Discovery Sciences Emerging Scholars Lectures
This lecture series features young scientists making notable discoveries as postdoctoral fellows or early career faculty.
Tuesday, November 1, Kelsie Eichel, Postdoctoral Fellow, Stanford University, 4:00 pm, 214 Light Hall: “How to Organize a Neuron: from C. elegans to Humans”
Dynamic protein organization within cells underlies fundamental biological processes. This is particularly evident in neurons, which are compartmentalized into distinct axonal and dendritic domains that require unique repertoires of proteins. Loss of polarity in neurons is associated with a wide array of pathologies, underscoring its importance. I identified a conserved and essential mechanism at the axon-dendrite boundary that changes our understanding of how neurons maintain protein compartmentalization over their long lifespan. I found that axonally and dendritically polarized receptors are cleared from the plasma membrane through endocytosis at the axon-dendrite boundary, which prevents receptor diffusion into the inappropriate compartment. Eichel CV Eichel Flyer
Thursday, September 29, Rita Brookheart, Assistant Professor, Washington University School of Medicine, 9:30 am, 206 Preston Research Building: “New Molecular Players Linking Muscle Metabolism and Growth”
Dr. Brookheart’s seminar focuses on her lab’s mechanistic work of how Site-1 Protease (S1P) controls mitochondrial metabolism in skeletal muscle. S1P is a Golgi-resident protease required for the proteolytic cleavage and activation of an array of transcription factors that are required to maintain and restore cellular homeostasis in response to ER stress and disruptions in cellular sterol/lipid levels. Dr. Brookheart’s lab previously identified a patient with a gain-of-function mutation in S1P who exhibited exercise intolerance and abnormal skeletal muscle mitochondrial morphology. Building on this study, her lab defined a previously unknown role for S1P in skeletal muscle metabolism and mass. Brookheart CV Brookheart Flyer
Thursday, April 21, Monica Santisteban, Instructor in Neuroscience, Brain and Mind Research Institute, Weill Cornell Medicine, 9:30 am, 206 Preston Research Building: “Cerebrovascular and Neuroimmune Mechanisms of Cognitive Impairment in Hypertension.” Co-sponsored by the Vanderbilt Brain Institute, the Department of Molecular Biology and Biophysics, the Department of Pharmacology, and the Vanderbilt Memory and Alzheimer’s Center.
Dementia affects almost 50 million adults worldwide,and is a major cause of death and disability. Vascular risk factors, such as hypertension and high-dietary salt, have gained importance since up to 50% of clinically diagnosed Alzheimer disease have a mixed pathology at autopsy including cerebrovascular lesions. Thus, elucidating novel mechanisms by which hypertension negatively impacts neurovascular and cognitive function is a necessary step to develop new approaches to protect the brain from hypertension. We have identified two distinct immune mechanisms, involving brain resident perivascular macrophages and circulating IL-17, contributing to cognitive impairment in mouse models of hypertension. Santisteban CV Santisteban Flyer
Mary Jane Tsang
Tuesday, April 12, Mary Jane Tsang, Postdoctoral Fellow at the Whitehead Institute for Biomedical Research, 4:00 pm, 1220 MRB III: “Setting a Timer for Mitosis: How Do Cells Slip Out?” Co-sponsored by the Department of Cell and Developmental Biology.
The Spindle Assembly Checkpoint is the key regulatory pathway that delays anaphase onset until mitotic chromosome segregation defects are corrected. However, in the presence of persistent, unresolvable errors, cells can undergo “mitotic slippage”, exiting mitosis into a tetraploid G1 state and escaping the cell death that results from a prolonged arrest. The molecular logic that allows cells to balance these dueling mitotic arrest and slippage behaviors remains unclear. We have uncovered that human cells modulate their mitotic arrest duration through the presence of conserved, alternative translational isoforms of the essential APC/C co-activator Cdc20, thus providing a new paradigm for controlling cell cycle events. Tsang CV Tsang Flyer
Thursday, March 10, Theresa Loveless, Associate Project Scientist, Department of Biomedical Engineering, University of California-Irvine, 12:00 pm, 202 Light Hall: “Ordered DNA Writing Enables Lineage Tracing and Analog Recording in Mammalian Cells.” Co-sponsored by the Department of Biochemistry.
