Department of Pathology, Tsurumi University School of Dental Medicine, Kanagawa, Japan.
Department of Physical Therapy, Faculty of Rehabilitation, Kyushu Nutrition Welfare University, Fukuoka, Japan; Department of Anatomy, The Nippon Dental University School of Life Dentistry at Niigata, Niigata, Japan.
Differentiation. 2023 Sep-Oct;133:88-97. doi: 10.1016/j.diff.2023.08.001. Epub 2023 Aug 9.
This study investigated the expression of sortilin 1 (SORT1) in cultured human dental pulp-derived stem cells (hDPSCs) and its role in their odontoblastic differentiation. Permanent teeth were extracted from five patients, and the dental pulp was harvested for explant culture. Fluorescence-activated cell sorting was used to analyze the outgrowth of adherent cells and cells that had migrated from the tissue margin. SORT1 expression was detected in hDPSCs simultaneously expressing the mesenchymal stem cell markers CD44 and CD90. The odontoblastic differentiation potential of SORT1-positive hDPSCs was examined via staining for alkaline phosphatase (ALP), an early odontoblastic differentiation marker. ALP staining was more intense in SORT1-positive than in SORT1-negative hDPSCs. Consistently, the expression of mRNA encoding SORT1 and p75, a binding partner of SORT1, increased in SORT1-positive hDPSCs during odontoblastic differentiation. In addition, pro-nerve growth factor (NGF), a ligand for SORT1-p75 co-receptor, promoted ALP expression in SORT1-positive hDPSCs, and the interaction between SORT1 and p75 was detected using a coimmunoprecipitation assay. The function of SORT1 in odontoblastic differentiation was examined via RNA interference using shRNA targeting SORT1. ALP staining intensity in SORT1/shRNA-transfected cells was markedly lower than in control/shRNA-transfected cells. SORT1 knockdown decreased JUN phosphorylation and recruitment of phosphorylated JUN to the ALP promoter. Collectively, these results indicate that SORT1 is involved in the odontoblastic differentiation of hDPSCs through the JUN N-terminal kinases (JNK)/JUN signaling pathway and that the binding of SORT1 and p75 plays an important role in this process.
本研究旨在探讨分选连接蛋白 1(SORT1)在培养的人牙髓干细胞(hDPSCs)中的表达及其在成牙本质细胞分化中的作用。从五名患者中提取恒牙,采集牙髓进行组织块培养。利用荧光激活细胞分选技术分析贴壁细胞和组织边缘迁移细胞的生长情况。SORT1 在同时表达间充质干细胞标志物 CD44 和 CD90 的 hDPSCs 中表达。通过碱性磷酸酶(ALP)染色检测 SORT1 阳性 hDPSCs 的成牙本质细胞分化潜能,ALP 染色在 SORT1 阳性 hDPSCs 中比 SORT1 阴性 hDPSCs 更为强烈。一致地,在 SORT1 阳性 hDPSCs 成牙本质细胞分化过程中,SORT1 和 SORT1 结合伴侣 p75 的 mRNA 表达增加。此外,SORT1-p75 共受体的配体神经生长因子(NGF)促进 SORT1 阳性 hDPSCs 中 ALP 的表达,并通过共免疫沉淀检测到 SORT1 和 p75 之间的相互作用。通过靶向 SORT1 的 shRNA 进行 RNA 干扰来研究 SORT1 在成牙本质细胞分化中的作用。SORT1/shRNA 转染细胞中的 ALP 染色强度明显低于对照/shRNA 转染细胞。SORT1 敲低降低了 JUN 的磷酸化和磷酸化 JUN 向 ALP 启动子的募集。综上所述,这些结果表明 SORT1 通过 JUN N 端激酶(JNK)/JUN 信号通路参与 hDPSCs 的成牙本质细胞分化,SORT1 和 p75 的结合在这一过程中发挥重要作用。