3 research outputs found
Antibiotic Effects on Microbial Communities Responsible for Greenhouse Gas Emissions
Nitrous oxide (N2O) is a powerful greenhouse gas generated by nitrification and denitrification. The goal of this project is to examine the effects of antibiotics on microbial communities responsible for N2O emissions from terrestrial and aquatic ecosystems. We conducted laboratory and mesocosm experiments in soil samples. Higher N2O production was observed in soils exposed to tetracycline. This was associated with reduction of bacterial denitrifiers abundance and enhanced fungal abundance
Reversal of the NPC Phenotype by START Domain Proteins
Niemann Pick Type C (NPC) disease is a fatal childhood neurological disease caused by mutations in the NPC-1 protein, resulting in cholesterol buildup in the late endosomes. StarD4 and StarD5 are cholesterol binding proteins that play a role in the intracellular cholesterol transport. In this study we overexpress StarD4 and StarD5 in in vitro and in vivo models, and find evidence of amelioration of the NPC phenotype. This study demonstrates that the overexpression of these proteins has the potential to be a therapeutic treatment for NPC disease
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StarD5: an ER stress protein regulates plasma membrane and intracellular cholesterol homeostasis
How plasma membrane (PM) cholesterol is controlled is poorly understood. Ablation of the gene encoding the ER stress steroidogenic acute regulatory-related lipid transfer domain (StarD)5 leads to a decrease in PM cholesterol content, a decrease in cholesterol efflux, and an increase in intracellular neutral lipid accumulation in macrophages, the major cell type that expresses StarD5. ER stress increases StarD5 expression in mouse hepatocytes, which results in an increase in accessible PM cholesterol in WT but not in StarD5-/- hepatocytes. StarD5-/- mice store higher levels of cholesterol and triglycerides, which leads to altered expression of cholesterol-regulated genes. In vitro, a recombinant GST-StarD5 protein transfers cholesterol between synthetic liposomes. StarD5 overexpression leads to a marked increase in PM cholesterol. Phasor analysis of 6-dodecanoyl-2-dimethylaminonaphthalene fluorescence lifetime imaging microscopy data revealed an increase in PM fluidity in StarD5-/- macrophages. Taken together, these studies show that StarD5 is a stress-responsive protein that regulates PM cholesterol and intracellular cholesterol homeostasis