Department of Conservative Dentistry and Periodontology, University Hospital, Ludwig-Maximilians-University, LMU Munich, Goethestr. 70, 80336, Munich, Germany.
Clin Oral Investig. 2023 Oct;27(10):5905-5911. doi: 10.1007/s00784-023-05202-z. Epub 2023 Aug 17.
While HA is present naturally in periodontal tissues, its molecular weight can vary widely in vivo. The objective of this study was to directly compare the biological reactions of periodontal ligament cells to four distinct molecular weights of hyaluronic acid (HA).
Immortalized human periodontal ligament cells (PDL-hTERT) were cultured for 21 days in culture medium alone (control) or enriched with osteogenic supplements (OS group). Other 4 experimental groups were cultured in OS medium with the addition of HA with different molecular weights (HMW, MMW, LMW, and ULMW). The cell morphology was examined daily. WST1 assays were performed to evaluate metabolic activity. Von Kossa staining and calcium deposition assay were used to analyze osteogenic differentiation and mineralization.
Cell morphology remained unaltered in all groups. Cells stimulated with OS alone or with the addition of hyaluronan showed all the typical microscopic appearance of osteogenic differentiation. Metabolic activity increased in all groups over time. Hyaluronan stimulated greater metabolic activity than the control group, with LMW HA and MMW HA showing the most significant increase. All groups showed mineral deposits and calcium deposition after 21 days of stimulation.
Our results suggest that hyaluronan can promote metabolic activity and mineralization of PDL-hTERT cells, with LMW HA being the most effective.
These results shed light on how the various molecular weight fractions of HA promote tissue regeneration and repair, as well as help to identify an optimal molecular weight range for this application in periodontal tissues.
虽然 HA 天然存在于牙周组织中,但它的分子量在体内有很大的变化。本研究的目的是直接比较牙周膜细胞对四种不同分子量的透明质酸(HA)的生物学反应。
永生化人牙周膜细胞(PDL-hTERT)在培养基中培养 21 天(对照组)或在富含成骨补充剂的培养基中培养(OS 组)。其他 4 个实验组在 OS 培养基中加入不同分子量的 HA(HMW、MMW、LMW 和 ULMW)进行培养。每天观察细胞形态。使用 WST1 分析评估代谢活性。Von Kossa 染色和钙沉积分析用于分析成骨分化和矿化。
所有组的细胞形态均未改变。单独用 OS 刺激或添加透明质酸刺激的细胞显示出所有典型的成骨分化的微观外观。随着时间的推移,所有组的代谢活性均增加。透明质酸刺激的代谢活性高于对照组,其中 LMW HA 和 MMW HA 的增加最为显著。所有组在刺激 21 天后均显示出矿化沉积物和钙沉积。
我们的结果表明,透明质酸可以促进 PDL-hTERT 细胞的代谢活性和矿化,其中 LMW HA 最为有效。
这些结果揭示了不同分子量的 HA 如何促进组织再生和修复,并有助于确定在牙周组织中应用的最佳分子量范围。