Articles tagged with Cell Metabolism
A study by IRCCS Fondazione Istituto Neurologico Carlo Besta and Politecnico di Milano demonstrates that innovative materials can coat mitochondria without compromising their function. The coating method retains the mitochondria's ability to produce energy.
Researchers at Sanford Burnham Prebys discovered that blocking an energy transfer enzyme shifts mammalian hearts into a regenerative state, promoting regeneration and improving recovery after a heart attack. By modulating heart cell metabolism, scientists can potentially awaken the heart's dormant regenerative abilities.
Salk Institute researchers have discovered a novel pathway that links chronic interferon II exposure to mitochondrial dysfunction, leading to immunosuppression and enhanced tumor growth. By blocking prostaglandin E2, they found a viable target to restore immune system function and combat immunotherapy resistance.
Researchers have identified GW406108X, a broad-spectrum antiviral compound, that can inhibit a range of enteroviruses, including EV-D68, by targeting a process in human cells. The compound showed activity against multiple viruses, including Rhinovirus A16, and reduced EV-D68 levels by 1,000-fold in laboratory experiments.
Researchers have discovered the underlying mechanism of Atg2-mediated lipid transfer in autophagy, revealing two distinct mechanisms that enable proper growth of the autophagosomal membrane. The phosphorylation of a specific region of Atg2, mediated by Atg1, enables its binding to the endoplasmic reticulum and subsequent lipid transfer.
Researchers have developed a nondestructive imaging technique to measure single-cell immune metabolism in real patient blood samples, providing a higher level of information than current clinical techniques. This breakthrough could improve disease diagnosis and treatment for conditions like blood cancers, lupus, and sepsis.
Researchers uncover ancient energy-sensing signaling cascade in marine oysters that sheds light on human lung adenocarcinoma. The KAT2/HDACIIa–PGK–ALDO axis promotes glycolytic flux to ensure cell survival under energy stress.
Researchers at Brown and U.T. Southwestern have identified a key mechanism underlying GPT2 deficiency, a rare genetic disease affecting brain development. Supplementing a metabolite called alpha-ketoglutarate may improve DNA structure and gene expression in the brain, potentially leading to new treatments.
Researchers at Gladstone Institutes found that hypoxia therapy can extend lifespan and improve brain function in mice with motor neuron degeneration. The therapy works by reducing the amount of oxygen available to cells, which can help counteract the effects of defective mitochondrial quality control machinery.
Research reveals birds can harness lactate to rapidly resurrect blood function, outperforming mammals. Lactate enables bird RBCs to convert methaemoglobin back to haemoglobin three times faster than mammalian RBCs.
Researchers identified two parallel neuronal circuits regulating autophagy-lysosome pathway in C. elegans body wall muscle. The first circuit involves electrical synapses and the second originates from ASI sensory neurons, both converging on a Ca2+-calpain-lysosome signaling cascade to maintain muscle homeostasis.
Researchers found that obesity alters the biological changes in breast cancer cells, enabling them to survive and thrive. The study's findings could improve prediction and treatment of invasive breast cancer, reducing overtreatment and unnecessary treatments.
Researchers at Trinity College Dublin found that cells with latent TB remain metabolically flexible, allowing strong antibacterial responses. In contrast, cells from people with active TB disease show impaired metabolism and weaker responses to infection.
Researchers identify TGF-β signaling pathway as key regulator of osteoblast quiescence, suggesting its inhibition can aid in reactivation of dormant osteoblasts. Combining TGF-β-blocking antibodies with anti-sclerostin treatment shows promising therapeutic potential for osteoporosis treatment.
A team of researchers has identified a key mechanism in the degeneration of motor neurons in ALS, revealing that chaperone-mediated autophagy is significantly reduced in patients. This finding suggests that this cellular system may be a potential therapeutic target to slow disease progression.
Salk Institute researchers have developed a new biological platform for studying mitochondrial DNA in human physiology, adaptation, and therapeutic development. The platform allows scientists to investigate mitochondrial DNA variation in health and disease, enabling therapeutic innovation for mitochondrial disorders.
New MSK research reveals that the TCA cycle's waste-management function may present an opportunity against cancer, microplastics impair immune 'housekeeping' functions and TOX plays different roles in different immune cells. A new combination approach for treating advanced kidney cancer after immunotherapy has also been identified.
For the first time, researchers have directly visualized how newly formed cellular organelles leave the endoplasmic reticulum and transition onto microtubule tracks inside living cells. The study reveals that the ER plays an active role in steering intracellular traffic.
A new study has created a comprehensive atlas of lysosomal proteins in the brain, shedding light on the functions and dysfunctions of these cellular components. The data, which includes 790 proteins associated with lysosomes, could help scientists better understand neurodegenerative diseases such as Alzheimer's and Parkinson's.