Studying multicellular developmental processes can require the non-destructive observation of thousands to billions of cells deep within an animal. DNA recorders address this difficult task by converting transient cellular experiences into changes in the genome that can be sequenced later in high throughput. First, I will present a recently-published DNA recorder that acts primarily by writing new DNA, through the repeated insertion of random nucleotides at a single locus in temporal order, rather than by erasing as previous DNA recording technologies have done. Second, I will share the characterization of a new DNA recording architecture that maintains the strengths of CHYRON – ordered, information-dense recording – but (1) drastically reduces the rate of information loss through off-pathway mutations, (2) is in principle compatible with tens of rounds of recording, and (3) can in principle record at least tens of orthogonal inputs. Loveless CV Loveless Flyer
Alex J. Guseman
Thursday, December 2, Alex J. Guseman, Merck Fellow, University of Pittsburgh Medical School, 9:30 am, 202 Light Hall: “Peering into the Crystallin Ball of the Eye Lens.” Co-sponsored by the Department of Molecular Biology and Biophysics.
Cataracts, the opacification of the eye lens, are the leading cause of blindness worldwide. Cataracts form when the crystallin proteins of the eye lens are unable to maintain proteostasis and being to aggregate. As these aggregates grow, the lens opacifies, and visual impairment increases. Despite decades of research on the crystallin proteins, the mechanism of cataract formation is highly debated. Here we demonstrate in vitro that deamidation, a common post translational damage, has minimal impact to crystallin structure and biophysics, and highlight our progress to study crystallins in their native environment, the intact eye lens. Guseman CV Guseman Flyer
Tuesday, November 16, Daniel Gonzales, HHMI Hanna Gray Fellow, Purdue University, Weldon School of Biomedical Engineering, 2:00 pm, 1220 MRB III: “Micro- and Nano-scale Technologies for Mapping Sensory-Driven Activity from the Cortical Surface.” Co-sponsored by the Vanderbilt Brain Institute.
I will discuss a suite of flexible, transparent electrode technologies for high-density mapping of neural activity from the brain surface in behaving animals. Specifically, we show evidence that surface grids record biomarkers of subcellular activity that travel across the upper cortical layers during sensory stimulation. Thus, when we combine our grids arrays with existing technologies like silicon probes and two-photon imaging, we enable a platform for recording both subcellular dynamics and population-level outputs in awake animals. Gonzales CV Gonzales Flyer
Monday, November 8, Lauren Goins, Ph.D., Assistant Project Scientist, UCLA, 12:15 pm CT, 1220 MRB III: “New Paths and Pathways in Developmental Hematopoiesis.” Co-sponsored by the Department of Cell and Developmental Biology.
Fundamental questions remain unresolved in the hematopoiesis field such as how hematopoietic stem cells balance proliferation, differentiation, and specialization steps to produce the vast repertoire of blood cell types required for proper immune function. We have tackled this rather complex problem using a multi-pronged approach that combines transcriptomics, genetics, and mutational analysis using the Drosophila hematopoietic system as a model. In the hematopoietic progenitor state, we find that cell-extrinsic signals play a major role in controlling both spatial and temporal aspects of the cell cycle and their differentiation into mature cell types. In particular, we discovered that blood progenitors are maintained in a non-proliferative state in the G2 phase of the cell cycle by Wnt- and hedgehog-dependent signaling pathways that link cell cycle progression to differentiation. Furthermore, our analysis of crystal cells, platelet‐like cells involved in melanization, has uncovered new means by which Musashi and Numb affect canonical and non-canonical Notch signaling. We propose a model of how blood cells integrate various external inputs to determine cell cycle status and differentiation fate. Goins CV Goins Flyer
Maria Fernanda Forni
Thursday, October 14, Maria Fernanda Forni, Ph.D., Pew Postdoctoral Fellow, Yale University, 9:30 am CT, 208 Light Hall: “A Central Role for Metabolism in the Skin: Two Tales of How Adipocytes Can Impact Aging and Healing.” Co-sponsored by the Department of Molecular Physiology and Biophysics.
