Cellular and Molecular Response of Macrophages THP-1 during Co-Culture with Inactive Trichophyton rubrum Conidia.
Gabriela Gonzalez SeguraBruna Aline CantelliKamila PeronniPablo Rodrigo SanchesTatiana Takahasi KomotoElen RizziRene Oliveira BeleboniWilson Araújo da Silva JuniorNilce Maria Martinez-RossiMozart MarinsAna Lucia FachinPublished in: Journal of fungi (Basel, Switzerland) (2020)
Trichophyton rubrum is causing an increasing number of invasive infections, especially in immunocompromised and diabetic patients. The fungal invasive infectious process is complex and has not yet been fully elucidated. Therefore, this study aimed to understand the cellular and molecular mechanisms during the interaction of macrophages and T. rubrum. For this purpose, we used a co-culture of previously germinated and heat-inactivated T. rubrum conidia placed in contact with human macrophages cell line THP-1 for 24 h. This interaction led to a higher level of release of interleukins IL-6, IL-2, nuclear factor kappa beta (NF-κB) and an increase in reactive oxygen species (ROS) production, demonstrating the cellular defense by macrophages against dead fungal elements. Cell viability assays showed that 70% of macrophages remained viable during co-culture. Human microRNA expression is involved in fungal infection and may modulate the immune response. Thus, the macrophage expression profile of microRNAs during co-culture revealed the modulation of 83 microRNAs, with repression of 33 microRNAs and induction of 50 microRNAs. These data were analyzed using bioinformatics analysis programs and the modulation of the expression of some microRNAs was validated by qRT-PCR. In silico analysis showed that the target genes of these microRNAs are related to the inflammatory response, oxidative stress, apoptosis, drug resistance, and cell proliferation.
Keyphrases
- nuclear factor
- oxidative stress
- inflammatory response
- toll like receptor
- reactive oxygen species
- endothelial cells
- cell proliferation
- immune response
- bioinformatics analysis
- poor prognosis
- dna damage
- cell death
- public health
- induced pluripotent stem cells
- signaling pathway
- pi k akt
- lps induced
- binding protein
- intensive care unit
- electronic health record
- adipose tissue
- endoplasmic reticulum stress
- single molecule
- transcription factor
- lipopolysaccharide induced
- diabetic rats
- ischemia reperfusion injury
- heat stress
- molecular docking
- induced apoptosis