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1.
J Invertebr Pathol ; 201: 107990, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37690679

ABSTRACT

Our study aimed to examine whether there are differences in the proliferation trend of microsporidia in mosquito larvae of the same genus (Culex spp.). DNA-barcoding and quantitative analyses were used to determine microsporidian rDNA copies in 'early' (L1 + L2) and 'late' (L3 + L4) Culex larvae in a natural population. In the study area, C. pipiens and C. torrentium larvae were infected by 'Microsporidium' sp. PL03 at similar levels. Infection by this microsporidian species probably elicits a notable immune response in C. pipiens, whereas in C. torrentium, it may evade or suppress the host immune response.


Subject(s)
Culex , Microsporidia, Unclassified , Microsporidia , Animals , Larva/genetics , Microsporidia/genetics , Cell Proliferation
2.
Mitochondrion ; 28: 38-48, 2016 05.
Article in English | MEDLINE | ID: mdl-26994639

ABSTRACT

It has been previously demonstrated that cytoprotective activity displayed by minocycline in the case of the yeast Saccharomyces cerevisiae cells pretreated with H2O2 requires the presence of functional VDAC (YVDAC1). Thus, we decided to transform YVDAC1-depleted yeast cells (Δpor1 cells) with plasmids expressing human VDAC isoforms (HVDAC1, HVDAC2, HVDAC3) to estimate their involvement in the minocycline cytoprotective effect. We observed that only expression of HVDAC3 in Δpor1 cells provided minocycline-mediated cytoprotection against H2O2 although all human isoforms are functional in Δpor1 cells. The observation appears to be important for on-going discussion concerning VDAC isoform roles in mitochondria and cell functioning.


Subject(s)
Antioxidants/metabolism , Antioxidants/pharmacology , Cytoprotection , Minocycline/metabolism , Minocycline/pharmacology , Protein Isoforms/metabolism , Voltage-Dependent Anion Channels/metabolism , Humans , Hydrogen Peroxide/toxicity , Protein Binding , Protein Isoforms/genetics , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Saccharomyces cerevisiae/drug effects , Voltage-Dependent Anion Channels/genetics
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