Ma Cheng, Tao Chao, Zhang Zhen, Zhou Huiqun, Fan Changjiang, Wang Dong-An
Department of Biomedical Engineering, College of Engineering, City University of Hong Kong, Hong Kong.
Karolinska Institutet Ming Wai Lau Centre for Reparative Medicine, HKSTP, Sha Tin, Hong Kong.
Mater Today Bio. 2023 Dec 3;23:100893. doi: 10.1016/j.mtbio.2023.100893. eCollection 2023 Dec.
Endochondral ossification (ECO) is a form of bone formation whereby the newly deposited bone replaces the cartilage template. A decellularized artificial cartilage graft (dLhCG), which is composed of hyaline cartilage matrixes, has been developed in our previous study. Herein, the osteogenesis of bone marrow-derived MSCs in the dLhCG through chondrogenic differentiation, chondrocyte hypertrophy, and subsequent transdifferentiation induction has been investigated by simulating the physiological processes of ECO for repairing critical-sized bone defects. The MSCs were recellularized into dLhCGs and subsequently allowed to undergo a 14-day proliferation period (mrLhCG). Following this, the mrLhCG constructs were subjected to two distinct differentiation induction protocols to achieve osteogenic differentiation: chondrogenic medium followed by chondrocytes culture medium with a high concentration of fetal bovine serum (CGCC group) and canonical osteogenesis inducing medium (OI group). The formation of a newly developed artificial bone graft, ossified dLhCG (OsLhCG), as well as its capability of aiding bone defect reconstruction were characterized by and trials, such as mRNA sequencing, quantitative real-time PCR (qPCR), immunohistochemistry, the greater omentum implantation in nude mice, and repair for the critical-sized femoral defects in rats. The results reveal that the differentiation induction of MSCs in the CGCC group can realize ECO through chondrogenic differentiation, hypertrophy, and transdifferentiation, while the MSCs in the OI group, as expected, realize ossification through direct osteogenic differentiation. The angiogenesis and osteogenesis of OsLhCG were proved by being implanted into the greater omentum of nude mice. Besides, the OsLhCG exhibits the capability to achieve the repair of critical-size femoral defects.
软骨内成骨(ECO)是一种骨形成形式,新沉积的骨替代软骨模板。在我们之前的研究中,已经开发出一种由透明软骨基质组成的脱细胞人工软骨移植物(dLhCG)。在此,通过模拟ECO的生理过程以修复临界尺寸骨缺损,研究了骨髓间充质干细胞(MSCs)在dLhCG中通过软骨形成分化、软骨细胞肥大及随后的转分化诱导的成骨过程。将MSCs重新接种到dLhCG中,随后使其经历14天的增殖期(mrLhCG)。在此之后,对mrLhCG构建体进行两种不同的分化诱导方案以实现成骨分化:软骨形成培养基随后是含有高浓度胎牛血清的软骨细胞培养基(CGCC组)和经典成骨诱导培养基(OI组)。通过mRNA测序、定量实时PCR(qPCR)免疫组织化学、裸鼠大网膜植入以及大鼠临界尺寸股骨缺损修复等试验,对新开发的人工骨移植物——骨化dLhCG(OsLhCG)的形成及其辅助骨缺损重建的能力进行了表征。结果表明,CGCC组中MSCs 的分化诱导可通过软骨形成分化、肥大和转分化实现ECO,而OI组中的MSCs如预期那样通过直接成骨分化实现骨化。将OsLhCG植入裸鼠大网膜证明了其血管生成和成骨能力。此外,OsLhCG表现出实现临界尺寸股骨缺损修复的能力。