Karl Chiari Lab for Orthopaedic Biology, Department of Orthopedics and Trauma Surgery, Medical University of Vienna, Vienna, Austria.
Orthopaedic Hospital Speising, Vienna, Austria.
Cartilage. 2021 Dec;13(2_suppl):336S-345S. doi: 10.1177/1947603519865320. Epub 2019 Aug 2.
Functional cartilage repair requires the new formation of organized hyaline cartilaginous matrix to avoid the generation of fibrous repair tissue. The potential of mesenchymal progenitors was used to assemble a 3-dimensional structure in vitro, reflecting the zonation of collagen matrix in hyaline articular cartilage.
The 3-dimensional architecture of collagen alignment in pellet cultures of chondroprogenitors (CPs) was assessed with Picrosirius red staining analyzed under polarized light. In parallel assays, the trilineage capability was confirmed by calcium deposition during osteogenesis by alizarin S staining and alkaline phosphatase staining. Using reverse transcription-quantitative polymerase chain reaction (RT-qPCR), mRNA levels of ALP, RUNX2, and BGLAP were assessed after 21 days of osteoinduction. Lipid droplets were stained with oil red O and adipogenic differentiation was confirmed by RT-qPCR analysis of PPARG and LPL gene expression.
Under conditions promoting the chondrogenic signature in self-assembling constructs, CPs formed an aligned extracellular matrix, positive for glycosaminoglycans and collagen type II, showing developing zonation of birefringent collagen fibers along the cross section of pellets, which reflect the distribution of collagen fibers in hyaline cartilage. Induced osteogenic and adipogenic differentiation confirmed the trilineage potential of CPs.
This model promotes the differentiation and self-organization of postnatal chondroprogenitors, resulting in the formation of zonally organized engineered hyaline cartilage comparable to the 3 zones of native cartilage.
功能性软骨修复需要新形成有组织的透明软骨基质,以避免产生纤维性修复组织。间充质祖细胞的潜力被用于在体外组装三维结构,反映透明关节软骨中胶原基质的分区。
通过偏光下的苦味酸天狼星红染色分析评估软骨祖细胞(CPs)微球培养物中胶原排列的三维结构。在平行实验中,通过茜素红 S 染色和碱性磷酸酶染色在成骨过程中钙沉积来确认三系能力。使用逆转录定量聚合酶链反应(RT-qPCR),在成骨诱导 21 天后评估碱性磷酸酶、RUNX2 和 BGLAP 的 mRNA 水平。用油红 O 染色脂滴,并通过 PPARG 和 LPL 基因表达的 RT-qPCR 分析确认脂肪分化。
在促进自组装构建体中软骨形成特征的条件下,CPs 形成了排列整齐的细胞外基质,对糖胺聚糖和 II 型胶原呈阳性,显示出沿着微球横截面排列的双折射胶原纤维的分区发育,这反映了透明软骨中胶原纤维的分布。诱导的成骨和成脂分化证实了 CPs 的三系潜能。
该模型促进了产后软骨祖细胞的分化和自我组织,形成了有分区组织的工程化透明软骨,类似于天然软骨的 3 个区。