Articles tagged with Organelles
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.
A new study found that inducing mitochondrial reactive oxygen species (ROS) during embryonic development protects the adult heart from chemotherapy toxicity in mice. The study discovered that stressed mitochondria release citrate, leading to long-term epigenetic changes that promote beneficial mitohormetic adaptations. These findings s...
Researchers found that energy-demanding tissues have larger macrophage crews to manage waste, with the number of macrophages tracking mitochondrial activity and waste production. This system is critical for tissue health and function, and may help preserve tissue function as we age.
A $2.1 million NIH grant will support research into the primary cilium's functions in protein synthesis and energy production, with implications for neurological disease. The study will investigate the role of primary cilia in embryonic brain development and connect fundamental cell biology with neurological disorders.
A team of researchers from the University of Copenhagen has discovered a crucial communication system on cell surfaces that plays a significant role in heart development. Alterations in three key proteins can disrupt this system, leading to congenital heart defects.
Researchers discovered a structural aberration in octopus ribosomes that enhances accuracy and reduces errors in protein synthesis. This finding may be linked to the evolution of the octopus's complex sensory system, which includes a highly sensitive 'taste by touch' system.
By coating extracellular vesicles with metal ions, cells can recognize and capture their own vesicles more strongly, improving liquid biopsies and aiding in drug delivery, rejuvenation, and more. This technique amplifies signals indicating cancer cells by a factor of 10,000, making single cells detectable even in large samples.
The OU College of Medicine has received a $10.7 million NIH grant to study how cells sense their environment and respond to diseases that occur when this process malfunctions.
Scientists have successfully created programmable supramolecular polymers in neutral lipid environments, such as triolein-rich lipid droplets. This breakthrough provides a new method for regulating cellular functions and has potential applications in treating diseases involving lipid droplets.
This study defines IFRD1's disease-protective function and elucidates its molecular regulatory mechanism, which suppresses de novo hepatic lipogenesis by boosting α-KG production. Clinical correlations and translational potential are also established for therapeutic interventions targeting the GLUD1/α-KG axis.
Researchers discovered a structural adaptation supporting the survival and mobility of a Dead Sea single-celled organism in harsh environments. The archaeal filament, powered by a membrane-anchored protein motor, is stiffened and strengthened with a unique outer sheath structure to facilitate movement in viscous conditions.
Researchers have developed a new method to build programmable artificial organelles inside living cells using RNA, enabling customization of cellular compartments and tunable properties. This approach may lead to specialized biological functions for nanomedicine and gene engineering.
Researchers developed a nasal spray that reversibly reduces brain inflammation, restores cellular power plants, and improves memory. The treatment bypasses the brain's protective shield through intranasal delivery, suppressing chronic inflammation and promoting successful brain aging.
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.
A Waseda University research team developed a nanotube membrane-based injector to directly and reliably manipulate the cytoplasmic composition of living cells. The system successfully transferred cytoplasmic contents, including mitochondria, into target cells with high efficiency and minimal damage.
Researchers identify 'mitochondrial pearling' as key process for maintaining uniform spacing of nucleoids in mitochondria. Pearling involves a transient transformation that helps redistribute mtDNA clusters, ensuring efficient energy production and preventing disease.
Professor Timo Betz's project aims to develop synthetic materials that mimic key behaviors of living cells, including self-organization and physical adaptation. By studying the mechanical properties of living cells, he will recreate part of the cell's interior in a synthetic way.
Research by Amita Sehgal and her team reveals that sleep helps neurons stay healthy by removing oxidative damage through lipid transfer to glia cells. This process is crucial for maintaining neuronal function and may contribute to the development of neurodegenerative diseases like Alzheimer's.
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.
Bacteria move through liquids using propellerlike tails called flagella, which alternate between clockwise and counterclockwise rotation. Researchers propose a tug-of-war mechanism instead of the traditional equilibrium 'domino effect' model, where proteins lining the tail exert pressure on their neighbors.
Researchers develop experimental drugs that encourage mitochondria in cells to work harder and burn more calories. The findings offer a framework for designing safe and effective weight-loss treatments with potential benefits for metabolic health and neurodegenerative diseases.