Metabolic regulation of tissue homeostasis is one of the most intriguing yet unexplored areas in skin biology. The skin consists of many different tissues and cell types that communicate in a regulated and timely manner to maintain organ homeostasis. As we age, this homeostasis is lost, and with it, the plethora of metabolic reactions that comprise normal homeostasis shift their balance, being perturbed or disrupted. Adipocytes are one of the key players in skin homeostasis regulation. They undergo drastic alterations during the processes of aging and wound healing. In this seminar, I will discuss how these cells are important for whole-body thermal homeostasis and metabolic fitness under conditions of limited energy intake. I will also address how these cells act as metabolic coordinators of immune cell function in the process of wound healing and how aging impacts these processes. Forni CV Forni Flyer
Friday, April 23, Sonya Neal, Ph.D., Assistant Professor, UC-San Diego, 12:00 pm CT: “Rhomboid Pseudoprotease Dfm1’s Role in ERADicating Multi-Spanning Membrane Substrates.”
Nearly one-third of membrane proteins are initially targeted to the endoplasmic reticulum (ER) membrane where they are correctly folded, assembled, and then delivered to their final cellular destinations. In order to prevent the accumulation of misfolded membrane proteins, ER associated degradation (ERAD) moves these clients from the ER membrane to the cytosol; a process known as retrotranslocation. Our recent work in S. cerevisiae has revealed a derlin rhomboid pseudoprotease, Dfm1, is involved in the retrotranslocation of ubiquitinated ERAD membrane substrates. Overall, our work seeks to advance the understanding of rhomboid pseudoproteases in membrane protein quality, a highly conserved process, which is implicated in a plethora of diseases such as cancer, Cystic Fibrosis and neurodegenerative diseases. Neal CV Neal Flyer
Friday, April 2, 12:00 pm CST via Zoom, Chrystal Starbird, Ph.D., Postdoctoral Fellow, Yale University, Department of Pharmacology: “Structural Basis of TAM Receptor Oligomerization.” Co-sponsored by the Department of Biochemistry.
Receptor tyrosine kinases are key regulators of a wide range of biological functions and share a single transmembrane helix that links an extracellular domain to an intracellular kinase domain. How a single helix promotes the large diversity of signaling mediated by RTKs has long been a question of interest. Classically, RTKs are considered to be activated by ligand-induced dimerization. However, my work on the TAM subfamily of receptors has shown unique requirements for oligomerization and suggests that our current simple view of receptor activation is insufficient to explain the observed complexity of receptor signaling. Starbird CV Starbird Flyer Get Zoom info here.
Tuesday, March 30, 4:00 pm CST via Zoom. Ana Arruda, Ph.D., Research Specialist, Harvard University School of Public Health, Cell and Developmental Biology. “Interorganelle communication in metabolic health and disease.” Co-sponsored by the Department of Cell and Developmental Biology.
Metabolically specialized cells display complex spatio-temporal organization of organelles in the tissue context to meet functional demands and adapt to challenges to maintain homeostasis. In this talk, I will discuss how different physiological and pathological nutritional states influence organelle morphology and interorganelle communication in liver and how alterations in these processes relates to the development of metabolic diseases. Arruda CV Arruda Flyer Get Zoom info here.
