Thamm Janis R, Jounaidi Youssef, Mueller Max-Laurin, Rosen Vicki, Troulis Maria J, Guastaldi Fernando Pozzi Semeghini
Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital, Harvard School of Dental Medicine, Boston, MA USA.
Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
J Maxillofac Oral Surg. 2023 Sep;22(3):559-570. doi: 10.1007/s12663-022-01721-6. Epub 2022 May 9.
A specific type of mesenchymal stem/progenitor cells (MSPCs), CD105 is reported to aid in cartilage regeneration through TGF-β/Smad2-signalling. The purpose of this study was to identify and characterize CD105 MSPCs in temporomandibular joint (TMJ) cartilage.
MSPCs were isolated from mouse TMJ condyle explants and evaluated for their clonogenicity and pluripotential abilities. MSPC were examined for CD105 antigen using immunohistochemistry and flow cytometry.
Immunohistochemistry revealed presence of CD105 MSPCs in the proliferative zone of condyle's cartilage. Only 0.2% of isolated MSPCs exhibited CD105, along with the stem cell surface markers CD44 and Sca-1. In CD105 MSPCs, intracellular immunostaining revealed significantly higher ( < 0.05) protein levels of collagen type 1, 2, proteoglycan 4. Ability for chondrogenic differentiation was found to be significantly higher ( < 0.05) after 4 weeks compared to CD105 cells, using alcian blue staining. CD105 cells were found to resemble an early MSPC subgroup with significantly higher gene expression of biglycan, proteoglycan 4, collagen type 2, Gli2, Sox5 ( < 0.001) and Sox9 ( < 0.05). In contrast, significantly lower levels of Runx2 ( < 0.05), Osterix, Trps1, Col10a1 ( < 0.01), Ihh ( < 0.001) related to chondrocyte senescence and commitment to osteogenic lineage, were observed compared to CD105 cells.
The study showed the existence of a CD105 MSPC subgroup within TMJ fibrocartilage that may be activated to aid in fibrocartilage repair.
据报道,一种特定类型的间充质干/祖细胞(MSPCs),即CD105,可通过TGF-β/Smad2信号通路促进软骨再生。本研究的目的是鉴定和表征颞下颌关节(TMJ)软骨中的CD105 MSPCs。
从小鼠TMJ髁突外植体中分离出MSPCs,并评估其克隆形成能力和多能性。使用免疫组织化学和流式细胞术检测MSPCs中的CD105抗原。
免疫组织化学显示髁突软骨增殖区存在CD105 MSPCs。分离出的MSPCs中只有0.2%表现出CD105,同时还伴有干细胞表面标志物CD44和Sca-1。在CD105 MSPCs中,细胞内免疫染色显示I型、II型胶原蛋白、蛋白聚糖4的蛋白水平显著更高(<0.05)。与CD105细胞相比,使用阿尔辛蓝染色法发现,4周后CD105 MSPCs的软骨形成分化能力显著更高(<0.05)。发现CD105细胞类似于早期MSPC亚组,其双糖链蛋白聚糖、蛋白聚糖4、II型胶原蛋白、Gli2、Sox5(<0.001)和Sox9(<0.05)的基因表达显著更高。相比之下,与软骨细胞衰老和成骨谱系定向相关的Runx2(<0.05)、osterix、Trps1、Col10a1(<0.01)、Ihh(<0.001)水平与CD105细胞相比显著更低。
该研究表明TMJ纤维软骨中存在CD105 MSPC亚组,其可能被激活以促进纤维软骨修复。