Researchers used long-read sequencing to analyze the nuclear genome of Amorphochlora amoebiformis, revealing an extremely high proportion of introns (74%) compared to other eukaryotic genomes. The study provides important insights into the evolutionary dynamics and potential functional roles of introns in eukaryotic genomes.
Researchers in Japan discovered that cells eliminate less efficient ribosomes through a 'survival of the fittest' mechanism, ensuring accurate and efficient protein synthesis. This discovery sheds light on how cells maintain quality control and prevents ribosome-related diseases.
Research shows that high glucose levels cause mitochondria to move towards the periphery of pancreatic beta cells. This movement is linked to insulin secretion and may play a role in regulating blood sugar levels. The study found that inhibiting microtubules disrupted this process, suggesting a key role for these structures in mitochon...
Researchers have captured the most detailed images yet of molecules inside synthetic chromatin condensates, allowing them to understand how these droplet-like structures form and function. The team found that linker DNA length affects structure arrangement, which in turn dictates interactions between chromatin fibers.
Researchers discover GFAP's crucial role in regulating mitochondrial fusion and fission, a dynamic process that meets cells' energy needs. The study sheds light on Alexander disease, a genetic disorder caused by GFAP mutations, providing potential new avenues for therapies.
High-resolution label-free imaging reveals stable organelle dynamics and spatial organization, overcoming phototoxicity and halo artifacts. ExAPC microscopy captures biomolecular condensate-like structures and cellular responses to drugs.
Researchers at UTA discovered that mitochondria can protect a cell from dying by taking in calcium, regulating complex cell death. The findings offer insights into brain development and disease, potentially leading to targeted treatments.
Marine plankton rely on cilia for movement, feeding, and dispersal. A new study discovered that coordination of these tiny structures is maintained by short-range interactions between cilia, enabling the organism to swim even when damaged.
The development of a new pH probe, SITE-pHorin, offers precise organellar pH imaging in living cells. By harnessing quantum-entanglement interactions, the probe boasts unparalleled sensitivity and resolves long-standing controversies over mitochondrial and lysosomal pH.
The 2-day conference focuses on bridging the fields of mitochondrial biology, microbiome research, and extracellular vesicle science to advance translational innovation. Experts will discuss EVs as core messengers in intercellular communication and their potential therapeutic applications.
Researchers from The University of Osaka discovered that macrophages can directly engulf and digest damaged mitochondria through a process called microautophagy. This process allows lysosome-like compartments in macrophages to take in broken cell components directly, bypassing the need for digestion.
Cryo-optical microscopy captures high-resolution, quantitatively accurate snapshots of dynamic cellular processes at precisely selected timepoints. This technique enables the observation of transient biological events with unprecedented temporal accuracy.
Newly developed DNA nanostructures form flexible, fluid, and stimuli-responsive condensates without chemical cross-linking. These findings pave the way for adaptive soft materials with potential applications in drug delivery, artificial organelles, and bioengineering platforms.
Researchers discovered that mitochondrial dysfunction triggers a sophisticated metabolic response in brown fat cells, rewiring key enzymes to produce D-2HG. This metabolite modifies the cell nucleus, changing gene expression and nuclear structure, promoting adaptation and altering cellular identity.
Researchers at Nagoya University have developed a new lipid nanoparticle that delivers mRNA five times more efficiently, allowing better delivery of genetic instructions to cells. The study showed significant improvements in mRNA delivery and effective suppression of tumor growth in mice.
An international team has uncovered a new mechanism by which mitochondria and peroxisomes work together to defend against oxidative stress, maintaining cellular health. This discovery challenges the long-standing idea that cellular defense is confined within individual compartments.
Researchers have made a breakthrough in understanding malaria parasite proteins that could lead to targeted therapies. Two key proteins, PfRAP03 and PfRAP08, regulate gene expression in the apicoplast, a unique organelle found in P. falciparum. The loss of either protein led to parasite death, confirming their essential roles.
Two key proteins, Oxr1 and Ncoa7, regulate V-ATPase to maintain optimal luminal pH for glycosylation within the Golgi apparatus and trans-Golgi network. This discovery provides new insight into congenital disorders of glycosylation and their cellular mechanisms.
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.
