解。 RNA测序分析与硬质基质(杨氏模量,165±6.39kPa)相比,RNA测序分析表明,在软基质(杨氏模量,3±0.45kPa)上培养的HPSC中的细胞特异性基因表达增加。进一步分析显示,在软基材上上调多个长的非分量RNA(LNCRNA);其中,LINC00458被鉴定为HPSC分化朝向早期内胚层谱系的刚度依赖性LNCRNA。函数和丧失损失实验证实,LINC00458在功能上需要由软基板引起的HPSC内胚层谱系规范。我们的研究提供了证据,即机械提示调节LINC00458的表达,并诱导HPSC进入肝脏谱系祖细胞的分化。

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