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力与肌腱蛋白聚糖协同促进人胚胎干细胞来源的间充质干细胞向肌腱细胞的定向分化。

Force and scleraxis synergistically promote the commitment of human ES cells derived MSCs to tenocytes.

机构信息

Center for Stem Cell and Tissue Engineering, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Sci Rep. 2012;2:977. doi: 10.1038/srep00977. Epub 2012 Dec 14.

Abstract

As tendon stem/progenitor cells were reported to be rare in tendon tissues, tendons as vulnerable targets of sports injury possess poor self-repair capability. Human ESCs (hESCs) represent a promising approach to tendon regeneration. But their teno-lineage differentiation strategy has yet to be defined. Here, we report that force combined with the tendon-specific transcription factor scleraxis synergistically promoted commitment of hESCs to tenocyte for functional tissue regeneration. Force and scleraxis can independently induce tendon differentiation. However, force alone concomitantly activated osteogenesis, while scleraxis alone was not sufficient to commit, but augment tendon differentiation. Scleraxis synergistically augmented the efficacy of force on teno-lineage differentiation and inhibited the osteo-lineage differentiation by antagonized BMP signaling cascade. The findings not only demonstrated a novel strategy of directing hESC differentiation to tenocyte for functional tendon regeneration, but also offered insights into understanding the network of force, scleraxis and bmp2 controlling tendon-lineage differentiation.

摘要

由于肌腱干细胞/祖细胞在肌腱组织中较为罕见,因此肌腱作为运动损伤的脆弱靶点,自我修复能力较差。人胚胎干细胞(hESCs)是肌腱再生的一种很有前途的方法。但它们的肌腱谱系分化策略尚未确定。在这里,我们报告说,力与肌腱特异性转录因子 Scleraxis 协同作用,促进 hESC 向肌腱细胞分化,以实现功能性组织再生。力和 Scleraxis 可以独立诱导肌腱分化。然而,力单独作用会同时激活成骨作用,而 Scleraxis 单独作用不足以诱导分化,但可以增强肌腱分化。Scleraxis 通过拮抗 BMP 信号级联反应,协同增强力对肌腱谱系分化的作用,并抑制成骨谱系分化。这些发现不仅为指导 hESC 向肌腱细胞分化以实现功能性肌腱再生提供了一种新策略,也为理解力、Scleraxis 和 BMP2 控制肌腱谱系分化的网络提供了深入了解。

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