Immunomodulatory/inflammatory effects of geopropolis produced by Melipona fasciculata Smith in combination with doxorubicin on THP-1 cells
cell markers
Time Factors
Cell Survival
610
immunomodulation
Monocytes
Propolis
03 medical and health sciences
0302 clinical medicine
Cell Line, Tumor
Antineoplastic Combined Chemotherapy Protocols
Animals
Humans
geopropolis
Inflammation
chemotherapeutic agent
Dose-Response Relationship, Drug
Interleukin-6
Macrophages
THP-1 cells
HLA-DR Antigens
Bees
Toll-Like Receptor 2
3. Good health
Toll-Like Receptor 4
Doxorubicin
B7-1 Antigen
Inflammation Mediators
Biomarkers
DOI:
10.1111/jphp.12649
Publication Date:
2016-10-17T08:12:39Z
AUTHORS (8)
ABSTRACT
Abstract
Objectives
Geopropolis (GEO) in combination with doxorubicin (DOX) reduced HEp-2 cells viability compared to GEO and DOX alone. A possible effect of this combination on the innate immunity could take place, and its effects were analysed on THP-1 cell – a human leukaemia monocytic cell line used as a model to study monocyte activity and macrophage activity, assessing cell viability, expression of cell markers and cytokine production.
Methods
THP-1 cells were incubated with GEO, DOX and their combination. Cell viability was assessed by MTT assay, cell markers expression by flow cytometry and cytokine production by ELISA.
Key findings
GEO + DOX did not affect cell viability. GEO alone or in combination increased TLR-4 and CD80 but not HLA-DR and TLR-2 expression. GEO stimulated TNF-α production while DOX alone or in combination did not affect it. GEO alone or in combination inhibited IL-6 production.
Conclusions
GEO exerted a pro-inflammatory profile by increasing TLR-4 and CD80 expression and TNF-α production, favouring the activation of the immune/inflammatory response. GEO + DOX did not affect cell viability and presented an immunomodulatory action. Lower concentrations of DOX combined to GEO could be used in cancer patients, avoiding side effects and benefiting from the biological properties of GEO.
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