Wednesday, March 17, 9:00 am CST via Zoom, Daniel Castro, Ph.D., Acting Instructor, University of Washington, Department of Anesthesiology: “Next-Generation Approaches for Investigating Neuropeptidergic Circuits in Reward and Motivation.” Co-sponsored by the Department of Pharmacology.
Here I report that endogenous MOPR regulation of appetitive behavior in mice acts through a specific dorsal raphe to nucleus accumbens (NAc) projection. Select enkephalin-containing NAc ensembles are engaged prior to reward consumption, suggesting that local enkephalin release is the source of endogenous MOPR ligand. Selective modulation of NAc enkephalin neurons and CRISPR-Cas9-mediadated disruption of enkephalin substantiate this finding. Castro CV Castro Flyer Get Zoom info here.
Thursday, January 21, 4:00 pm CST via Zoom, Florentine Rutaganira, Ph.D., HHMI Hannah H. Gray Fellow, University of California-Berkeley: “Kinase Chemical Genetics in the Closest Living Relatives of Animals.”
Although all organisms use signal transduction to respond to external stimuli, the rise of multicellularity necessitated the evolution of signaling pathways to coordinate actions of individual cells into a singular response. As the closest living relatives of animals, choanoflagellates present a unique system to directly study the role of signaling pathways that were previously thought to be restricted to animals. High-throughput screening and activity-based kinase profiling within Salpingoeca rosetta, a choanoflagellate that differentiates into a rosette colony during its dynamic life history, provide evidence for a functional phosphotyrosine signaling repertoire that developed prior to the origin of animals. Rutaganira CV Rutaganira Flyer Get Zoom info here.
Friday, December 11, 12:00 pm via Zoom, Chelsey Spriggs, Ph.D., Postdoctoral Fellow, University of Michigan Medical Center: “Viral hijacking of host molecular motors to promote nuclear entry.” Co-sponsored by the Department of Biochemistry.
During entry, most DNA viruses must navigate the crowded cellular environment to reach the nucleus where transcription and replication of the viral genome occur. How polyomavirus (PyV), a small DNA tumor virus, accomplishes this feat is not well-understood. We reported that cytoplasmic dynein motor activity is required to disassemble PyV once in the cytosol and to target the disassembled virus to the nucleus. However, the precise mechanism underlying these dynein-dependent steps remain unclear. Investigating the role of dynein cargo adaptor proteins in this process, we have discovered an unexpected and novel function of the bicaudal-D adaptors in virus infection. Spriggs CV Spriggs Flyer Get Zoom info here.
Tuesday, December 8, 4:00 pm via Zoom, Christina Termini, Ph.D., University of California President’s Postdoctoral Fellow, UCLA: “Leveraging proteoglycans for hematopoietic stem cell regeneration.” Co-sponsored by the Department of Cell and Developmental Biology.
Although hematopoietic stem cells (HSCs) comprise less than 0.01% of the adult bone marrow, this rare cell population is capable of supporting the hematopoietic needs of an organism throughout their lifetime. However, when HSCs are unable to adapt to hematopoietic stress, life-threatening complications can arise. As such, it is essential we elucidate the basic regulatory mechanisms that underscore HSC regeneration. My postdoctoral research identified a novel surface marker that both identifies and regulates HSCs through parallel mechanisms. This surface marker is from the heparan sulfate family of proteoglycans and can be used to enrich for long-term HSCs capable of enhanced hematopoietic engraftment, expansion and self-renewal ability. Loss of function analyses determined that this heparan sulfate proteoglycan regulates HSC maintenance and myelopoiesis through alterations in cell cycling. Additional work analyzing how proteoglycans can be utilized to accelerate hematopoietic recovery after myelosuppression will be presented. Termini CV Termini Flyer Get Zoom info here.
Thursday, November 19, 9:30 am via Zoom, Cornelius Taabazuing, Ph.D., Postdoctoral Fellow, Memorial Sloan-Kettering Cancer Center: “Investigating the molecular regulation and function of death signaling complexes.” Co-sponsored by the Department of Molecular Physiology & Biophysics.
