Publications by authors named "Forte E"

Down Syndrome (DS) is a genetic disorder caused by the presence of an extra copy of chromosome 21, and leading to various developmental and cognitive defects. A critical feature of DS is the occurrence of oxidative distress particularly in the brain, which exacerbates neurodevelopmental processes. Mitochondria play a crucial role in cell energy metabolism and their impairment is one of the major causes of oxidative distress in several pathologies.

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Multi-technique integrated surveys were carried out to investigate brine characteristics, connectivity and flow patterns in the Boulder Clay Glacier area, Victoria Land, East Antarctica. Specifically, electromagnetic geophysical surveys focused mainly on Ground Penetrating Radar (GPR) and integrated by Frequency Domain induction, not only demonstrated the presence of brines in the subsurface, but also allowed to image several structures and glaciological elements. Chemical analyses suggested the origin and differentiation of the brines, providing evidence for interconnected pathways.

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  • - Cirrhosis affects 2 to 5 million Americans, with most patients experiencing compensated cirrhosis, yet many can develop serious complications that severely shorten life expectancy.
  • - Identifying high-risk patients with compensated cirrhosis is crucial for improving their care and directing them to specialty treatment, as not all patients receive this level of care.
  • - This pilot study identified 209 differentially expressed proteoforms in the plasma of cirrhosis patients at various stages, highlighting potential biomarkers that could help in early diagnosis and risk assessment.
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Recent studies discovered the prominent presence of anti-nephrin autoantibodies in minimal change disease, steroid-sensitive nephrotic syndrome and/or post-transplant recurrent focal segmental glomerulosclerosis (FSGS). However, widely different, and often unconventional autoantibody detection methods were used among these studies, making it challenging to assess the pathogenic role for the antibodies. Here we examined methods of conventional ELISA, magnetic on-beads ELISA, immunoprecipitation-immunoblotting (IP-IB), and cell- and tissue-based antibody assays with 127 plasma samples of kidney and non-kidney diseases.

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  • Organ transplant recipients on immunosuppressants have a weakened ability to respond to infections, including SARS-CoV-2, but their antibody responses may still be effective.
  • A new mass spectrometry technique called Ig-MS was used to compare immune responses to COVID-19 between transplant recipients and immunocompetent controls at a single point and over a month after diagnosis.
  • The study found no significant differences in antibody characteristics like titer, clonality, or glycan composition between the two groups, suggesting that the immune response evolution in transplant recipients resembles that of immunocompetent individuals.
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Charge detection mass spectrometry (CDMS) is a well-established technique that provides direct mass spectral outputs regardless of analyte heterogeneity or molecular weight. Over the past few years, it has been demonstrated that CDMS can be multiplexed on Orbitrap analyzers utilizing an integrated approach termed individual ion mass spectrometry (IMS). To further increase adaptability, robustness, and throughput of this technique, here, we present a method that utilizes numerous integrated equipment components including a Kingfisher system, SampleStream platform, and Q Exactive mass spectrometer to provide a fully automated workflow for immunoprecipitation, sample preparation, injection, and subsequent IMS acquisition.

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  • Amyloidosis is linked to chronic diseases, and this study investigates its role as a complication following a myocardial infarction (MI), highlighting the need for further understanding.
  • The research utilized mouse models to reveal that macrophages produce excessive amounts of Serum Amyloid A 3 (SAA3) protein after MI due to communication with activated mesenchymal stromal cells (MSC), which alter their behavior in response to heart injury.
  • Results indicate that the aggregation of SAA3 proteins into amyloid deposits makes the heart scar tissue stiffer, reducing heart function post-MI; however, targeting SAA3 aggregation with a specialized D-peptide shows potential for improving heart health after an MI.
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Scarcity of high-quality organs, suboptimal organ quality assessment, unsatisfactory pre-implantation procedures, and poor long-term organ and patient survival are the main challenges currently faced by the solid organ transplant (SOT) field. New biomarkers for assessing graft quality pre-implantation, detecting, and predicting graft injury, rejection, dysfunction, and survival are critical to provide clinicians with invaluable prediction tools and guidance for personalized patients' treatment. Additionally, new therapeutic targets are also needed to reduce injury and rejection and improve transplant outcomes.

