VITAL
The VITAL Research Symposium is an interdisciplinary event that showcases the latest cutting-edge research conducted by postdoctoral researchers across all disciplines within the Buck Institute for Research on Aging. The VITAL Research Symposium provides an excellent opportunity for scientists and community members to engage with the latest aging research, network with researchers, and participate in thought-provoking discussions.
The VITAL Research Symposium incorporates sessions for researchers, general audiences, and a panel highlighting alumni paths to successful careers.
We look forward to your participation and hope to see you healthy and VITAL at our next symposium!
Mark your calendars!
This year's VITAL symposium is Wednesday, September 18, 2024
Registration is now closed.
CENTER DETAILS
Agenda for VITAL symposium: September 18, 2024
9:00-9:30 |
Registration |
9:25-9:30 |
Introduction |
9:30-10:30 |
Keynote: Judith Frydman |
10:30-10:50 |
Bijoya Sen (Hansen Lab) – Understanding the nitty-gritty of the cellular clean-up crew: Differential interaction of Atg8 proteins with the autophagy receptor p62 in C. elegans |
10:50-11:10 |
Olga Bielska (Verdin Lab) – Uncovering a new gene linking aging and infertility |
11:10-11:30 |
Coffee Break #1 |
11:30-11:45 |
Presentation from Vector Builder |
11:45-12:45 |
Alumni Panel |
12:45-1:45 |
Lunch |
1:45-2:05 |
Heeun Jang (Garrison Lab) – Neural circuit mechanisms underlying dehydration risk in aged mice |
2:05-2:25 |
Olfat Malak (Haghighi Lab) – Role of Calcium Influx in Synaptic Homeostasis: Implication for Aging and Diseases |
2:25-2:45 |
Rais Kadir (Ellerby Lab) – The Longevity Gene APOE2 Enhances Pericyte Function and Resilience to Senescence Through Modulation of Lipid Metabolism |
2:45-3:05 |
Sudipta Bar (Kapahi Lab) – Breakdown of neuronal glycogen protects against tauopathy by shunting sugar to pentose phosphate pathway |
3:05-3:25 |
Coffee Break #2 |
3:25-3:45 |
Lay talk: Charlie Schurman (Schilling Lab) – The importance of skeletal aging |
3:45-4:05 |
Lay talk: Hiroshi Ebata (Hansen Lab) – Understanding Aging: The Importance of Taking out the Trash |
4:05-4:15 |
Concluding Remarks |
4:15-5:30 |
Poster Session/Reception |
Keynote Speaker
Judith Frydman, PhD
Donald Kennedy Chair in Humanities and Sciences and Professor, Departments of Biology and Genetics,
Stanford University
Biosketch
Judith Frydman grew up in Buenos Aires, Argentina, where she majored in Chemistry and received her PhD in Biochemistry from the University of Buenos Aires. She carried out her postdoctoral training with Ulrich Hartl at the Sloan Kettering Institute in New York, where she had two major contributions to the field of cellular protein folding. First, she discovered that eukaryotic cells have a ring-shaped chaperonin complex, which was termed TRiC and secondly, she established that, unlike what was previously believed based on biophysical experiments, protein folding in in eukaryotic cells occurs cotranslationally as polypeptides emerge from ribosomes during their biosynthesis. Importantly, she showed that distinct molecular chaperones are specifically recruited to bind ribosome-nascent chain complexes to assist cotranslational folding. These fundamental discoveries have shaped current thinking of protein folding in vivo. She is currently the Donald Kennedy Chair in Humanities and Sciences at Stanford University and a professor in the Departments of Biology and Genetics. She is an elected member of the National Academy of Sciences and of the American Academy of Arts and Sciences.
Research Interests
The central theme of Dr. Frydman’s research is to understand how cells maintain a healthy and functional proteome by focusing on biological mechanisms controlling cellular protein folding, aggregation and quality control. Her research has made important contributions to understanding protein homeostasis (proteostasis) in eukaryotic cells. Her lab discovered that distinctly regulated proteostasis networks mediate cotranslational folding and protection of the proteome from proteotoxic stress. She also established the key role of spatial sequestration of misfolded and aggregated proteins in specific membrane-less cellular compartments in proteome quality control and defined how chaperone-dependent pathways cooperate with specific components of the ubiquitin-proteasome system to mediate cytoplasmic and nuclear misfolded protein quality control. Her lab also harnesses these insights to develop therapeutic approaches to ameliorate human diseases including neurodegenerative and viral infectious diseases. Work in the Frydman lab has also identified specific interventions that disfavor the production of toxic protein species; efforts are now focused on the link between aging and loss of cellular robustness.
The alumni panel is organized by the Buck Biotech Group.
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Nick Aguirre Senior Scientist, Regel Therapeutics
For the human body to develop and function normally, the precise level of expression of each gene of the genome needs to be tightly regulated by epigenetics. When this balance is disrupted, alteration in gene expression can lead to severe genetic diseases for which no cure is available. Regel’s technology utilizes a deactivated Cas system (dCas) which targets the epigenome without editing or damaging the DNA. This approach harnesses the natural mechanisms of gene regulation, allowing for efficient and permanent restoration of normal gene expression. See more at: https://regeltherapeutics.com/
Major Accomplishments: Previously, I completed my PhD work in skeletal muscle physiology at UC Davis and postdoctoral work at The Buck and UCLA in mitochondrial transplantations. Exposure working with Unity Biotechnology during my tenure within Dr. Judith Campisi’s lab led me to pursuing a career within industry; wherein, I have worked with Juvena Therapeutics, Scribe Therapeutics, and Regel Therapeutics. At Juvena, I performed critical preclinical in vitro and in vivo work on JUV-161 contributing to the acquisition of CIRM and Series A funding. With Scribe, I established in vitro muscle testing platforms and developed assays for cardiometabolic diseases to screen gene therapy candidates across four different indications. Currently at Regel, I have been managing the IND-enabling in vivo work of our cardiac and skeletal muscle programs.
