Cell Responses to Conditioned Media Produced by Patient‐Matched Stem Cells Derived From Healthy and Inflamed Periodontal Ligament Tissues

牙周纤维 牙周膜干细胞 干细胞 医学 牙科 化学 细胞生物学 生物 生物化学 碱性磷酸酶
作者
Yu Xia,Hao‐Ning Tang,Rui‐Xin Wu,Yang Yu,Li‐Na Gao,Fa‐Ming Chen
出处
期刊:Journal of Periodontology [Wiley]
卷期号:87 (5): e53-63 被引量:31
标识
DOI:10.1902/jop.2015.150462
摘要

BACKGROUND: Periodontal ligament stem cells (PDLSCs) derived from clinically compromised teeth with periodontitis are considered a readily accessible cell source, but their impaired stem cell functionalities, as observed in various in vitro and in vivo models, necessitate further investigation of these inflamed cells before their translation into therapeutic applications. In this study, the effects of conditioned media (CM) produced by stem cells derived from human healthy periodontal ligament tissues (H-PDLSCs) or inflamed periodontal ligament tissues (I-PDLSCs), referred to as H-CM and I-CM, respectively, on the biologic properties of H-PDLSCs and I-PDLSCs from the same donor are compared to explore the extent to which inflamed cells can be rescued by their extrinsic environment (i.e., by H-CM). METHODS: H-CM and I-CM were prepared from in vitro cell cultures, and the cellular responses of H-PDLSCs and I-PDLSCs to patient-matched H-CM and I-CM were investigated in terms of colony-forming ability, cell proliferation, and adipogenic/osteogenic differentiation. RESULTS: In H-CM and I-CM, H-PDLSCs and I-PDLSCs exhibited similar adipogenic potential. However, when incubated in I-CM, both cell types demonstrated an increased capacity to proliferate but a decreased capacity to differentiate into osteoblasts. Significantly, the impaired osteogenic differentiation of I-PDLSCs was partially rescued by incubation in H-CM under osteo-inducing conditions. CONCLUSION: The CM of patient-matched H-PDLSCs and I-PDLSCs differed, and the impaired osteogenic differentiation of inflamed stem cells had the potential to be rescued, at least partially, for therapeutic use via changing the cell culture microenvironment in vitro.

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