Department of Oral and Maxillofacial Surgery, University Medical Center Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Department of Anatomy, Kiel University, Kiel, Germany.
Cartilage. 2023 Jun;14(2):220-234. doi: 10.1177/19476035231154507. Epub 2023 Mar 1.
In autologous chondrocyte implantation (ACI), there is no consensus about used bioscaffolds. The aim of this study was to perform an comparative analysis of 2 clinically applied biomaterials for cartilage lesion treatment.
Monolayer expanded human chondrocytes ( = 6) were embedded in a collagen scaffold (CS) and a hyaluronic acid-based hydrogel (HA). Cells were cultured in chondropermissive medium supplemented with and without interleukin-10 (IL-10) and bone morphogenetic protein-2 (BMP-2). Gene expression of chondrogenic markers (COL1A1, COL2A1, COL10A1, ACAN, SOX9) was detected quantitative real-time-polymerase chain reaction (RT-qPCR). Biosynthesis of matrix compounds, cell viability, morphology as well as migration from surrounding native bovine cartilage into cell-free scaffolds were analyzed histologically. Adhesion of the material to adjacent cartilage was investigated by a custom-made push-out test.
The shift of COL1/2 ratio toward COL2A1 was more pronounced in HA, and cells displayed a more spherical morphology compared with CS. BMP-2 and IL-10 significantly increased COL2A1, SOX9, and ACAN expression, which was paralleled by enhanced staining of glycosaminoglycans (GAGs) and type 2 collagen in histological sections of CS and HA. COL10A1 was not significantly expressed in HA and CS. Better interfacial integration and enhanced cell invasion was observed in CS. Push-out tests using CS showed higher bonding strength to native cartilage.
HA-based hydrogel revealed a more chondrocyte-like phenotype but only allowed limited cell invasion, whereas CS were advantageous in terms of cellular invasion and interfacial adhesion. These differences may be clinically relevant when treating cartilaginous or osteochondral defects.
在自体软骨细胞移植(ACI)中,对于使用的生物支架尚未达成共识。本研究旨在对两种临床应用的软骨病变治疗生物材料进行比较分析。
单层扩增的人软骨细胞(n=6)被嵌入胶原支架(CS)和透明质酸基水凝胶(HA)中。细胞在软骨形成培养基中培养,培养基中添加或不添加白细胞介素-10(IL-10)和骨形态发生蛋白-2(BMP-2)。采用实时定量聚合酶链反应(RT-qPCR)检测软骨形成标志物(COL1A1、COL2A1、COL10A1、ACAN、SOX9)的基因表达。分析基质化合物的生物合成、细胞活力、形态以及从周围天然牛软骨向无细胞支架的迁移情况。通过定制的推出试验分析材料与相邻软骨的粘附情况。
与 CS 相比,HA 中 COL1/2 比值向 COL2A1 的转移更为明显,细胞形态呈更球形。BMP-2 和 IL-10 显著增加了 COL2A1、SOX9 和 ACAN 的表达,CS 和 HA 的组织学切片中糖胺聚糖(GAGs)和 II 型胶原的染色也增强。HA 和 CS 中 COL10A1 表达不显著。CS 中观察到更好的界面整合和增强的细胞入侵。CS 进行的推出试验显示与天然软骨具有更高的结合强度。
基于 HA 的水凝胶显示出更类似软骨细胞的表型,但仅允许有限的细胞入侵,而 CS 在细胞入侵和界面粘附方面具有优势。在治疗软骨或骨软骨缺损时,这些差异可能具有临床意义。