Syncell is pleased to announce our attendance at the FASEB Molecular Metabolism: Cells and Systems conference. We will be showcasing our research poster titled "Identifying novel peri-droplet-mitochondrial interface proteins of oleic acid-treated HepG2 cells using microscopy-guided subcellular spatial protein purification." This presentation highlights our innovative approach and the capabilities of Microscoop technology in identifying previously unrecognized protein constituents at the mitochondria-LD interface, paving the way for further functional examination associated with lipid regulation and Non-alcoholic fatty liver disease pathogenesis. Connect with our scientist Yen Ming Lin. The conference covers a wide range of important topics, such as emerging methods for analyzing the compartmentalization of metabolism at the cell and tissue levels, the latest advances in regulating metabolic physiology and organ crosstalk, outstanding questions and current areas of research in targeting GLP1, and how metabolites can function as signaling molecules. We look forward to participating in insightful discussions and networking with fellow researchers at the FASEB Molecular Metabolism: Cells and Systems Conference. #Syncell #MolecularMetabolism #FASEB2024 #MMCSRC
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Mitochondria as secretory organelles and therapeutic cargos In their enlightening publication, the authors unveil the groundbreaking roles of #Mitochondria beyond their conventional duty of energy generation within cells. 🌟 The research brings to light the phenomenon of mitochondria being secreted into the extracellular space, both under normal and pathological conditions, revealing their multifaceted roles in regulating metabolism, immune responses, and cellular differentiation/maturation. 🌱 This intriguing discovery of mitochondria's extracellular activities opens up new vistas in understanding how these organelles influence various biological processes. Moreover, the authors discuss the promising therapeutic potential of mitochondria, evidenced by the positive outcomes from local or systemic mitochondrial administration in diverse disease models. 🚀 Highlighting the ongoing clinical trials and successful animal model studies, the publication underscores mitochondria's potential as innovative therapeutic agents. This research not only expands our comprehension of mitochondrial functions but also paves the way for novel treatment strategies leveraging the untapped potential of mitochondria. 🎯 #Bioinnovation #TherapeuticIntervention #ClinicalTrials #CellularBiology #RegenerativeMedicine #InnovativeResearch link: https://lnkd.in/gNjFAAAp
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𝗖𝗮𝗻 𝗻𝗮𝗻𝗼𝗯𝗼𝗱𝗶𝗲𝘀 𝗻𝗲𝘂𝘁𝗿𝗮𝗹𝗶𝘇𝗲 𝘀𝗻𝗮𝗸𝗲𝗯𝗶𝘁𝗲 𝘃𝗲𝗻𝗼𝗺? Learn more and read the paper here: https://lnkd.in/dWc8FpsW In this 7th paper together, DTU - Technical University of Denmark and Sophion Bioscience have published on nanobodies (the part of an antibody that binds to specific peptides) that can bind and neutralize the key active components found in coral snake venom. Dr. Melisa Benard Valle, PhD & colleagues in professor Andreas Laustsen-Kiel’s lab used a variety of antibody/nanobody discovery techniques to find an oligoclonal mix to bind and neutralize a variety of venom peptide components. Via the Qube 384 nAChR channel recordings, Sophion’s Dr. Kim Boddum showed the venom alpha-neurotoxin neutralizing capacity of these nanobodies. Finally, professor Alejandro Alagon’s lab at Instituto de Biotecnología UNAM showed these nanobodies increased mouse survival rates in envenomation studies. Congratulations to all authors on this Nature Communications paper that takes us another step closer to finding treatments for snakebite, a World Health Organization designated neglected tropical disease. #Toxins #Venom #PhageDisplay #AntiBody #Qube384 #AutomatedPatchClamp #IonChannels #DrugDiscovery #Electrophysiology #Sophion