Future goal: My personal goal is to lead discovery and translational science teams from indication selection all the way through IND-enabling trials. Ultimately, I wish to see one or more of the drugs I help create make a positive impact on patients’ lives, enhancing their longevity, quality of life, independence, and happiness.
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Brenda Eap Vice President of Communications and Partnerships, The Alliance for Longevity Initiatives (A4LI)
A4LI is a 501(c)(4) non-profit organization dedicated to transforming aging through legislation and forward-thinking policies. Its mission is to extend healthy human lifespan by focusing on accelerating equitable access to next-generation therapies. More about A4LI here (https://a4li.org).
Major Accomplishments: Shortly after I defended my PhD work in the Newman lab in 2023, I transitioned into advocacy work with the Alliance for Longevity Initiatives (A4LI). One accomplishment I am proud of is planning A4LI’s first successful DC Fly-In to brief Members of Congress on geroscience. It was a 2-day event with our Longevity Science Caucus, longevity leaders, former politicians, and congressional staffers. I am excited to continue advocating for the future of 21st-century medicine through the hard work and advancements in the geroscience field!
Future goal: My goals are to continue influencing policymakers and MoC about geroscience research at our DC Fly-Ins, inspire everyone to get involved in getting their local representatives interested in the longevity biotech field, and lobby to strengthen communication between NIH and agencies like the FDA. By accelerating the availability of longevity therapeutics, we can improve the health and well-being of all Americans.
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Brian Hodge Senior Scientist, UCSF
Dr. Hodge earned his Ph.D. in 2015 from the University of Kentucky College of Medicine, where his research focused on the role of molecular clocks in peripheral tissues and their influence on homeostasis and function. Through the creation of a transgenic muscle-specific molecular clock mutant model, he identified accelerated aging phenotypes in skeletal muscle, sparking his deep interest in the aging field. He began his postdoctoral studies in 2016 in the laboratory of Dr. Pankaj Kapahi at the Buck Institute to investigate how lifespan-extending dietary interventions, such as dietary restriction influence circadian rhythms to delay aging and extend longevity in Drosophila. His research revealed that DR enhances the temporal transcriptional output of pathways that prevent age-related photoreceptor degeneration and identified the photoreceptor as a critical mediator of DR-induced lifespan extension. In 2021, he transitioned to industry, joining the venture-backed start-up Fountain Therapeutics as a Senior Scientist. There, he leveraged high-content imaging to screen for small molecule regulators of cellular aging. Early in 2024, Dr. Hodge joined the Small Molecule Drug Discovery center at UCSF. He currently works in collaboration with the Proteostasis Consortium on a multi-institute, Hevolution-funded project where he employs phenotypic imaging and deep learning to model age-related dysfunction within the proteostasis network and identify compounds that restore proteostasis in aging cells and neurodegenerative models.
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Ed Liao Director, Cell Biology, Kite Pharma
Kite pharma is a cell therapy company focused on treating and curing cancer. I currently lead the Molecular biology and Vector cores within research, developing the next generation of cell therapies. Our function supports the activities of project teams and process development.
I received my Ph.D. in Molecular Genetics from the University of Toronto, Canada. During my time at the Buck Institute, I studied the neuromuscular junction of Drosophila melanogaster in the lab of Dr. Pejmun Haghighi. My work in the field of neuroscience has been published in journals such as Nature and Neuron. I have 14 publications from my time in academia and 3 patents from my work in cell therapy.
My near term goals include developing the talent within my teams, and working to overcome the challenges of cell therapy. In my spare time I enjoy mountain biking, hiking and trail running.
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Chris Nelson CEO, Mpathy Bio Inc.
Major accomplishments:
1) I contributed genotyping algorithm development to a blood-typing test now adopted by the UK National Health Service (NHS). The test matches donor blood units with transfusion-dependent patients (often sickle cell and thalassemmia) who develop immunity against many blood surface markers. This more specific blood type matching gets patients blood their bodies will accept.
2) I helped build the bioinformatics and assay for a state-of-the-art cancer recurrence test called NeXT Personal. The liquid biopsy test is 100x more sensitive to low levels of circulating tumor DNA than other products on the market, and gives a 6-11 month lead time over detecting recurrence by imaging. This extra time helps patients and physicians adapt the course of treatment more effectively.
Future Directions: I have started a company developing multiomic organ damage biomarkers.
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Jordan B. Burton, PhD VITAL Research Symposium Chair
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Laurel Koch, PhD Keynote Speaker Selection Committee
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Kenny Wilson, PhD Postdoctoral Research Abstract Selection Committee
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Joanna Bons, PhD Life-Support Committee
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Kiyomi Kaneshiro, PhD Life-Support Committee
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Olfat Malak, PhD Life-Support Committee
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Parminder Singh, PhD Sponsorship Cultivation Committee
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Mitsu Nomura, PhD Alumni Panel Selection Committee
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Charlie Schurman, PhD VITAL Swag Committee
VITAL Research Symposium is pleased to acknowledge the generous support of the following major funders:
Thank you to our Sponsors!
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Thank you for your interest in supporting the postdoctoral researchers at the Buck Institute for Research on Aging!