The cellular response to danger signals such as pathogens or DNA damage is important for survival and many diseases. The response is usually mediated by large multiprotein death signaling complexes that can either eliminate the damaged cells or promote homeostatic restoration pathways. However, the specific inputs that initiate the death signaling complex formation as well as the downstream signaling pathways activated by these complexes are not well understood. Here, we demonstrate how small molecule inhibitors of the serine peptidases, DPP8/9, induce formation of the CARD8 and NLRP1 inflammasomes, which activate caspase-1 to cause an immunostimulatory type of death called pyroptosis. Taabazuing CV Taabazuing Flyer Get Zoom info here.
Thursday, October 29, 9:30 am via Zoom, Melanie McReynolds, Ph.D., HHMI Hanna H. Gray Fellow, Princeton University, “NAD+ flux is maintained in aged mice.” Co-sponsored by the Department of Molecular Physiology & Biophysics.
NAD+ is an essential coenzyme found in all living cells. NAD+ concentrations decline during aging, but whether this reflects impaired production or accelerated consumption remains unclear. Here we employed isotope tracing and mass spectrometry to probe NAD+ metabolism across tissues in aged mice. In 25-month-old mice, we observe modest tissue NAD+ depletion without significant changes in circulating NAD+ precursors. Isotope tracing showed unimpaired synthesis of circulating nicotinamide from tryptophan, and maintained flux of circulating nicotinamide into tissue NAD+ pools. Although absolute NAD+ biosynthetic flux was maintained in most tissues of aged mice, fractional tissue NAD+ labeling from infused labeled nicotinamide was modestly accelerated. Long-term calorie restriction partially mitigated age-associated NAD+ decline despite decreasing NAD+ synthesis. Thus, age-related decline in NAD+ is driven by increased NAD+ consumer activity rather than impaired production. McReynolds CV McReynolds Flyer
Antentor “A.J.” Hinton, Jr.
Thursday, March 5, Antentor “A.J.” Hinton, Jr., Ph.D., 9:30 am, 206 Preston Research Building: “OPA-1 Deficiency in Skeletal Muscle Increases Mitochondria ER Contact Formation Through an ATF-4 Dependent Mechanism.”
Dr. Hinton, Jr. is a Postdoctoral Research Fellow in the Department of Internal Medicine, University of Iowa. In the laboratory of E. Dale Abel we have found that reduction in OPA1 (Optic Atrophy 1, a mitochondrial dynamin-like GTPase) expression in skeletal muscle results in endoplasmic reticulum (ER) stress response and FGF21 secretion. We predicted that there was an association between the loss of OPA1, an increase in ER-Mitochondrial Contact sites, and prevalence of diabetes. Mitochondrial endoplasmic reticulum contact sites (MERCs) are specialized membranes that are enriched with specific proteins believed to be important for calcium flux, lipid transfer, and mitochondria morphology. This observation provides a plausible mechanism linking altered mitochondrial dynamics with the activation of the ER stress response pathway and may give novel insight into how some patients develop insulin resistance. We propose to use this information to provide the foundation for future research that will lead to the discovery of more effective biomarkers that identify insulin resistance in skeletal muscle. Hinton CV Hinton Flyer
Tuesday, December 3, Chantell Evans, 4:00 pm, 206 Preston Research Building: “The Role of Optineurin in Neuronal Mitophagy.”
