Speaker: Dr. Ivan de Araujo, D.Phil from Yale University
Dr. de Araujo is an Associate Professor from Yale University in the John B. Pierce Laboratory. The goal of his lab is to define the sensorimotor circuitry that controls feeding programs. In 2008 work published in Neuron, Dr. de Araujo showed that taste alone is not enough to communicate the reward value of sugar; he knocked out the trpm5 taste receptor in mice to create a taste blind mouse, but found that mice still tend to prefer sugar after a few hours.
From there, he studied the brain regions that encode for this reward. He found that reward behavior can be abolished by inhibiting the mesolimbic and nigrostriatal brain dopamine pathways. He found that intake of sweeteners activates the ventral striatum while D-glucose activates the dorsal striatum, and that the infusion of nutrients into the gut increases dopamine levels proportional to the amount of calories infused. He then went about delineating the neural circuit driving this response.
Initially, he found that energy is transmitted to the substantia nigra pars compacta to the dorsal striatum to the substantia nigra. Meanwhile, sweetness, in the form of non-nutritive sweeteners, takes a different pathway; it is transmitted to the ventral tegmental area to the ventral striatum to the ventral pallidum. In summary, Dr. Ivan de Araujo has greatly impacted the way we understand the neurobiology of feeding and the reward pathways it elicits.
Speaker: Dr. Adam Gracz, Ph.D from UNC Chapel Hill
Title: “Stem Cell Dynamics in Intestinal and Biliary Epithelia.”
Dr. Gracz is an Assistant Professor at UNC Chapel Hill and started his independent laboratory in July 2016 after completing his postdoctoral fellowship in intestinal stem cell biology in Dr. Scott Magness’s lab at UNC Chapel Hill. His collective work has explored how cells pattern to form functional tissues.
In his post-doctoral work, Dr. Gracz studied how stemness is regulated in the intestine. He and his colleagues found that SOX9 EGFP is expressed in variable levels in intestinal crypts, specifically finding that the level of expression marks distinct cell populations including progenitor cells, intestinal stem cells, and enteroendocrine cells. They used various novel and state-of-the-art techniques in their work; specifically, they collaborated with biomedical engineers to use microraft arrays (MRAs) to facilitate genetic screening of organoids. After his successful postdoctoral fellowship, Dr. Gracz started his independent laboratory based on the central question “How does epigenetic regulation drive functional outcomes in cell and tissue biology?”
His lab focuses on two areas of research: the chromatin structure of intestinal stem cell biology and the cellular dynamics of biliary epithelium. In his talk, Dr. Gracz focused on his lab’s work in biliary epithelial populations. He is using SOX9 EGFP to study the sub-populations of biliary epithelial cells and to identify potential biliary stem cells. In summary, Dr. Gracz is continuing to further the field’s understanding of stem cell dynamics in GI epithelial tissues.
Jack Odle, Ph.D.
William Neal Reynolds Distinguished Professor
Department of Nutrition
North Carolina State University
Dr. Odle Lab studies lipid metabolism, specifically of long chain fatty acids found in milk, and intestinal disorders, specifically ischemic or infectious insults. His group uses piglets as a pediatric nutrition model and has discovered the mechanisms by which several fatty acids, like arachachidonic acids, stimulate the repair of the intestinal epithelium to maintain intestinal health. These findings have served as a foundation to develop human infant formulas.
Jonathan Campbell, Ph.D.
Assistant Professor of Medicine
Dr. Campbell studies glucose-dependent insulinotropic peptide (GIP), an incretin hormone released from the proximal small intestine that stimulates insulin release after a meal.
The field of incretin biology has long focused on the other incretin, glucagon-like peptide-1 (GLP-1), and utilized this hormone as a pharmaceutical target for diabetes and obesity. GIP, however, is less well understood; previous studies demonstrate that GIP resistance and receptor loss is associated with decline in pancreatic beta cell function, as seen in type II diabetes. Dr. Campbell’s laboratory is working to uncover the mechanism and effects of GIP.
