Immune responses of human dental pulp stem cells in lipopolysaccharide-induced microenvironment

被引:50
作者
Bindal, Priyadarshini [1 ]
Ramasamy, Thamil Selvee [2 ]
Abu Kasim, Noor Hayaty [1 ]
Gnanasegaran, Nareshwaran [1 ]
Chai, Wen Lin [1 ]
机构
[1] Univ Malaya, Dept Restorat Dent, Fac Dent, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Dept Mol Med, Fac Med, Kuala Lumpur 50603, Malaysia
关键词
cytokines; interleukins; mesenchymal stem cells; permanent tooth; SUBSTANCE-P; IN-VITRO; INFLAMMATION; INTERLEUKIN-8; TNF; EXPRESSION; MIGRATION; CARIES; LPS;
D O I
10.1002/cbin.10938
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
This study aimed to investigate the effect of inflammatory stimuli on dental pulp stem cells (DPSCs) by assessing their proliferation and expression of genes as well as proteins in lipopolysaccharide (LPS)-induced microenvironment (iDPSCs). DPSCs were first characterized for their mesenchymal properties prior to challenging them with a series of LPS concentrations from 12 to 72h. Following to this, their proliferation and inflammatory based genes as well as protein expression were assessed. iDPSCs had demonstrated significant expression of mesenchymal markers. Upon exposure to LPS, the viability dropped distinctly with increasing concentration, as compared to control (P<0.05). The expression of pro-inflammatory genes such as interleukin 6, interleukin 8 were augmented with exposure to LPS (P<0.05). Similarly, cytokines like tumour necrosis factor (TNF) and interleukin 1 had increased in dose dependant manner upon LPS exposure (P<0.05). Our results suggest that LPS concentration between 1 and 2g/mL demonstrated inflammation induction in DPSCs that may simulate inflamed microenvironment of dental pulp in clinical scenario. Thus, optimizing iDPSCs secretome profile could be a promising approach to test various regenerative protocols in inflamed microenvironment.
引用
收藏
页码:832 / 840
页数:9
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