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Toll-like receptor 2 and dectin-1 function as promising biomarker for infection. | LitMetric

Toll-like receptor 2 and dectin-1 function as promising biomarker for infection.

Exp Ther Med

Department of Respiratory and Critical Care Medicine, Jinling Hospital, Nanjing Clinical College, The Second Military Medical University, Nanjing, Jiangsu 210002, P.R. China.

Published: October 2017

In recent years, along with the wide application of organ transplantation and immunosuppressive agents, as well as the abuse of broad spectrum antibiotics, the incidence of invasive fungal infections has been increasing gradually. The present study aimed to identify novel biomarkers in cells infected with . Human umbilical vein endothelial cells (HUVECs) were infected with and then harvested at different time-points (0, 1, 2, 4 and 6 h). The expression Toll-like receptor 2 (TLR2) and dectin-1 expression were examined using flow cytometry and western blotting, and fluorescence-based microscopy was used to evaluate their distribution. The results indicated that TLR2 and dectin-1 protein levels were localized on the surface of HUVECs, and that dectin-1 was distributed on HUVEC membranes as observed under confocal microscope. Immunofluorescence assay result revealed that the optical intensity of dectin-1 in the -infected group was significantly increased at 0, 1 and 2 h compared with the control group (P<0.05). However, the optical intensity of TLR2 in the -infected group was markedly decreased between 0 and 6 h, as compared with the control group (P<0.05). Western blot analysis indicated that dectin-1 expression was significantly increased and TLR2 expression was significantly decreased at 0, 1 and 2 h post infection in the -infected group compared with the control group. Furthermore, the expression of TLR2 was also negatively correlated with the concentration of . In conclusion, upon infection of cells with , TLR2 and dectin-1 expression levels were significantly altered. Therefore, TLR2 and dectin-1 levels may function as promising biomarkers for the treatment or diagnosis of infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639428PMC
http://dx.doi.org/10.3892/etm.2017.5000DOI Listing

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