State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China; National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China; Department of Orthodontics, West China School of Stomatology, Sichuan University, Chengdu 610041, PR China.
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China; National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China; Department of Pediatric Dentistry, West China Hospital of Stomatology, Sichuan University, Chengdu, PR China.
Arch Oral Biol. 2018 Oct;94:1-9. doi: 10.1016/j.archoralbio.2018.06.014. Epub 2018 Jun 18.
The role of Hertwig's epithelial root sheath (HERS) cells in periodontal formation has been controversial. This study aimed to further clarify whether HERS cells participate in formation of the periodontium, and the necessity of HERS cells in differentiation of dental follicle cells (DFCs) for periodontal regeneration.
HERS cells and DFCs were isolated and identified from post-natal 7-day Sprauge-Dawley rats. In vitro, direct co-culture of HERS cells and DFCs as well as the individual culture of HERS and DFCs were performed and followed by alizarin red staining and the quantitative real-time polymerase chain reaction analysis. For in vivo evaluation, the inactivated dentin matrix (iTDM) was fabricated. HERS cells and DFCs were seeded in combination or alone on iTDM and then transplanted into the rat omentum. Scanning electron microscope and further histological analysis were carried out.
In vitro, mineral-like nodules were found in the culture of HERS cells alone or HERS + DFCs either by alizarin red staining or scanning electronic microscope. The mineralization and fiber-forming relevant mRNA expressions, such as bone sialoprotein, osteopontin, collagen I and collagen III in HERS + DFCs were significantly higher than that of the HERS or DFCs alone group. After transplantation in vivo, cementum and periodontal ligament-like tissues were formed in groups of HERS + DFCs and HERS alone, while no evident hard tissues and attached fibers were found in DFCs alone.
Hertwig's epithelial root sheath cells directly participate in the formation of the periodontium, and they are essential for the differentiation of dental follicle cells to form periodontal structures. The combination use of Hertwig's epithelial root sheath cells and dental follicle cells is a promising approach for periodontal regeneration.
赫特威氏上皮根鞘(HERS)细胞在牙周形成中的作用一直存在争议。本研究旨在进一步阐明 HERS 细胞是否参与牙周组织的形成,以及 HERS 细胞在牙囊细胞(DFCs)分化为牙周再生所必需的牙周结构中的作用。
从出生后 7 天的 Sprauge-Dawley 大鼠中分离和鉴定 HERS 细胞和 DFCs。在体外,进行 HERS 细胞和 DFCs 的直接共培养以及 HERS 和 DFCs 的单独培养,然后进行茜素红染色和实时定量聚合酶链反应分析。为了进行体内评估,制备了灭活牙本质基质(iTDM)。将 HERS 细胞和 DFCs 组合或单独接种在 iTDM 上,然后移植到大鼠大网膜中。进行扫描电子显微镜和进一步的组织学分析。
在体外,单独培养 HERS 细胞或 HERS+DFCs 均可通过茜素红染色或扫描电子显微镜观察到类矿化结节。HERS+DFCs 的矿化和纤维形成相关 mRNA 表达,如骨涎蛋白、骨桥蛋白、I 型胶原和 III 型胶原,明显高于 HERS 或 DFCs 单独培养组。体内移植后,在 HERS+DFCs 和 HERS 单独培养组中形成了牙骨质和牙周韧带样组织,而在 DFCs 单独培养组中则没有明显的硬组织和附着纤维。
赫特威氏上皮根鞘细胞直接参与牙周组织的形成,并且是牙囊细胞分化为牙周结构所必需的。赫特威氏上皮根鞘细胞和牙囊细胞的联合使用是牙周再生的一种有前途的方法。