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Francisco R.M. Laurindo

Researcher at University of São Paulo

Publications -  214
Citations -  7762

Francisco R.M. Laurindo is an academic researcher from University of São Paulo. The author has contributed to research in topics: Protein disulfide-isomerase & Oxidative stress. The author has an hindex of 44, co-authored 198 publications receiving 6895 citations.

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Mechanisms and implications of reactive oxygen species generation during the unfolded protein response: roles of endoplasmic reticulum oxidoreductases, mitochondrial electron transport, and NADPH oxidase.

TL;DR: Evidence suggests that ROS production and oxidative stress are not only coincidental to ER stress, but are integral UPR components, being triggered by distinct types of ER stressors and contributing to support proapoptotic, as well as proadaptive UPR signaling.
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Blood Meal-Derived Heme Decreases ROS Levels in the Midgut of Aedes aegypti and Allows Proliferation of Intestinal Microbiota

TL;DR: It is proposed that a controlled decrease in ROS levels in the midgut of Aedes aegypti is an adaptation to compensate for the ingestion of heme, a pro-oxidant molecule released in large amounts upon hemoglobin degradation, which would represent a burden to the insect.
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Regulation of NAD(P)H Oxidase by Associated Protein Disulfide Isomerase in Vascular Smooth Muscle Cells

TL;DR: The results suggest that PDI closely associates with NAD(P)H oxidase and acts as a novel redox-sensitive regulatory protein of such enzyme complex, potentially affecting subunit traffic/assembling.
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Vascular free radical release. Ex vivo and in vivo evidence for a flow-dependent endothelial mechanism.

TL;DR: Increases in blood flow trigger vascular free radical generation; such a response seems to involve endothelium-derived superoxide radicals unrelated to cyclooxygenase or nitric oxide synthetase activities.
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Protein disulfide isomerase in redox cell signaling and homeostasis.

TL;DR: Redox effects of protein disulfide isomerase (PDI), a thioredoxin superfamily oxidoreductase from the endoplasmic reticulum (ER), are discussed, suggesting a convergence between PDI and Nox family NADPH oxidases.