Dr. Evans is an HHMI Hannah H. Gray Postdoctoral Fellow at the University of Pennsylvania. Mitophagy, the selective removal of damaged mitochondria, is thought to be critical to maintain neuronal homeostasis. Mutations in proteins implicated in mitophagy, including PINK1, Parkin, OPTN, and TBK1, cause Parkinson’s disease or ALS, suggesting defective mitochondrial turnover contributes to neurodegeneration. To test this hypothesis, we used mild oxidative stress to induce low levels of mitochondrial damage in hippocampal neurons. We observed the sequential recruitment of Parkin, TBK1, and OPTN to depolarized mitochondria followed by their sequestration into autophagosomes, and determined this pathway was compartmentally restricted to the soma. Further, acidification of mitophagosomes was remarkably slow in neurons and overall was a rate-limiting step in the mitophagy pathway. Expression of an ALS-linked OPTN mutation disrupted the integrity of the mitochondrial network and this effect was exacerbated by oxidative stress. We propose that the slow kinetics of mitophagy enhance neuronal susceptibility to disease-associated mutations in the pathway, leading to neurodegeneration. Evans CV Evans Flyer
Reginald D. Cannady
Tuesday, November 12, Reginald D. Cannady, 4:00 pm, 512 Light Hall: “Probing Novel Targets to Reduce Heavy Drinking in Models of Alcohol Use Disorder.”
Dr. Cannady is a Postdoctoral Research Fellow at the Medical University of South Carolina. Individuals with alcohol use disorder (AUD) show an inability to regulate alcohol consumption and seeking behavior. Although, there are FDA‐approved medications for AUD, they have limited efficacy. My work examines neuroadaptations caused by chronic alcohol experience and focuses on identifying neuronal targets to reduce heavy drinking using several rodent models of alcohol addiction. This presentation will discuss the validation of KV3 potassium channels as a potential therapeutic target to reduce alcohol consumption in preclinical models of alcohol dependence. Cannady CV Cannady Flyer
Tuesday, October 22, Sabena Conley, 4:00 pm, 512 Light Hall: “Obesity-Induced Mesenchymal Stem Cell Senescence and Dysfunction.”
Dr. Conley is a Research Fellow at the Mayo Clinic College of Medicine, Rochester, Minnesota. Endogenous mesenchymal stem cells (MSC) mediate tissue repair, but obesity might potentially impair their regenerative potency. The adipose tissue microenvironment in obesity stimulates cellular senescence (CS), an irreversible cell cycle arrest that prompts an inflammatory, senescent-associated secretory phenotype (SASP). To test the hypothesis that obesity induces CS and dysfunction in MSC from obese patients, we harvested and evaluated MSC from fat tissue collected from obese and non-obese patients undergoing surgery at Mayo Clinic. Obese-MSC demonstrated increased CS and SASP and lower proliferation than non-obese-MSC. Therefore, human obesity induces senescence in adipose tissue-derived MSC, which might interfere with their repair capacity. Conley CV Conley Flyer
Thursday, April 25, Timothy Downing, 4:00 pm, 512 Light Hall: “Synthetic Genome Regulation for Cell and Tissue Engineering.“
Dr. Downing is an Assistant Professor in the Department of Biomedical Engineering, University of California, Irvine. The Downing Lab is interested in understanding how the chemical and biophysical microenvironment influences adult cell behavior and phenotype through epigenetic gene regulatory mechanisms. We hope to use this information in the design of next-generation biomaterials. This presentation will describe how specific cues (e.g., topography and matrix stiffness) within cellular microenvironments can influence epigenetic state and facilitate the reprogramming of somatic cells back to pluripotency. Web Downing Flyer
Tuesday, March 5, Luis Natividad, 4:00 pm, 206 Preston Research Building: “Impaired Endocannabinoid Signaling in Stress and Addiction“. Co-sponsored by the Vanderbilt Center for Addiction Research.
Dr. Natividad is a Senior Research Associate, The Scripps Research Institute, La Jolla. Abstract: “Heavy alcohol consumption induces long-term problems with stress and anxiety, and is common among dependent individuals who are co-diagnosed with mood disorders. As endocanna-binoids (e.g., N-arachidonoylethanolamine and 2-arachidonoylglycerol) provide an important mechanism of inhibitory constraint in the regulation of stress circuits, Dr. Natividad will elaborate more on the premise of dysregulated endocannabinoid signaling influenced by chronic alcohol exposure relative to observations in a genetic model of “innate alcohol dependence” within the central nucleus of the amygdala.” Natividad CV Web Natividad Flyer
Thursday, February 7, Stacey Finley, 4:00 pm, 512 Light Hall: “Systems Biology Approaches to Predict the Dynamics of Biochemical Networks in Cancer.”