Researchers have successfully modeled the synaptic vesicle cycle with unprecedented detail, shedding new light on how our brains function. The model predicts parameters of synaptic function that could not be tested experimentally, opening new avenues for neuroscience investigations.
Researchers have uncovered the mechanism by which ATP enters the endoplasmic reticulum, a process crucial for cellular function. The study reveals SLC35B1 as the key transporter protein, providing a promising target for therapeutic intervention.
Researchers at the University of Basel discovered that mitochondrial proteins assemble into large supercomplexes, crucial for providing cells with energy. These findings may lead to insights into human diseases and biotechnology applications.
A team of biologists has found that the endosymbionts of Strigomonadinae have lost virtually all genes required for division, instead relying on a nucleus-encoded protein to control their movement. This discovery provides insights into the evolution of organelles from bacteria and could lead to the development of synthetic symbiosis.
Researchers used super high-resolution 3D electron microscopy images to study primary cilia in mouse brain tissue, revealing new information about their organization and function. The findings provide insights into how cilia behave in their natural environment and could help scientists understand their role in disease.
Researchers have developed a method that precisely defines the locations of proteins within cells, revealing their relationships with one another. The team created a high-resolution map that organizes proteins according to their compartmentalization, providing crucial insights into cellular organization and response to infections.
Researchers have reviewed the therapeutic potential of extracellular vesicles derived from mesenchymal stem cells in treating inflammatory bowel disease. The study highlights the immunomodulatory, pro-regenerative, and anti-apoptotic properties of these vesicles, which may offer a safer alternative to conventional therapies.
Scientists have found that biomolecular condensates can cross membranes without specialized cutting proteins, a process called wetting, which is essential for plant survival. The study shows that these liquid droplets can exert large capillary forces on membranes, cutting them in two and enabling material exchange between cell parts.
Holotomography offers a promising approach to biomedical research, providing high-resolution images of live cells and tissues at the organelle level. The KAIST research team has developed core technologies and demonstrated its applications in various fields, including regenerative medicine and cancer research.
Researchers discovered that nuclei pack strongly, ordering cells into crystalline arrays, and control tissue stiffness. The study challenges the status quo, revealing a new role for nuclei in organ formation.
Kobe University researchers have discovered that the shimmering effect in some brown algae is due to the presence of tiny, uniform-sized spheres within cells called iridescent bodies. These microspheres reflect green light more than other colors, resulting in the alga's characteristic shine.
Researchers found that nutrient-starved cells divert ER exit sites to lysosomes for degradation, using a novel pathway to free up amino acids. This process involves the recruitment of molecules to direct ER exit sites to lysosomes, where they are destroyed and their components recycled.
Researchers found a symbiotic relationship between cyanobacteria UCYN-A and marine algae, B. bigelowii, where UCYN-A fix nitrogen gas into ammonium without regulating dinitrogen use. This suggests they may be on the path to becoming organelle-like structures.
Cells use autophagy as a recycling system to transport and break down damaged organelles, including mitochondria. A recent study reveals the molecular details of how an enzyme called TBK1 participates in mitophagy, a disease-relevant process linked to Parkinson's disease.
The Kobe University discovery identifies a new key player for synaptic function, revealing that the poorly characterized protein FAM81A interacts with at least three major postsynaptic proteins and modulates their condensation. The absence of this protein leads to a significant decrease in activity in cultured neurons.
A study published in PNAS reveals that HKDC1 protein plays a crucial role in maintaining mitochondrial and lysosomal function, thereby preventing cellular senescence. The researchers found that HKDC1 helps regulate the removal of damaged mitochondria through mitophagy and facilitates lysosomal repair.
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.
Researchers developed a convolutional neural network to identify structures in cryo-X-Ray-microscopy data, achieving high accuracy within minutes. The AI-based analysis method enables faster evaluation of 3D X-ray data sets and has potential applications in studying cell responses to environmental influences.
Researchers discovered a novel technique to identify p62-body constituents, revealing a major subunit of the supramolecular protein complex vault. Vault-phagy, the degradation of vault through selective autophagy, regulates homeostatic vault levels and may be associated with liver cancer.
Scientists create a subcellular omics toolkit to study organelle diversity and communication in stem cells. The tool enables the identification of similar cell types, leading to more precise therapies for various diseases.