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#citation Exciting research breakthrough in #liverhealth ! 🌟The recent research from Southern Medical University delves into the intricate mechanisms of iron metabolism in Nonalcoholic Fatty Liver Disease (NAFLD) and reveals the crucial role of Caveolin-1 (Cav-1). Researchers used specialized mouse models and in vitro experiments to unravel the impact of Cav-1 on liver health. Key takeaways: ✅ NAFLD disrupts lipid and iron metabolism. ✅ Reduced Cav-1 levels worsen iron metabolism in NAFLD. ✅ Cav-1 protects against oxidative stress. ✅ Macrophages with Cav-1 impact iron accumulation. ✅ Cav-1 predicts iron-related changes in NAFLD patients. These groundbreaking insights emphasize the significance of Cav-1 as a target protein in regulating iron and lipid metabolism. It holds promise for predicting and safeguarding against NAFLD development. Read more here: https://lnkd.in/gmpJZHRC Cyagen is proud to be part of this research with our Cav-1ᶠˡᵒˣ/ᶠˡᵒˣ mice. Check out our services here: https://lnkd.in/gjext7gN #knockout #liverdisease #mice #sciencecommunication #research #researchinnovation #researchpaper #biotechnologie #biotech #biotechnology
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Enhance Your Cystic Fibrosis Research with Our Synthetic Cystic Fibrosis Models (SCFM) Are you ready to take your CF research to the next level? At SynthBiome, we are proud to offer high-quality Synthetic CF Media designed to meet the rigorous demands of modern CF research. Why choose our SCFM Model? · Realistic Conditions – SCFM is meticulously formulated to replicate CF sputum, providing a reliable model for studying pathogens such as P. aeruginosa and S. aureus. · Consistent and Reproducible – standardized composition ensures consistent results, making your research reliable and comparable across different studies and laboratories. · Enhanced research outcomes – With our SCFM, you can identify therapeutic targets and research new treatment avenues in an in vitro environment that closely mimics the actual conditions of CF patients. · Save Time and Resources – Spend less time adjusting variables and more time on experiments. What sets us apart? · Most Accurate Model for Human CF Lung · Quality Assurance · Customer Support · Sole Producer – we are currently the only commercial producer of Synthetic CF Models. Ready to improve your research? Contact us today to learn more about SCFM and how it can benefit your research. Let’s drive innovation together and make a significant impact on CF research. Visit Our Website: https://lnkd.in/eHv-CiKf Email Us: contact@synthbiome.com #CysticFibrosis #SCFM #BiomedicalResearch #Innovation #Healthcare #Microbiology #CFResearch #SynthBiome
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A great step towards realistic cell culture models
Enhance Your Cystic Fibrosis Research with Our Synthetic Cystic Fibrosis Models (SCFM) Are you ready to take your CF research to the next level? At SynthBiome, we are proud to offer high-quality Synthetic CF Media designed to meet the rigorous demands of modern CF research. Why choose our SCFM Model? · Realistic Conditions – SCFM is meticulously formulated to replicate CF sputum, providing a reliable model for studying pathogens such as P. aeruginosa and S. aureus. · Consistent and Reproducible – standardized composition ensures consistent results, making your research reliable and comparable across different studies and laboratories. · Enhanced research outcomes – With our SCFM, you can identify therapeutic targets and research new treatment avenues in an in vitro environment that closely mimics the actual conditions of CF patients. · Save Time and Resources – Spend less time adjusting variables and more time on experiments. What sets us apart? · Most Accurate Model for Human CF Lung · Quality Assurance · Customer Support · Sole Producer – we are currently the only commercial producer of Synthetic CF Models. Ready to improve your research? Contact us today to learn more about SCFM and how it can benefit your research. Let’s drive innovation together and make a significant impact on CF research. Visit Our Website: https://lnkd.in/eHv-CiKf Email Us: contact@synthbiome.com #CysticFibrosis #SCFM #BiomedicalResearch #Innovation #Healthcare #Microbiology #CFResearch #SynthBiome
