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牙周膜干细胞来源的条件培养基对成骨细胞的影响。

Influence of Periodontal Ligament Stem Cell-Derived Conditioned Medium on Osteoblasts.

作者信息

Novello Solen, Tricot-Doleux Sylvie, Novella Agnès, Pellen-Mussi Pascal, Jeanne Sylvie

机构信息

ISCR (Institut des Sciences Chimiques de Rennes)-UMR 6226, Université de Rennes, 35000 Rennes, France.

Unité de Formation et de Recherche d'Odontologie, Université de Rennes, 35000 Rennes, France.

出版信息

Pharmaceutics. 2022 Mar 28;14(4):729. doi: 10.3390/pharmaceutics14040729.

Abstract

Mesenchymal stem cells (MSC) are involved in the regeneration of various missing or compromised periodontal tissues, including bone. MSC-derived conditioned medium (CM) has recently been explored as a favorable surrogate for stem cell therapy, as it is capable of producing comparable therapeutic effects. This study aimed to evaluate the influence of periodontal ligament stem cells (PDLSC)-CM on osteoblasts (OB) and its potential as a therapeutic tool for periodontal regeneration. Human PDLSC were isolated and characterized, and CM from these cells was collected. The presence of exosomes in the culture supernatant was observed by immunofluorescence and by transmission electron microscopy. CM was added to a cultured osteoblastic cell line (Saos-2 cells) and viability (MTT assay) and gene expression analysis (real-time PCR) were examined. A cell line derived from the periodontal ligament and showing all the characteristics of MSC was successfully isolated and characterized. The addition of PDLSC-CM to Saos-2 cells led to an enhancement of their proliferation and an increased expression of some osteoblastic differentiation markers, but this differentiation was not complete. Saos-2 cells were involved in the initial inflammation process by releasing IL-6 and activating COX2. The effects of PDLSC-CM on Saos-2 appear to arise from a cumulative effect of different effective components rather than a few factors present at high levels.

摘要

间充质干细胞(MSC)参与包括骨组织在内的各种缺失或受损牙周组织的再生。间充质干细胞来源的条件培养基(CM)最近被视为干细胞治疗的一种理想替代物,因为它能够产生类似的治疗效果。本研究旨在评估牙周膜干细胞(PDLSC)-CM对成骨细胞(OB)的影响及其作为牙周再生治疗工具的潜力。分离并鉴定人牙周膜干细胞,收集这些细胞的条件培养基。通过免疫荧光和透射电子显微镜观察培养上清液中外泌体的存在。将条件培养基添加到培养的成骨细胞系(Saos-2细胞)中,检测细胞活力(MTT法)和基因表达分析(实时PCR)。成功分离并鉴定了一种源自牙周膜且具有间充质干细胞所有特征的细胞系。将牙周膜干细胞条件培养基添加到Saos-2细胞中可增强其增殖,并增加一些成骨细胞分化标志物的表达,但这种分化并不完全。Saos-2细胞通过释放白细胞介素-6和激活环氧化酶2参与初始炎症过程。牙周膜干细胞条件培养基对Saos-2细胞的影响似乎源于不同有效成分的累积效应,而非少数高水平存在的因子的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87e3/9028528/b890ac35cc06/pharmaceutics-14-00729-g001.jpg

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