Infected periodontal granulation tissue contains cells expressing embryonic stem cell markers. A pilot study.

V. Ronay, G. Belibasakis, P. Schmidlin, N. Bostancı
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引用次数: 14

Abstract

The commonly practiced removal of granulation tissue during periodontal surgery, aiming to eliminate infection and optimize healing conditions, may also remove progenitor stem cells that could otherwise support periodontal regeneration. The present study aimed to investigate if cells with embryonic stem cell properties are present in periodontal granulation tissue. During the course of flap surgery inflammatory granulation tissue was obtained from four patients and five periodontal defects. Tissues were processed in a collagenase/dispase solution to release the cells. Part of the resulting suspension was processed for bacteriological analysis (IAI PadoTest 4.5), whereas the remaining cell suspension was cultured and passaged once. Upon reaching confluence, total RNA was extracted, followed by cDNA synthesis. PCR was then performed (SYBR Green-based protocols) to measure gene expression levels of Collagen type I, and embryonic stem cell markers Nanog, Oct4, Rex-1 and Sox2. Results are expressed as 2⁻Δ(Ct) values of the target gene, calibrated against a house-keeping gene (GAPDH). A high total bacterial load up to 20.6 ± 11.0×10(6) counts/mg of tissue was found. Collagen type I was strongly expressed, confirming the predominance of mesenchymal/fibroblastic cells. Among the studied embryonic stem cells markers, Nanog was most highly expressed (2.3 ± 1.2), followed by Oct4 (1.1 ± 0.5), Rex-1 (0.6 ± 0.2) and Sox2 (0.3 ± 0.2). This is the first study that demonstrates the presence of cells expressing embryonic stem cell markers among infected granulation tissue. This knowledge needs to be considered when devising future strategies to improve periodontal wound healing and regeneration.
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受感染的牙周肉芽组织含有表达胚胎干细胞标记物的细胞。一项初步研究。
在牙周手术中去除肉芽组织,目的是消除感染和优化愈合条件,也可能去除可以支持牙周再生的祖干细胞。本研究旨在探讨具有胚胎干细胞特性的细胞是否存在于牙周肉芽组织中。在皮瓣手术过程中,有4例患者和5例牙周缺损患者出现炎症性肉芽组织。组织在胶原酶/溶解溶液中处理以释放细胞。部分悬浮液进行细菌学分析(IAI PadoTest 4.5),其余细胞悬浮液进行培养和传代一次。到达汇合处后,提取总RNA,然后进行cDNA合成。然后采用PCR(基于SYBR green的方案)检测I型胶原和胚胎干细胞标记物Nanog、Oct4、Rex-1和Sox2的基因表达水平。结果被表示为目标基因的2 - Δ(Ct)值,根据一个管家基因(GAPDH)进行校准。发现总细菌负荷高达20.6±11.0×10(6)个计数/mg组织。I型胶原蛋白强烈表达,证实了间充质/成纤维细胞的优势。在所研究的胚胎干细胞标记物中,Nanog的表达量最高(2.3±1.2),其次是Oct4(1.1±0.5)、Rex-1(0.6±0.2)和Sox2(0.3±0.2)。这是第一个证明在感染肉芽组织中存在表达胚胎干细胞标记的细胞的研究。在设计未来改善牙周伤口愈合和再生的策略时,需要考虑到这一知识。
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[The state of the art of endodontics]. Patients with oral tumors. Part 1: Prosthetic rehabilitation following tumor resection. Nonsurgical treatment of aggressive periodontitis with photodynamic therapy or systemic antibiotics. Three-month results of a randomized, prospective, controlled clinical study. [Infection after dental intervention. Iatrogenic or general medical cause? Case report]. Patients with oral tumors. Part 1: Prosthetic rehabilitation following tumor resection.
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