12 research outputs found
Intracellular mannose binding lectin mediates subcellular trafficking of HIV-1 gp120 in neurons.
Heavy Metals Extraction and Analysis in Aquatic Ecosystems with Automated Techniques
The proper choice of a measurement technique is only one step in the development of a successful application. All steps leading up to the measurement are equally important to the sampling and the sample preparation process begins at the point of collection and extends to the measurement step. The sample preparation method used to convert the sample into a form suitable for the measurement step can have a greater effect on the overall accuracy and reability of the results and the measurement itself. Sample preparation is one of the important problems in analytical process. The microwave digestion coupled with ICP MS measurements, for the heavy metals analysis is a very useful tools for the environmental samples
Recommended from our members
Intracellular mannose binding lectin mediates subcellular trafficking of HIV-1 gp120 in neurons.
Human immunodeficiency virus-1 (HIV-1) enters the brain early during infection and leads to severe neuronal damage and central nervous system impairment. HIV-1 envelope glycoprotein 120 (gp120), a neurotoxin, undergoes intracellular trafficking and transport across neurons; however mechanisms of gp120 trafficking in neurons are unclear. Our results show that mannose binding lectin (MBL) that binds to the N-linked mannose residues on gp120, participates in intravesicular packaging of gp120 in neuronal subcellular organelles and also in subcellular trafficking of these vesicles in neuronal cells. Perinuclear MBL:gp120 vesicular complexes were observed and MBL facilitated the subcellular trafficking of gp120 via the endoplasmic reticulum (ER) and Golgi vesicles. The functional carbohydrate recognition domain of MBL was required for perinuclear organization, distribution and subcellular trafficking of MBL:gp120 vesicular complexes. Nocodazole, an agent that depolymerizes the microtubule network, abolished the trafficking of MBL:gp120 vesicles, suggesting that these vesicular complexes were transported along the microtubule network. Live cell imaging confirmed the association of the MBL:gp120 complexes with dynamic subcellular vesicles that underwent trafficking in neuronal soma and along the neurites. Thus, our findings suggest that intracellular MBL mediates subcellular trafficking and transport of viral glycoproteins in a microtubule-dependent mechanism in the neurons
Evaluation of Potable Groundwater Quality Using Environmetrics. The case of Nestos and Strymon River Regions, Northern Greece
In the present study potable water samples were regularly collected from two geographical regions in Northern Greece. The two regions are close to the Nestos and Strymon Rivers. Throughout 2015, samples from 13 sites were collected and analyzed with a frequency of three times per each quarter for the following parameters: chloride, calcium, nitrate, potassium, electric conductivity and total hardness. The main objective of this study was to investigate the effects of the geographical region and seasonal influence on the above parameters regarding the limits of the 98/83/EC Directive. The findings of the Linear Mixed Effects modeling revealed statistically significant main effects of both factors on the examined parameters. © 2021 School of Science, IHU. All rights reserved
Intracellular mannose binding lectin mediates subcellular trafficking of HIV-1 gp120 in neurons
Human immunodeficiency virus -1 (HIV-1) enters the brain early during infection and leads to severe neuronal damage and central nervous system impairment. HIV-1 envelope glycoprotein 120 (gp120), a neurotoxin, undergoes intracellular trafficking and transport across neurons; however mechanisms of gp120 trafficking in neurons are unclear. Our results show that mannose binding lectin (MBL) that binds to the N-linked mannose residues on gp120, participates in intravesicular packaging of gp120 in neuronal subcellular organelles and also in subcellular trafficking of these vesicles in neuronal cells. Perinuclear MBL:gp120 vesicular complexes were observed and MBL facilitated the subcellular trafficking of gp120 via the endoplasmic reticulum (ER) and Golgi vesicles. The functional carbohydrate recognition domain of MBL was required for perinuclear organization, distribution and subcellular trafficking of MBL:gp120 vesicular complexes. Nocodazole, an agent that depolymerizes the microtubule network, abolished the trafficking of MBL:gp120 vesicles, suggesting that these vesicular complexes were transported along the microtubule network. Live cell imaging confirmed the association of the MBL:gp120 complexes with dynamic subcellular vesicles that underwent trafficking in neuronal soma and along the neurites. Thus, our findings suggest that intracellular MBL mediates subcellular trafficking and transport of viral glycoproteins in a microtubule-dependent mechanism in the neurons
Abiraterone and MDV3100 inhibits the proliferation and promotes the apoptosis of prostate cancer cells through mitophagy
Gαs promotes EEA1 endosome maturation and shuts down proliferative signaling through interaction with GIV (Girdin)
Human Immunodeficiency Virus-1/Simian Immunodeficiency Virus Infection Induces Opening of Pannexin-1 Channels Resulting in Neuronal Synaptic Compromise: A Novel Therapeutic Opportunity to Prevent NeuroHIV
In healthy conditions, pannexin-1 (Panx-1) channels are in a close state, but in several pathological conditions, including human immunodeficiency virus-1 (HIV) and NeuroHIV, the channel becomes open. However, the mechanism or contribution of Panx-1 channels to the HIV pathogenesis and NeuroHIV is unknown. To determine the contribution of Panx-1 channels to the pathogenesis of NeuroHIV, we used a well-established model of simian immunodeficiency virus (SIV) infection in macaques (Macaca mulatta) in the presence of and absence of a Panx-1 blocker to later examine the synaptic/axonal compromise induced for the virus. Using Golgi\u27s staining, we demonstrated that SIV infection compromised synaptic and axonal structures, especially in the white matter. Blocking Panx-1 channels after SIV infection prevented the synaptic and axonal compromise induced by the virus, especially by maintaining the more complex synapses. Our data demonstrated that targeting Panx-1 channels can prevent and maybe revert brain synaptic compromise induced by SIV infection