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  • - Cirrhosis affects 2-5 million Americans, with many patients asymptomatic until they experience serious complications that can drastically reduce life expectancy from 12 years to less than 2.
  • - Identifying high-risk patients with compensated cirrhosis is crucial for optimizing care, as not all patients can access specialized treatment.
  • - A study using Top-down Proteomics identified 209 differentially expressed proteoforms in patients at different stages of cirrhosis, revealing potential biomarkers for disease progression and informing future diagnostic and monitoring strategies.
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  • Brain insulin resistance connects energy metabolism failure to cognitive decline in type 2 diabetes and Alzheimer's disease, but the early changes leading to insulin resistance are not well understood.
  • Abnormal levels of biliverdin reductase-A (BVR-A) are found in both conditions, linked to insulin resistance and affecting insulin signaling and energy production in the brain.
  • The study reveals that lower BVR-A disrupts insulin response and mitochondrial function, highlighting its importance for potential therapeutic targets to combat brain insulin resistance and neurodegeneration.
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  • Chronic immunopathology plays a significant role in developing heart failure after a myocardial infarction, with both T and B cells involved in the immune response in the heart.
  • Researchers analyzed T and B cell populations from existing RNA-sequencing datasets to understand their roles in post-MI immunopathology.
  • Following a myocardial infarction, T cells become pro-inflammatory, while B cells enhance activation markers and collagen production, indicating their involvement in both immediate healing and ongoing inflammation that contributes to heart failure.
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Hydrogen sulfide (HS) and nitric oxide (NO) are long-known inhibitors of terminal oxidases in the respiratory chain. Yet, they exert pivotal signaling roles in physiological processes, and in several bacterial pathogens have been reported to confer resistance against oxidative stress, host immune responses, and antibiotics. , an opportunistic pathogen causing life-threatening infections that are difficult to eradicate, has a highly branched respiratory chain including four terminal oxidases of the haem-copper type (, , , and ) and one oxidase of the -type (cyanide-insensitive oxidase, CIO).

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Aim: Recently, the relationship between diabetes and mental health has been widely studied. With the advent of continuous glucose monitoring (CGM), some researchers have been interested in exploring the association between glucose-related metrics and psychological aspects. These studies have primarily relied on self-report questionnaires which present some limitations.

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Hydrogen sulfide (HS) has been proposed to protect bacteria from antibiotics, pointing to HS-producing enzymes as possible targets for the development of antibiotic adjuvants. Here, MIC assays performed with mutants producing altered HS levels demonstrate that HS does not affect antibiotic resistance in this bacterium. Moreover, correlation analyses in a large collection of cystic fibrosis isolates argue against the protective role of HS from antibiotic activity during chronic lung infection.

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Myocarditis has emerged as an immune-related adverse event of immune checkpoint inhibitor (ICI) cancer therapy associated with significant mortality. To ensure patients continue to safely benefit from life-saving cancer therapy, an understanding of fundamental immunological phenomena underlying ICI myocarditis is essential. We recently developed the NOD-cMHCI/II-/-.

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The terminal oxidases of bacterial aerobic respiratory chains are redox-active electrogenic enzymes that catalyze the four-electron reduction of O to 2HO taking out electrons from quinol or cytochrome . Living bacteria often deal with carbon monoxide (CO) which can act as both a signaling molecule and a poison. Bacterial terminal oxidases contain hemes; therefore, they are potential targets for CO.

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Chinese lunar landing mission Chang'E-4 reached the far side of the Moon in January 2019 and has been providing unprecedented Lunar Penetrating Radar data able to explore the lunar subsurface down to more than 40 m (with its more resolutive high frequency band). Data are periodically released to the scientific community in raw PDS4 format. Here we provide different versions of the radar dataset after editing (i.

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One of the main functions of enzyme complexes that constitute electron transport (respiratory) chains of organisms is to maintain cellular redox homeostasis by oxidizing reducing equivalents, NADH and quinol. Cytochrome bd is a unique terminal oxidase of the chains of many bacteria including pathogenic species. This redox enzyme couples the oxidation of ubiquinol or menaquinol by molecular oxygen to the generation of proton motive force, a universal energy currency.

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In an effort to improve HLA-"humanized" mouse models for type 1 diabetes (T1D) therapy development, we previously generated directly in the NOD strain CRISPR/Cas9-mediated deletions of various combinations of murine MHC genes. These new models improved upon previously available platforms by retaining β2-microglobulin functionality in FcRn and nonclassical MHC class I formation. As proof of concept, we generated H2-Db/H2-Kd double knockout NOD mice expressing human HLA-A*0201 or HLA-B*3906 class I variants that both supported autoreactive diabetogenic CD8+ T cell responses.

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