Using global GIP receptor knockouts, he has shown that beta cells without GIPR are more sensitive to the other incretin, GLP-1, and maintain the ability to secrete insulin. Dr. Campbell is creating tissue-specific knockout models to describe beta cell defects seen in his transcription factor knockout experiments. His goal is that these experiments may serve as a target for diabetes pharmaceuticals.
Staci Bilbo, Ph.D.
Associate Professor of Psychology and Neuroscience
Dr. Bilbo’s laboratory explores the interactions between the nervous and immune systems. In particular, their interest is how nerves and immune cells join forces to influence behaviors such as cognition and emotion. Recent studies have linked the immune system with a number of neurodevelopmental disorders, such as schizophrenia, anxiety/depression, and autism.
Dr. Bilbo’s research focuses on how early challenges in life, such as infections, prime the immune system to influence brain development and affective behaviors. She is now the Director of the Lurie Center for Autism at Harvard Medical School.
Praveen Sethupathy, Ph.D.
Assistant Professor of Genetics
Dr. Praveen Sethupathy studies microRNAs and how they respond to gut microbes.
Here is a short recap from his talk:
- Non-coding RNA encompasses a large class of RNA, including microRNA. The Sethupathy lab in interested in how miRNA regulate diseases, can act as biomarkers of disease, and how they respond to changes in environment.
- Sethupathy lab has studied how miRNA is related to Diabetes and Obesity, but recent RNA sequencing data has turned their attention to miRNA in the GI system and their relationship to Microbiota
- Their hypothesis is that miRNA respond to the microbiota, this response is cell-type specific and that miRNA can control Enteroendocrine cells
- They have mapped miRNA in intestinal epithelial cells and have seen that in GI stem cells, there is increased miR-30d, miR-92, miR-7, miR-375, and let-7, while miRNA-375 is increased in microbiota-sensitive stem cells
- An ex vivo knockout of miR-375 using LNA 375 led to proliferation of EECs
- In conclusion, miRNA are specific to cell types in the GI epithelium, miRNA are more sensitive in stem cells than in other GI cells, and a sub-population analysis of miRNA is needed to check response to microbiota.
Xiling Shen, Ph.D.
Associate Professor of Biomedical Engineering
Dr. Shen’s laboratory recently moved from Cornell University and has developed a unique 3D printed scaffold to image the gut in awake behaving animals. The device can be used to image from stem cells, to bacteria, to neurons. His team is also working on peripheral nerve stimulation and recording devices for nerves innervating the gut.
This story was highlighted as one of the top 100 stories by Discovery Magazine in 2016
Ian Carroll, Ph.D.
Assistant Professor of Medicine at UNC-Chapel Hill
Dr. Carroll’s research studies how intestinal microbes influence gut physiology and behaviors. Dr. Carroll also uses high throughput sequencing of bacterial genes to characterize the enteric microbiota in human subjects with gastrointestinal disease and mouse models of intestinal inflammation. His goal is to develop enteric microbial-based therapies for the treatment of gut diseases.
In germ free conditions, mice have enlarged cecums, blunted villi, and less weight gain per calories consumed. These changes reverse after inoculation. Microbiota influences emotional state in a complex fashion and germ free mice have higher stress and lower anxiety. Stress increases or decreases depending on the species of bacteria added. Emotional changes after inoculation of germ free mice are not observed when the vagus is severed.
In starvation states, as seen in anorexia, microbiota diversity decreases and the relative proportions of species change. These changes appear to perpetuate symptoms in anorexia. A single case study showed fecal transplant leading to weight gain in a human subject and such interventions might have therapeutic potential in the future.
Janelle Arthur, Ph.D.
Assistant Professor of Microbiology and Immunology
UNC-Chapel Hill School of Medicine
Janelle’s group seeks to understand how inflammation alters the pro-carcinogenic capabilities of the microbiota, with the long-term goal of targeting resident microbes as a preventative and therapeutic strategy to lessen inflammation and reduce the risk of colorectal cancer.
They are focus on clinical strains of intestinal E. coli isolated directly from human inflammatory bowel disease (IBD) patients, who are known to experience a high risk of colorectal cancer. Janelle’s goal is to uncover novel microbial targets will enable us to manipulate the intestinal microbiota as a therapeutic target for human digestive diseases and cancer.