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Zheng D, Soh BS, Yin L, Hu G, Chen Q, Choi H, Han J, Chow VT, Chen J. Differentiation of Club Cells to Alveolar Epithelial Cells In Vitro. Scientific Reports, 2017, Jan 27;7:41661. doi: 10.1038/srep41661. This study details a protocol for inducing the differentiation of club cells into alveolar epithelial cells in a controlled in vitro environment, identifying specific molecular and cellular cues that guide this differentiation process. This knowledge is essential for comprehending lung development and repair mechanisms. This approach not only provides a model system for studying lung cell differentiation but also contributes to the understanding of cellular plasticity within the respiratory epithelium. The findings from this study offer a valuable contribution to the field of respiratory biology, unraveling the mechanisms involved in the differentiation of club cells to alveolar epithelial cells. The research has implications for understanding lung development and regeneration, with potential applications in respiratory disease modeling and therapeutic development. The publication represents a significant step toward deciphering the complexities of cellular differentiation in the lung epithelium. Read the article here: https://lnkd.in/d7SVWU7R #stemcells #Haematopoiesis
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check out these opportunities
We are looking for motivated Ph.D. and M.Sc. students to join our molecular physiology lab! Find out more about our research interests at https://lnkd.in/evf9vJD4
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Professor and Scientific Director, Center for Alimentary and Metabolic Science at University of California, Davis
Myoglobin is an abundant protein in muscle and heart, long-believed to play a key role in oxygen delivery to support oxidative metabolism. More recent findings question this dogma and suggest there's much more to the story: myoglobin's role likely involves regulation of cell metabolism signaling cascades and lipid trafficking. These perspectives can be found in our newly-published open access paper in the preeminent physiology journal Physiological Reviews, co-written with Drs. Chintapalli, Adepu, and Anishkin. https://lnkd.in/g4PD5rDE We hope this paper will be an important resource for exercise scientists, bioenergetics fanatics, and brown fat researchers.
A versatile delivery vehicle for cellular oxygen and fuels, or metabolic sensor? - A review and perspective on the functions of myoglobin | Physiological Reviews
journals.physiology.org
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AZAFAROS B.V. is thrilled to make two important announcements: 📜8 posters selected for presentation at upcoming international conference on lysosomal storage disorders, the WORLDSymposium™. 📊 Results of the first-in-human Phase 1 study testing the safety in healthy volunteers of our lead asset, nizubaglustat, have been published in leading peer-reviewed journal, Molecular Genetics and Metabolism. Four posters showing baseline data from our landmark natural history (PRONTO) study in patients with GM1 and GM2 gangliosidoses were among the eight selected for presentation at the WORLDSymposium™, to be held at the Manchester Grand Hyatt Hotel in San Diego from 📅 February 4-9. Other posters include the design of our Phase 2 RAINBOW study investigating nizubaglustat in patients with GM2 gangliosidosis and Niemann-Pick disease type C (NPC). Additionally, we will present results from a novel human 🧠 brain organoid model of GM1 gangliosidosis in collaboration with the Australian Institute for Bioengineering and Nanotechnology AIBN. Azafaros is proud to present these clinical trial achievements 🎯 as we work closely with investigators, patient advocacy groups and investors towards finding treatment solutions for families and patients with GM1, GM2 and NPC. 📰 You can read the full story here: https://lnkd.in/e8k8pmc5 #Biotech, #clinicaltrials, #investors, #GM1, #GM2, #NPC, #organoid, #worldsymposium, #Teamwork, #RareDiseases, #Azafaros
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LHI Lecture Feb. 28, noon: “Trem2 Regulates Foamy Macrophage Function in Atherosclerosis” Michael T. Patterson, B.S. MSTP (MD/PhD) Student Jesse Williams, Ph.D. Lab Department of Integrative Biology and Physiology University of Minnesota Medical School More about Dr. Patterson from the Williams lab website: https://lnkd.in/dKpGgKP9 Location: 1-101 Microbiology Research Facility (MRF) 689 23rd Ave SE, Minneapolis, MN Map: https://lnkd.in/gu3dWwms Webcast @ z.umn.edu/lhi-webcast Learning Objectives 1. Trem2 regulates foamy macrophage cholesterol uptake% survival and proliferation within atherosclerotic lesions. 2. Trem2 signaling drives liver-X-receptor mediated cholesterol efflux and metabolic homeostasis to inhibit ER stress and promote foamy macrophage survival under lipid loaded conditions. 3. Trem2 agonism promotes foamy macrophage survival and pro-resolving functions to drive atherosclerotic plaque stability.
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