Lan B Y, Lin X, Chen W J, Xie J, Chen W X
Department of Operative Dentistry and Endodontics, College & Hospital of Stomatology, Guangxi Medical University & Guangxi Health Commission Key Laboratory of Prevention and Treatment for Oral Infectious Diseases & Guangxi Key Laboratory of Oral and Maxillofacial Rehabilitation and Reconstruction, Nanning 530021, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2022 Jan 9;57(1):60-67. doi: 10.3760/cma.j.cn112144-20210911-00408.
To investigate the effect of exosomes from mild-inflammation- stimulated human dental pulp stem cells (hDPSC) combined with stromal cell-derived factor-1 (SDF-1) on dental pulp regeneration in rats. Primary hDPSCs were isolated, cultured and then stimulated by using lipopolysaccharide (LPS). The exosomes from the hDPSCs with (L-EXO) or without (N-EXO) LPS were extracted by overspeed differential centrifugation and were identified by transmission electron microscopy and Western blotting. Forty SD rats, aged 6-8 weeks, were equally divided into S group (SDF-1 alone), L+S group (L-EXO combined with SDF-1), N+S group (N-EXO combined with SDF-1) and blank control group (no substance implanted into the root canal) by random number table method. Bilateral mandibular first molars were used as the experimental teeth to establish pulpless root canal models and different contents were implanted into the root canals according to the groups. All rats were over-anesthetized and sacrificed at the 30th day after content implantation. Bilateral mandibular tissues were taken for histological evaluation by means of HE, Masson and immunohistochemical stainings. The HE staining showed new pulp-like tissue in the root canals of all three experimental groups. The amount of new tissues and the number of cells in the tissues were greatest in L+S group and least in S group. Masson staining showed that the mineralized tissue in L+S group was arranged longitudinally along the root canal wall and the collagen fibers were arranged in an orderly fashion, while those in N+S group showed an irregular and disordered distribution. Quantitative analysis of the area of neovascularization in each group showed that the density of vessels in the L+S group [(2.03±0.65)%] was significantly higher than that in the S group [(0.65±0.05)%] and the N+S group [(1.06±0.38)%] respectively (=5.879, <0.05). Immunohistochemical staining showed that the expression of CXC chemokine receptor 4 (CXCR4) was significantly lower in S and L+S groups than in N+S group, with a statistically significant difference (=8.633, <0.01). Exosomes secreted by hDPSCs combined with SDF-1 might increase the amount of new tissue in the root canal and the density of blood vessels in the tissue. L-EXO showed a stronger effect than N-EXO did. The combination of L-EXO with SDF-1 might result in more regular arrangement of mineralized tissue and collagen fibers in the regenerative tissues.
探讨轻度炎症刺激的人牙髓干细胞(hDPSC)来源的外泌体联合基质细胞衍生因子-1(SDF-1)对大鼠牙髓再生的影响。分离、培养原代hDPSC,然后用脂多糖(LPS)进行刺激。采用超速差速离心法提取经LPS刺激(L-EXO)和未经LPS刺激(N-EXO)的hDPSC来源的外泌体,并通过透射电子显微镜和蛋白质免疫印迹法进行鉴定。将40只6-8周龄的SD大鼠通过随机数字表法分为S组(单纯SDF-1)、L+S组(L-EXO联合SDF-1)、N+S组(N-EXO联合SDF-1)和空白对照组(根管内未植入任何物质)。以双侧下颌第一磨牙作为实验牙,建立牙髓摘除根管模型,并按组将不同内容物植入根管。所有大鼠在植入物植入后第30天过量麻醉并处死。取双侧下颌组织进行苏木精-伊红(HE)、马松(Masson)和免疫组织化学染色以进行组织学评估。HE染色显示,所有三个实验组的根管内均有新的牙髓样组织。L+S组新组织的量和组织中的细胞数量最多,S组最少。Masson染色显示,L+S组矿化组织沿根管壁纵向排列,胶原纤维排列有序,而N+S组则呈不规则和无序分布。对各组新生血管面积的定量分析显示,L+S组血管密度[(2.03±0.65)%]分别显著高于S组[(0.65±0.05)%]和N+S组[(1.06±0.38)%](F=5.879,P<0.05)。免疫组织化学染色显示,S组和L+S组中CXC趋化因子受体4(CXCR4)的表达显著低于N+S组,差异有统计学意义(F=8.633,P<0.01)。hDPSC分泌的外泌体联合SDF-1可能会增加根管内新组织的量和组织内血管的密度。L-EXO的作用强于N-EXO。L-EXO与SDF-1联合可能会使再生组织中的矿化组织和胶原纤维排列更规则。