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Sci Adv. 2022 May 27;8(21):eabj8892. doi: 10.1126/sciadv.abj8892. Epub 2022 May 25.
2
Hypoxia impacts human MSC response to substrate stiffness during chondrogenic differentiation.缺氧会影响人骨髓间充质干细胞在软骨分化过程中对基质硬度的反应。
Acta Biomater. 2019 Apr 15;89:73-83. doi: 10.1016/j.actbio.2019.03.002. Epub 2019 Mar 4.
3
Engineering hyaline cartilage from mesenchymal stem cells with low hypertrophy potential via modulation of culture conditions and Wnt/β-catenin pathway.通过调控培养条件和 Wnt/β-catenin 通路,利用低肥大潜能的间充质干细胞工程化透明软骨。
Biomaterials. 2019 Feb;192:569-578. doi: 10.1016/j.biomaterials.2018.11.036. Epub 2018 Nov 30.
4
A MMP7-sensitive photoclickable biomimetic hydrogel for MSC encapsulation towards engineering human cartilage.一种 MMP7 敏感的光点击仿生水凝胶,用于 MSC 包封以工程化人软骨。
J Biomed Mater Res A. 2018 Aug;106(8):2344-2355. doi: 10.1002/jbm.a.36412. Epub 2018 Apr 30.
5
Deletion of Runx2 in Articular Chondrocytes Decelerates the Progression of DMM-Induced Osteoarthritis in Adult Mice.软骨细胞中 Runx2 的缺失可延缓成年小鼠 DMM 诱导的骨关节炎的进展。
Sci Rep. 2017 May 24;7(1):2371. doi: 10.1038/s41598-017-02490-w.
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Phosphate regulates chondrogenesis in a biphasic and maturation-dependent manner.磷酸盐以双相且依赖成熟的方式调节软骨形成。
Differentiation. 2017 May-Jun;95:54-62. doi: 10.1016/j.diff.2017.04.002. Epub 2017 May 8.
7
Genome Engineering of Stem Cells for Autonomously Regulated, Closed-Loop Delivery of Biologic Drugs.干细胞的基因组工程,用于自主调节、闭环输送生物药物。
Stem Cell Reports. 2017 May 9;8(5):1202-1213. doi: 10.1016/j.stemcr.2017.03.022. Epub 2017 Apr 27.
8
CRISPR/Cas9 Editing of Murine Induced Pluripotent Stem Cells for Engineering Inflammation-Resistant Tissues.CRISPR/Cas9 编辑小鼠诱导多能干细胞用于工程化炎症抗性组织。
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9
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10
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用于在软骨生成过程中自主调节 RUNX2 活性的合成、闭环基因回路。

A synthetic, closed-looped gene circuit for the autonomous regulation of RUNX2 activity during chondrogenesis.

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.

Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

FASEB J. 2024 Feb 29;38(4):e23484. doi: 10.1096/fj.202300348RR.

DOI:10.1096/fj.202300348RR
PMID:38407380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10981937/
Abstract

The transcription factor RUNX2 is a key regulator of chondrocyte phenotype during development, making it an ideal target for prevention of undesirable chondrocyte maturation in cartilage tissue-engineering strategies. Here, we engineered an autoregulatory gene circuit (cisCXp-shRunx2) that negatively controls RUNX2 activity in chondrogenic cells via RNA interference initiated by a tunable synthetic Col10a1-like promoter (cisCXp). The cisCXp-shRunx2 gene circuit is designed based on the observation that induced RUNX2 silencing after early chondrogenesis enhances the accumulation of cartilaginous matrix in ATDC5 cells. We show that the cisCXp-shRunx2 initiates RNAi of RUNX2 in maturing chondrocytes in response to the increasing intracellular RUNX2 activity without interfering with early chondrogenesis. The induced loss of RUNX2 activity in turn negatively regulates the gene circuit itself. Moreover, the efficacy of RUNX2 suppression from cisCXp-shRunx2 can be controlled by modifying the sensitivity of cisCXp promoter. Finally, we show the efficacy of inhibiting RUNX2 in preventing matrix loss in human mesenchymal stem cell-derived (hMSC-derived) cartilage under conditions that induce chondrocyte hypertrophic differentiation, including inflammation. Overall, our results demonstrated that the negative modulation of RUNX2 activity with our autoregulatory gene circuit enhanced matrix synthesis and resisted ECM degradation by reprogrammed MSC-derived chondrocytes in response to the microenvironment of the degenerative joint.

摘要

转录因子 RUNX2 是发育过程中软骨细胞表型的关键调节因子,使其成为软骨组织工程策略中预防软骨细胞成熟不良的理想靶点。在这里,我们构建了一个自调节基因回路(cisCXp-shRunx2),该基因回路通过由可调合成 Col10a1 样启动子(cisCXp)启动的 RNA 干扰来负调控软骨细胞中的 RUNX2 活性。cisCXp-shRunx2 基因回路的设计基于这样的观察结果,即在早期成软骨后诱导 RUNX2 沉默会增强 ATDC5 细胞中软骨基质的积累。我们表明,cisCXp-shRunx2 会在成熟的软骨细胞中响应细胞内 RUNX2 活性的增加而引发 RUNX2 的 RNAi,而不会干扰早期成软骨。RUNX2 活性的诱导丧失反过来又负调节基因回路本身。此外,cisCXp 启动子敏感性的改变可以控制 cisCXp-shRunx2 抑制 RUNX2 的效果。最后,我们表明,在诱导软骨细胞肥大分化的条件下,包括炎症,cisCXp-shRunx2 抑制 RUNX2 的功效可防止人骨髓间充质干细胞来源(hMSC 来源)软骨中的基质丢失。总的来说,我们的结果表明,我们的自调节基因回路对 RUNX2 活性的负调控增强了基质合成,并抵抗了 ECM 的降解,从而响应退行性关节的微环境重新编程 MSC 来源的软骨细胞。