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构建细胞力学微环境以调控干细胞软骨生成:来自微凝胶模型的见解

Engineering the cellular mechanical microenvironment to regulate stem cell chondrogenesis: Insights from a microgel model.

作者信息

Feng Qi, Gao Huichang, Wen Hongji, Huang Hanhao, Li Qingtao, Liang Minhua, Liu Yang, Dong Hua, Cao Xiaodong

机构信息

Department of Biomedical Engineering, School of Materials Science and Engineering, South China University of Technology, Guangzhou 510006, China; National Engineering Research Center for Tissue Restoration and Reconstruction (NERC-TRR), Guangzhou 510006, China.

National Engineering Research Center for Tissue Restoration and Reconstruction (NERC-TRR), Guangzhou 510006, China; School of Medicine, South China University of Technology, Guangzhou 510006, China.

出版信息

Acta Biomater. 2020 Sep 1;113:393-406. doi: 10.1016/j.actbio.2020.06.046. Epub 2020 Jul 3.

DOI:10.1016/j.actbio.2020.06.046
PMID:32629189
Abstract

Biophysical cues (especially mechanical cues) embedded in cellular microenvironments show a critical impact on stem cell fate. Despite the capability of traditional hydrogels to mimic the feature of extracellular matrix (ECM) and tune their physicochemical properties via diverse approaches, their relatively large size not only induces biased results, but also hinders high-throughput screening and analysis. In this paper, a microgel model is proposed to recapitulate the role of 3D mechanical microenvironment on stem cell behaviors especially chondrogenesis in vitro. The small diameter of microgels brings the high surface area to volume ratio and then the enlarged diffusion area and shortened diffusion distance of soluble molecules, leading to uniform distribution of nutrients and negligible biochemical gradient inside microgels. To construct ECM-like microenvironment with tunable mechanical strength, three gelatin/hyaluronic acid hybrid microgels with low, medium and high crosslinking densities, i.e., Gel-HA(L), Gel-HA(M) and Gel-HA(H), are fabricated in microfluidic devices by Michael addition reaction between thiolated gelatin (Gel-SH) and ethylsulfated hyaluronic acid (HA-VS) with different substitution degrees of vinyl sulfone groups. Our results show that mouse bone marrow mesenchymal stem cell (BMSC) proliferation, distribution and chondrogenesis are all closely dependent on mechanical microenvironments in microgels. Noteworthily, BMSCs show a clear trend of differentiating into hyaline cartilage in Gel-HA(L) and fibrocartilage in Gel-HA(M) and Gel-HA(H). Whole transcriptome RNA sequencing reveals that mechanical microenvironment of microgels affects BMSC differentiation via TGF-β/Smad signaling pathway, Hippo signaling pathway and Integrin/YAP/TAZ signaling pathway. We believe this microgel model provides a new way to further explore the interaction between cells and 3D microenvironment. STATEMENT OF SIGNIFICANCE: In recent years, hydrogels have been frequently used to construct 3D microenvironment for cells. However, their relatively large size not only brings biased experimental results, but also limits high-throughput screening and analysis. Herein we propose a gelatin/hyaluronic acid microgel model to explore the effects of 3D cellular mechanical microenvironment (biophysical cues) on BMSC behaviors especially chondrogenesis, which can minimize the interference of biochemical gradients. Our results reveal that BMSC differentiation into either hyaline cartilage or fibrocartilage can be regulated via tailoring the mechanical properties of microgels. Whole transcriptome RNA sequencing proves that "TGF-β/Smad signaling pathway", "Hippo signaling pathway" and "Integrins/YAP/ TAZ signaling pathway" are activated or inhibited in this process.

摘要

细胞微环境中嵌入的生物物理线索(尤其是机械线索)对干细胞命运具有关键影响。尽管传统水凝胶能够模拟细胞外基质(ECM)的特征并通过多种方法调节其物理化学性质,但其相对较大的尺寸不仅会导致有偏差的结果,还会阻碍高通量筛选和分析。本文提出了一种微凝胶模型,以概括三维机械微环境对干细胞行为的作用,特别是体外软骨形成。微凝胶的小直径带来了高的表面积与体积比,进而扩大了可溶性分子的扩散面积并缩短了扩散距离,导致微凝胶内部营养物质均匀分布且生化梯度可忽略不计。为了构建具有可调机械强度的类ECM微环境,通过硫醇化明胶(Gel-SH)与具有不同乙烯砜基团取代度的硫酸乙酯化透明质酸(HA-VS)之间的迈克尔加成反应,在微流控装置中制备了三种具有低、中、高交联密度的明胶/透明质酸混合微凝胶,即Gel-HA(L)、Gel-HA(M)和Gel-HA(H)。我们的结果表明,小鼠骨髓间充质干细胞(BMSC)的增殖、分布和软骨形成都紧密依赖于微凝胶中的机械微环境。值得注意的是,BMSC在Gel-HA(L)中表现出分化为透明软骨的明显趋势,而在Gel-HA(M)和Gel-HA(H)中则分化为纤维软骨。全转录组RNA测序表明,微凝胶的机械微环境通过TGF-β/Smad信号通路、Hippo信号通路和整合素/YAP/TAZ信号通路影响BMSC的分化。我们相信这种微凝胶模型为进一步探索细胞与三维微环境之间的相互作用提供了一种新方法。重要性声明:近年来,水凝胶经常被用于构建细胞的三维微环境。然而,它们相对较大的尺寸不仅会带来有偏差的实验结果,还会限制高通量筛选和分析。在此,我们提出一种明胶/透明质酸微凝胶模型,以探索三维细胞机械微环境(生物物理线索)对BMSC行为尤其是软骨形成的影响,这可以最大限度地减少生化梯度的干扰。我们的结果表明,通过调整微凝胶的机械性能,可以调节BMSC向透明软骨或纤维软骨的分化。全转录组RNA测序证明,在此过程中“TGF-β/Smad信号通路”、“Hippo信号通路”和“整合素/YAP/TAZ信号通路”被激活或抑制。

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