Tian Zhiwei, Zhao Zhongqi, Rausch Marco Aoqi, Behm Christian, Tur Dino, Shokoohi-Tabrizi Hassan Ali, Andrukhov Oleh, Rausch-Fan Xiaohui
Competence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria.
Clinical Division of Orthodontics, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria.
Int J Mol Sci. 2025 Jan 15;26(2):672. doi: 10.3390/ijms26020672.
Over the past few years, biomaterial-based periodontal tissue engineering has gained popularity. An ideal biomaterial for treating periodontal defects is expected to stimulate periodontal-derived cells, allowing them to contribute most efficiently to tissue reconstruction. The present study focuses on evaluating the in vitro behavior of human periodontal ligament-derived stromal cells (hPDL-MSCs) when cultured on gelatin/Polycaprolactone prototype (GPP) and volume-stable collagen matrix (VSCM). Cells were cultured onto the GPP, VSCM, or tissue culture plate (TCP) for 3, 7, and 14 days. Cell morphology, adhesion, proliferation/viability, the gene expression of Collagen type I, alpha1 (COL1A1), Vascular endothelial growth factor A (VEGF-A), Periostin (POSTN), Cementum protein 1 (CEMP1), Cementum attachment protein (CAP), Interleukin 8 (IL-8) and Osteocalcin (OCN), and the levels of VEGF-A and IL-8 proteins were investigated. hPDL-MSCs attached to both biomaterials exhibited a different morphology compared to TCP. GPP exhibited stronger capabilities in enhancing cell viability and metabolic activity compared to VSCM. In most cases, the expression of all investigated genes, except POSTN, was stimulated by both materials, with GPP having a superior effect on COL1A1 and VEGF-A, and VSCM on OCN. The IL-8 protein production was slightly higher in cells grown on VSCM. GPP also exhibited the ability to absorb VEGF-A protein. The gene expression of POSTN was promoted by GPP and slightly suppressed by VSCM. In summary, our findings indicate that GPP electrospun nanofibers effectively promote the functional performance of PDLSCs in periodontal regeneration, particularly in the periodontal ligament and cementum compartment.
在过去几年中,基于生物材料的牙周组织工程越来越受欢迎。一种用于治疗牙周缺损的理想生物材料有望刺激牙周来源的细胞,使其最有效地促进组织重建。本研究重点评估人牙周膜来源的基质细胞(hPDL-MSCs)在明胶/聚己内酯原型(GPP)和体积稳定胶原基质(VSCM)上培养时的体外行为。将细胞接种到GPP、VSCM或组织培养板(TCP)上培养3天、7天和14天。研究了细胞形态、黏附、增殖/活力、I型胶原α1(COL1A1)、血管内皮生长因子A(VEGF-A)、骨膜蛋白(POSTN)、牙骨质蛋白1(CEMP1)、牙骨质附着蛋白(CAP)、白细胞介素8(IL-8)和骨钙素(OCN)的基因表达,以及VEGF-A和IL-8蛋白的水平。与TCP相比,附着在两种生物材料上的hPDL-MSCs表现出不同的形态。与VSCM相比,GPP在增强细胞活力和代谢活性方面表现出更强的能力。在大多数情况下,除POSTN外,两种材料均刺激所有研究基因的表达,GPP对COL1A1和VEGF-A的作用更优,VSCM对OCN的作用更优。在VSCM上生长的细胞中IL-8蛋白产量略高。GPP还表现出吸收VEGF-A蛋白的能力。GPP促进POSTN的基因表达,VSCM则轻微抑制其表达。总之,我们的研究结果表明,GPP电纺纳米纤维有效地促进了PDLSCs在牙周再生中的功能表现,特别是在牙周膜和牙骨质区域。