Researchers summarize itaconate biology highlighting its chemical reactivity and therapeutic potential in treating infectious diseases, sepsis, autoimmunity, neurodegenerative disorders. Itaconate exerts biological effects through post-translational modifications, altering protein activity and signaling pathways
A study conducted at the University of California, Riverside, has uncovered a link between soybean oil consumption and obesity in mice. The research found that a genetically engineered group of mice on a high-fat diet rich in soybean oil did not gain weight, suggesting that the liver protein HNF4α plays a crucial role in fat metabolism.
Researchers discovered that brain enzyme OTULIN regulates tau protein accumulation and has implications for treating neurodegenerative diseases. The study revealed OTULIN's role in controlling gene expression and RNA metabolism, suggesting a potential therapeutic target.
A new approach allows scientists to directly correlate gene expression with metabolite abundance, enabling the elucidation of complex plant natural product biosynthetic pathways. This method can help identify specialized cell types involved in producing therapeutically relevant chemical compounds.
Scientists discovered that the APOE4 gene blocks brain cells from using alternative energy sources as we age, significantly increasing Alzheimer's risk. This knowledge could pave the way for new treatments by targeting lipid metabolism.
Researchers discovered a ubiquitin precursor form, CxUb, that amplifies abnormal protein destruction under stress, supporting healthy regeneration. This unique mechanism may lead to improved therapies for cancer and neurodegenerative diseases.
Researchers exploring how exercise stress affects cellular adaptations and disease risk, focusing on mitochondrial energy sensing and AMPK activation. The study aims to determine if increasing mitoAMPK activity can mitigate diabetes in skeletal muscle.
Researchers tracked the movement of fluorescent particles inside the cells of microscopic worms, providing unprecedented insights into cellular crowding. The study found that the cytoplasm inside the worms was significantly more crowded and compartmentalized than in single-celled yeast or mammalian tissue culture cells.
A team of scientists has developed a protein-based therapeutic tool called Crunch to target and remove specific living cells, such as cancer cells or overactive immune cells. The new system uses the body's natural waste removal system to clear out unwanted cells, offering hope for improved treatments.
Researchers have identified a key gene crucial for vitamin D uptake and metabolism, offering new avenues for precision medicine in cancer therapy and potential benefits for autoimmune diseases. Inhibiting this gene may selectively kill cancer cells while leaving healthy tissues unharmed.
Scientists from UC San Diego develop an artificial cell membrane that can remodel itself through metabolic activity, shedding light on how life may have emerged on prebiotic Earth. This breakthrough could lead to advancements in drug delivery, biomanufacturing and environmental remediation.
A study by the Center for Redox Processes in Biomedicine presents a valuable new experimental model for investigating the interaction between the proteasome and mitochondrial function. The proteasome plays a role in protein quality control, while mitochondrial metabolism affects protein degradation efficiency.
Scientists found that blocking PTGIR could help revitalize T cells in their battle against cancer. Prostacyclin interacts with PTGIR to lead to T cell exhaustion, which can be reversed by inhibiting this interaction.
Researchers have discovered a novel cell-clearance pathway linked to diseases such as Chediak-Higashi Syndrome, which affects immune system function. The study used CRISPR/Cas9 gene-editing technology and live imaging to characterize this pathway and identify key genes involved.
Researchers developed a systems approach to measuring organelle changes in living cells as they grow. The study found that certain organelles grow faster than others and that the vacuole plays a key role in buffering the cell against randomness.
A high-fat diet leads to metabolic enzyme dysregulation, insulin resistance, and accumulation of reactive oxygen species in cells. Reversing these effects with antioxidants can mitigate damage.
A decade-long project has provided the first comprehensive functional blueprint of chemical transport pathways in human cells. The RESOLUTE consortium's groundbreaking studies have more than doubled existing knowledge on solute carriers, offering powerful new resources for biomedical discovery.
Estrogen-related receptors play a crucial role in regulating muscle cell metabolism and energy production. Researchers discovered that these receptors can increase mitochondrial numbers and enhance energetic output when muscles need more energy, making them a promising therapeutic target for metabolic disorders.
Scientists have discovered a mechanism that controls tomato ripening, regulated by autophagy, which also affects life- and health-span in humans and animals. This finding has significant implications for reducing food waste and addressing sustainable food security.
Researchers at Pennington Biomedical Research Center investigated tirzepatide's effects on weight loss and metabolic health. The study found that tirzepatide decreased calorie intake and increased fat oxidation, leading to significant weight loss. However, the drug did not decrease the slowing down of metabolic rate usually observed wi...
A team of researchers has identified a novel oncometabolite that accumulates in tumors and impairs immune cells' ability to fight cancer. The study highlights how the metabolic environment of tumors influences T cell function, opening new possibilities for improving cancer immunotherapy by targeting tumor metabolism.
