Lee Hyung-Joo, Jeon Mijeong, Kim Young-Han, Kim Seong-Oh, Lee Ko Eun
Department of Pediatric Dentistry, Yonsei University College of Dentistry, Seoul, Republic of Korea.
Oral Science Research Center, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
J Dent Sci. 2023 Jan;18(1):211-219. doi: 10.1016/j.jds.2022.06.005. Epub 2022 Jun 29.
BACKGROUND/PURPOSE: Due to their regenerative potential, periodontal ligament (PDL) and umbilical cord (UBC) tissues are an attractive potential mesenchymal stem cells (MSCs) source. This study compared the expression patterns of genes related to stemness between fresh PDL and UBC tissues.
PDL tissues were collected from 38 permanent premolars extracted for orthodontic purposes, and UBC tissues were obtained from three newborns. Each sample was immediately frozen to prevent RNA degradation. cDNA microarray analysis, quantitative real-time polymerase chain reaction (PCR), and immunohistochemical staining were performed. Gene expression patterns associated with dental stemness (DS) and induced pluripotent stemness (iPS) were compared between PDL and UBC tissues.
In the cDNA microarray analyses, the expressions of most iPS genes were greater in the PDL than in the UBC. Meanwhile, the expressions of most DS genes were greater in the UBC than in the PDL. Quantitative real-time PCR analyses showed that the expression levels of matrix metallopeptidase 13 (MMP13), ADAM metallopeptidase domain 22 (ADAM22), vascular cell adhesion protein 1 (VCAM1), and kruppel-like factor 4 (KLF4) genes were greater in the PDL than in the UBC, while the expressions of melanoma cell adhesion molecule (MCAM) and activated leukocyte cell adhesion molecule (ALCAM) were greater in the UBC than in the PDL.
These results suggest that UBC and PDL tissues showed slightly different expression patterns of genes related to stemness, which warrants further investigation to use these tissues for future regeneration and implantation therapies.
背景/目的:由于牙周膜(PDL)和脐带(UBC)组织具有再生潜力,它们是一种有吸引力的潜在间充质干细胞(MSCs)来源。本研究比较了新鲜PDL和UBC组织中与干性相关基因的表达模式。
从38颗因正畸拔除的恒牙前磨牙中收集PDL组织,从3名新生儿中获取UBC组织。每个样本立即冷冻以防止RNA降解。进行了cDNA微阵列分析、定量实时聚合酶链反应(PCR)和免疫组织化学染色。比较了PDL和UBC组织中与牙源性干性(DS)和诱导多能性干性(iPS)相关的基因表达模式。
在cDNA微阵列分析中,大多数iPS基因在PDL中的表达高于UBC。同时,大多数DS基因在UBC中的表达高于PDL。定量实时PCR分析表明,基质金属蛋白酶13(MMP13)、ADAM金属蛋白酶结构域22(ADAM22)、血管细胞粘附蛋白1(VCAM1)和克鲁ppel样因子4(KLF4)基因在PDL中的表达高于UBC,而黑素瘤细胞粘附分子(MCAM)和活化白细胞细胞粘附分子(ALCAM)在UBC中的表达高于PDL。
这些结果表明,UBC和PDL组织显示出与干性相关基因的表达模式略有不同,这值得进一步研究,以便将这些组织用于未来的再生和植入治疗。