Department of Periodontal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3, Kasumi, Minami-Ku, Hiroshima, 734-8553, Japan.
Department of Innovation and Precision Dentistry, Hiroshima University Hospital, 1-2-3, Kasumi, Minami-Ku, Hiroshima, 734-8553, Japan.
Stem Cell Rev Rep. 2023 Aug;19(6):1812-1827. doi: 10.1007/s12015-023-10554-w. Epub 2023 May 11.
Three-dimensional clumps of mesenchymal stem cells (MSCs)/extracellular matrix (ECM) complexes (C-MSCs) can be implanted into tissue defects with no artificial scaffolds. In addition, the cellular properties and characteristics of the ECM in C-MSCs can be regulated in vitro. Most bone formation in the developmental and healing process is due to endochondral ossification, which occurs after bone collar formation surrounding cartilage derived from MSCs. Thus, to develop a rapid and reliable bone-regenerative cell therapy, the present study aimed to generate cartilaginous tissue covered with a mineralized bone collar-like structure from human C-MSCs by combining chondrogenic and osteogenic induction. Human bone marrow-derived MSCs were cultured in xeno-free/serum-free (XF) growth medium. Confluent cells that formed cellular sheets were detached from the culture plate using a micropipette tip. The floating cellular sheet contracted to round clumps of cells (C-MSCs). C-MSCs were maintained in XF-chondro-inductive medium (CIM) and XF-osteo-inductive medium (OIM). The biological and bone-regenerative properties of the generated cellular constructs were assessed in vitro and in vivo. C-MSCs cultured in CIM/OIM formed cartilaginous tissue covered with a mineralized matrix layer, whereas CIM treatment alone induced cartilage with no mineralization. Transplantation of the cartilaginous tissue covered with a mineralized matrix induced more rapid bone reconstruction via endochondral ossification in the severe combined immunodeficiency mouse calvarial defect model than that of cartilage generated using only CIM. These results highlight the potential of C-MSC culture in combination with CIM/OIM to generate cartilage covered with a bone collar-like structure, which can be applied for novel bone-regenerative cell therapy.
三维间质干细胞(MSCs)/细胞外基质(ECM)复合物(C-MSCs)团块可以在没有人工支架的情况下植入组织缺损部位。此外,C-MSCs 中的细胞特性和 ECM 特性可以在体外进行调节。在发育和愈合过程中,大多数骨形成是由于软骨内骨化,这发生在围绕源自 MSCs 的软骨形成骨领之后。因此,为了开发快速可靠的骨再生细胞疗法,本研究旨在通过结合软骨生成和成骨诱导,从人 C-MSCs 生成具有矿化骨领样结构覆盖的软骨组织。人骨髓来源的 MSCs 在无动物源/无血清(XF)生长培养基中培养。达到汇合的形成细胞片的细胞使用微吸管尖端从培养板上分离。漂浮的细胞片收缩成圆形细胞团(C-MSCs)。C-MSCs 保持在 XF-软骨诱导培养基(CIM)和 XF-成骨诱导培养基(OIM)中。在体外和体内评估生成的细胞构建体的生物学和骨再生特性。在 CIM/OIM 中培养的 C-MSCs 形成了覆盖矿化基质层的软骨组织,而单独的 CIM 处理仅诱导了无矿化的软骨。与仅使用 CIM 生成的软骨相比,在严重联合免疫缺陷小鼠颅骨缺损模型中,移植覆盖矿化基质的软骨诱导了更快的骨重建,通过软骨内骨化。这些结果突出了 C-MSC 培养与 CIM/OIM 相结合生成具有骨领样结构覆盖的软骨的潜力,可用于新型骨再生细胞疗法。