Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan, USA.
FASEB J. 2024 Feb 29;38(4):e23484. doi: 10.1096/fj.202300348RR.
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.
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。