Low-dose microplastic exposure leads to abnormal reproduction in females, characterized by oocyte meiotic maturation defect and H4K16 hyperacetylation. HDAC3 insufficiency is proposed as a key mechanism underlying this toxicity.
Scientists have pinpointed a weakness in lung cancer's defenses by uncovering an enzyme that boosts cancer cell metabolism to fuel growth. Researchers identified GUK1 as a metabolic enzyme that plays a crucial role in ALK-positive cancers, suggesting it may be a target for new therapies.
Scientists have developed genetically encoded biosensors to measure the ratio of NADPH to NADP⁺ in real-time, revealing new insights into cellular detoxification and protective function.
Researchers have discovered two previously unknown bacterial species in deep-sea corals from the Gulf of Mexico. These bacteria have extremely reduced genomes and lack the ability to break down carbohydrates, surviving on amino acids instead. The discovery provides insights into the unique adaptations of deep-sea organisms.
Scientists discovered a unique way in which yeast cells adapt to starvation by coating their mitochondria with massive molecular complexes called ribosomes. This adaptation has potential implications for cancer treatment as it may help overcome the challenges faced by cancer cells when they are starved of nutrients.
A team of researchers created RENAISSANCE, an AI-based tool that simplifies the creation of kinetic models to accurately depict metabolic states. The tool successfully generated models that matched experimentally observed metabolic behaviors in Escherichia coli, simulating how the bacteria would adjust their metabolism over time.
Researchers used optical metabolic imaging to study the effects of Toxoplasma gondii infection on host cells. They found that infected cells became more oxidized and had changes in glucose and lactate levels, highlighting the parasite's impact on metabolism.
Researchers at Goethe University Frankfurt have discovered thalidomide derivatives that target and degrade BCL-2, a protein essential for the survival of cancer cells. The derivatives bind to CRBN, reprogramming its binding surface to mark BCL-2 for degradation, ultimately leading to cell death.
A team of researchers at The Hospital for Sick Children discovered a way to potentially reduce toxic cellular waste in patients with Zellweger Spectrum Disorder. By increasing the autophagic limit, they observed improved clearance of cellular waste, offering new pathways for treatment.
Chicken sperm can retain fertility and viability for up to three weeks after refrigeration, making it unsuitable for traditional cryopreservation methods. The study found that removing calcium ions impacts energy metabolism dynamics, inducing a physiological dormancy-like state in the sperm cells.
A study published in EMBO Reports reveals that microautophagy is crucial for repairing damaged lysosomes, which helps prevent cellular aging. The researchers identified key regulators of this process, including STK38 and GABARAPs, and found that their depletion increases the rate of senescent cells and shortens lifespan in C. elegans.
A study published in The Journal of Physiology found that exercise suppresses hunger by acting on hormones and metabolites. Researchers suggest that understanding these mechanisms could lead to new treatments for obesity.
Scientists have discovered that tissue-resident memory T cells can be enhanced to fight off infections and tumors by redirecting their cholesterol-making process. A drug and statins were found to boost coenzyme Q production in these cells, improving their effectiveness.
Scientists have developed a new assay system to target lactate transporters SLC16A1 and SLC16A3, associated with certain cancers and diseases. The method enables the discovery of highly selective inhibitors, providing a potential new approach for cancer treatments.
A team of researchers from Goethe University Frankfurt has discovered a central switch point in the mitochondrial signaling chain under misfolding stress. The mitochondria send two chemical signals to the cell when protein misfolding stress occurs, triggering a protective response that reduces misfolded proteins and stabilizes membranes.
Researchers have successfully visualized the three-dimensional structure of human tRNA splicing endonuclease TSEN, a crucial enzyme in tRNA maturation. The study reveals how TSEN recognizes and excises introns from precursor tRNAs, shedding light on its role in neurodegenerative disorders like pontocerebellar hypoplasia.
A team of scientists led by Professor Ivan Đikić and Christian Hübner identified the role of ubiquitin in regulating ER-phagy, a process involved in the degradation of the endoplasmic reticulum. This discovery sheds light on neurodegenerative diseases caused by defective FAM134B and ARL6IP1 proteins.
Scientists at CNIO identify succinylation as a poorly studied mechanism in cancer research; mutated DLST protein prevents succinylation, leading to pseudohypoxia and tumor growth. Succinylation is crucial for protein function and may be linked to various diseases.
A study found that biological age in humans and mice increases rapidly in response to diverse forms of stress, only to reverse after recovery. The researchers used DNA methylation clocks to measure changes in biological age, revealing transient changes in response to stressful stimuli.
Researchers at Gladstone Institutes have made a groundbreaking discovery about how neurons consume and metabolize glucose, a process crucial for maintaining normal energy levels. The study found that neurons rely on glycolysis to break down glucose, and its disruption can lead to severe learning and memory problems in mice.