Dr. Finley is an Assistant Professor at the University of Southern California. Abstract: “Systems biology approaches, including computational models, provide a framework to optimize effective therapeutic strategies for cancer. My research group develops mechanistic models of biochemical networks in cancer to study cancer immunotherapy, tumor angiogenesis, and cancer metabolism. Our models provide insight into the dynamics of the biochemical pathways in cancer and enable the development of novel therapeutics.” Finley CV Website Finley Flyer
Thursday, December 6, Angelina Hernandez-Carretero, 9:30 am, 206 Preston Research Building: “Novel Regulators of Obesity-Induced Insulin Resistance and Diabetes.”
Dr. Hernandez-Carretero is a Staff Scientist at the City of Hope Beckman Research Institute. “Further investigation is needed to understand the molecular players involved in obesity-induced insulin resistance. We have utilized a dietary switch mouse model to perform transcriptomics of the skeletal muscle, and compared these findings with RNA-seq of human obese- diabetic muscle. This multispecies approach identified key genes that tracked with the insulin resistant state in both mouse and human muscle, including Cysteine and glycine-rich protein 3 (Csrp3). Csrp3 expression is decreased in obese-insulin resistant muscle and plays an important role in insulin-stimulated glucose uptake.” Flyer Hernandez-Carretero CV
Tuesday, November 13, Luisa Escobar-Hoyos, 4:00 pm, 206 Preston Research Building: “Targeting RAS and mutant p53: Discovery of RNA splicing as a therapeutic vulnerability in pancreatic cancer.”
Dr. Escobar-Hoyos is a Postdoctoral Research Fellow at Memorial Sloan Kettering Cancer Center and Research Assistant Professor at Stony Brook University. “We recently discovered a novel mechanism of cooperation between the two most common oncogenes in pancreatic cancer, oncogenic RAS and neomorphic mutant p53, uncovering a potential therapeutic opportunity to target tumors that bear these mutations. Specifically, we found that mutant p53 causes aberrant splicing of GAP proteins, the negative regulators of RAS, resulting in expression of inactive GAP proteins (polyC GAPs), and ultimately promoting oncogenic RAS signaling. In addition, we identified that pancreatic tumors in mouse models depend on expression of polyC GAPs and splicing machinery proteins, as genetic and chemical inhibition of these proteins caused decrease in tumor growth, number of metastases and tripled the survival time of animals. These studies identified these proteins as new targets for tumors with neomorphic p53 and oncogenic KRAS. We expect to identify novel and specific dependencies of PDAC cells by studying and targeting specific alternatively spliced products and/or manipulating the function of splicing factors in the background of multiple forms of mutated TP53, to provide the foundation for future research that will lead to the development of more effective approaches to treat PDAC patients, improving their survival and quality of life.” Flyer Escobar-Hoyos CV
Leonard Alfredo Harris
Wednesday, October 10, Leonard Alfredo Harris, Vanderbilt University, 4:00 pm, 512 Light Hall: “Bet Hedging as a Survival Strategy in Complex Biological Systems and Cancer.”
