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Potential immunomodulatory effects of stem cells from the?apical papilla on Treg conversion in tissue regeneration for regenerative endodontic treatment

机译:干细胞从α底巴乳乳乳细胞的潜在免疫调节作用对再生胸腺治疗组织再生的Treg转化

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Abstract Aim To evaluate the expression of Foxp3‐positive lymphocytes around newly formed tissue after regenerative endodontic treatment ( RET ) in vivo and investigate the effects of stem cells from the?apical papilla ( SCAP ) on the conversion of CD 4 + CD 25 ? T cells to CD 4 + CD 25 + Foxp3 + regulatory T cells (Tregs) in vitro . Methodology Three 6‐month‐old beagles with nine doubled‐rooted premolars in each dog were randomly assigned to the RET group and the control group. RET was performed after apical periodontitis had been induced in the experimental immature teeth. Three months later, the expression of Foxp3 was detected in the histological sections by immunofluorescent staining. Human SCAP and CD 4 + CD 25 ? T cells from mice spleens (1?:?1 and 1?:?5) were co‐cultured in cell–cell contact or in Transwells, respectively, for 24 and 72?h in vitro . The percentage of Tregs was evaluated by flow cytometry. The results were analysed using the?Fisher's exact test and analysis of variance. P? ? 0.05 was regarded as statistically significant. Results Inflammatory cells were present with tissue regeneration in the RET group, and Foxp3‐positive T cells were enriched around the newly formed tissues. SCAP promoted Treg conversion after 72?h in vitro . Cell–cell contact played an important role after the 24 h co‐culture, whilst soluble factors were also involved after 72?h ( P? ? 0.05). Conclusions SCAP promoted the conversion of pro‐inflammatory T cells to Tregs in vitro . Tregs were enriched around the regenerating tissues in the root canals after RET , which may create a suitable immune microenvironment for the differentiation of SCAP . This study provides an underlying mechanism for tissue regeneration during RET .
机译:摘要旨在评估再生牙髓治疗(RET)在体内再生后组织周围的Foxp3阳性淋巴细胞的表达,并研究干细胞从β-顶端乳头(SCAP)对CD 4 + CD 25转化的影响? T细胞到CD 4 + CD 25 + Foxp3 +调节T细胞(Tregs)体外。方法论三个6个月大的猎犬每只狗的一倍加入一倍繁殖的前珠,被随机分配给RET组和对照组。在实验性未成熟牙齿中诱导顶端牙周炎后进行RET。三个月后,通过免疫荧光染色在组织学区中检测到Foxp3的表达。人类的碎片和CD 4 + CD 25?来自小鼠脾脏的T细胞(1?:β1和1?:α5)在细胞 - 细胞接触或在体外分散,分别为24和72℃。通过流式细胞术评估Tregs的百分比。使用渔民的确切测试和对方差分析进行分析结果。 P? &还0.05被视为统计学意义。结果存在炎症细胞在RET组中存在组织再生,并且富含FoxP3阳性T细胞富集新形成的组织。在体外72℃后,突出促进Treg转化。细胞 - 细胞接触在24小时共培养后发挥了重要作用,而在72℃(p≤0.05)之后也涉及可溶性因子。结论SCAP促进了促炎T细胞的转化为体外Tregs。在RET之后,将Tregs富集在根系中的再生组织周围,这可能产生合适的免疫微环境以分化突出。该研究提供了RET期间组织再生的潜在机制。

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