Department of Laboratory Medicine, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230001, China.
Core Unit of National Clinical Research Center for Laboratory Medicine, Hefei 230001, China.
ACS Biomater Sci Eng. 2024 Sep 9;10(9):5784-5795. doi: 10.1021/acsbiomaterials.4c00622. Epub 2024 Aug 20.
Extracellular vesicles derived from mesenchymal stem cells (MSCs-EVs) have great potential for bone remodeling and anti-inflammatory therapy. For the repair and reconstruction of inflammatory jawbone defects caused by periapical periodontitis, bone meal filling after debridement is commonly used in the clinic. However, this treatment has disadvantages such as large individual differences and the need for surgical operation. Therefore, it is of great significance to search for other bioactive substances that can promote jawbone regeneration in periapical periodontitis. Herein, it is found that CT results showed that local injection of human umbilical cord mesenchymal stem cells-derived extracellular vesicles (HUC-MSCs-EVs) and bone meal filling into the alveolar bone defect area could promote bone tissue regeneration using a rat model of a jawbone defect in periapical periodontitis. Histologically, the new periodontal tissue in the bone defect area was thicker, and the number of blood vessels was higher by local injection of HUC-MSCs-EVs, and fewer inflammatory cells and osteoclasts were formed compared to bone meal filling. In vitro, HUC-MSCs-EVs can be internalized by rat bone marrow mesenchymal stem cells (BMSCs), enhancing the ability for proliferation and migration of BMSCs. Additionally, 20 μg/mL HUC-MSCs-EVs can facilitate the expression of osteogenic genes and proteins including runt-related transcription factor 2 (RUNX2), alkaline phosphatase (ALP), and osteopontin (OPN). In summary, in vivo and in vitro experiments showed that HUC-MSCs-EVs can promote bone regeneration in periapical periodontitis, and the effect of tissue regeneration is better than that of traditional bone meal treatment. Therefore, local injection of HUC-MSCs-EVs may be an effective method to promote jawbone regeneration in periapical periodontitis.
间充质干细胞来源的细胞外囊泡(MSCs-EVs)在骨重塑和抗炎治疗方面具有巨大潜力。对于由根尖周炎引起的炎性颌骨缺损的修复和重建,临床上通常采用清创后骨粉填充的方法。然而,这种治疗方法存在个体差异大、需要手术等缺点。因此,寻找其他可促进根尖周炎颌骨再生的生物活性物质具有重要意义。在此,研究人员发现 CT 结果显示,局部注射人脐带间充质干细胞来源的细胞外囊泡(HUC-MSCs-EVs)和骨粉填充到牙槽骨缺损区域,可以促进大鼠模型中根尖周炎颌骨缺损部位的骨组织再生。组织学上,与骨粉填充相比,局部注射 HUC-MSCs-EVs 可使骨缺损区域的牙周新组织更厚,血管数量更高。此外,体外实验结果表明,HUC-MSCs-EVs 可以被大鼠骨髓间充质干细胞(BMSCs)内化,增强 BMSCs 的增殖和迁移能力。此外,20μg/mL 的 HUC-MSCs-EVs 可以促进成骨基因和蛋白的表达,包括 runt 相关转录因子 2(RUNX2)、碱性磷酸酶(ALP)和骨桥蛋白(OPN)。综上所述,体内和体外实验表明,HUC-MSCs-EVs 可以促进根尖周炎中的骨再生,其组织再生效果优于传统的骨粉治疗。因此,局部注射 HUC-MSCs-EVs 可能是促进根尖周炎颌骨再生的一种有效方法。