Cells are complex, dynamic systems capable of initiating internal biochemical programs and adjusting their behavior in response to microenvironmental signals and stressors. Under the general term “phenotypic plasticity,” this phenomenon underlies important biological processes such as stem cell differentiation and epithelial-to-mesenchymal transitions. In bacteria, isogenic cell populations are known to exploit plasticity by phenotypically diversifying to increase their chances of survival to catastrophic external challenges, a strategy known as “bet hedging.” Recent evidence suggests that cancer cells may employ a similar strategy to survive the initial onslaught of anticancer therapeutics. Understanding the complex biochemical networks that underlie signal propagation and cell fate decisions is thus critical for improving treatments of various human diseases, including cancer. Here, I describe the biochemical basis for phenotypic plasticity within the framework of “Waddington landscapes,” present evidence for its role in anticancer drug resistance in non-small cell lung cancer and melanoma populations treated with targeted drugs, and discuss initial work toward constructing a detailed computational model of the biochemical machinery underlying cellular responses to external perturbations. Flyer CV
Thursday, May 3: Ishmail Abdus-Saboor, University of Pennsylvania, 4:00 pm, 512 Light Hall: “Genetic Interrogation of Neural Circuit Mechanisms for Pain.”
The nervous system is exquisitely tuned to mount the appropriate behavioral response to somatosensory stimuli ranging from a gentle caress to a harsh mechanical insult. How our nervous systems encode this information, from the level of sensory neuron activation in the skin up towards the central nervous system, in both normal and diseased states, remains enigmatic. We are working to uncover the mechanisms governing sensory encoding of touch, itch, and pain. Using optogenetics, quantitative analysis of animal behavior, and in vivo calcium imaging we have 1) determined how a population of pain-sensing neurons have unique morphological and physiological outputs depending upon body location, and 2) developed a new behavioral platform using high-speed videography, statistics, and machine learning to distinguish between innocuous versus painful behavior responses. Flyer CV Abdus-Saboor Lab
Thursday, March 1: Gustavo Silva, Duke University, 4:00 pm, 406 Preston Research Building: “K63 ubiquitin and the regulation of translation in response to oxidative stress.”
Ubiquitin is a prominent post-translational modification, which signals extensively beyond protein degradation. In this talk, Dr. Silva will present his research on how ubiquitin modifies ribosomes and controls cell resistance to stress. Flyer CV
Thursday, February 1: Dionna Williams, Johns Hopkins University, 4:00 pm, 512 Light Hall: “Beyond GPCR Recycling: B-Arrestin as a Neuroprotective Modulator of Innate Immune Responses.”
Thursday, December 14: Arion Kennedy, Vanderbilt University, 4:00 pm, 206 Preston Research Building: “CD8+ T Cells Regulate Liver Injury In Obesity-Related Nonalcoholic Fatty Liver Disease.”
The incidence of NAFLD has increased in Western countries due to the prevalence of obesity. Current interests are aimed at identifying the type and function of immune cells that infiltrate the liver and key factors responsible for mediating their recruitment and activation in obesity-associated NAFLD. Dr. Kennedy’s talk will focus on the role of CD8+ T cells in the development of obesity- associated NAFLD. Flyer CV
Avery Posey, Jr.
Thursday, November 16: Avery Posey, Jr., University of Pennsylvania, 12:00 pm, 898 Preston Research Building: “Accelerating CAR T Cells from the Model T to Driverless.”
October 5: Sade Spencer, Medical University of South Carolina, 4:00 pm, 206 Preston Research Building: “Dopaminergic Regulation of Relapse-Dependent Glutamatergic Plasticity.”
Dr. Spencer will present her modified cue-cocaine relapse model and the alterations in transient synaptic plasticity associated with relapse observed in the nucleus accumbens. She will also present newer data pertaining to the relationship between dopamine and glutamate during relapse, and how this impacts synaptic function. Flyer CV
April 13: Stephanie Correa, UCLA, 4:00 pm, 206 Preston Research Building: “Sex-Specific Neural Regulation of Energy Balance.”
March 16: Rene Raphemot, Duke University, 4:00 pm, 206 Preston Research Building: “A Genomic Screen Reveals New Host Factors Critical to Liver-Stage Malaria.”
Dr. Raphemot studies host-parasite interactions during the liver-stage of malaria infection. His goal is to understand host-related factors that are exploited by the parasite. Flyer Reporter Article Photos