{"id":28662,"date":"2024-03-05T16:44:23","date_gmt":"2024-03-05T21:44:23","guid":{"rendered":"https:\/\/biology.mit.edu\/?page_id=28662"},"modified":"2024-08-23T15:13:39","modified_gmt":"2024-08-23T19:13:39","slug":"mit-biology-catalyst-symposium","status":"publish","type":"page","link":"https:\/\/biology.mit.edu\/about\/diversity\/mit-biology-catalyst-symposium\/","title":{"rendered":"MIT Biology Catalyst Symposium"},"content":{"rendered":"
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In 2022, the department launched the MIT Biology Catalyst Symposium with leadership from the Faculty DEI Committee and DEI Officer. \u00a0This symposium is part of a new effort to bring outstanding postdocs from traditionally underrepresented backgrounds in science to engage with members of our community. Aimed specifically at postdocs pursuing academic careers, the three-day symposium provides a venue for participants to share their research, discuss exciting new directions, and make new professional connections. We will welcome eight Catalyst Fellows to campus for the second symposium in April of 2024, which is co-sponsored by The Picower Institute for Learning and Memory.<\/p>\n
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\n <\/td>\n <\/td>\n <\/td>\n<\/tr>\n \n <\/a><\/p>\n
Chlo\u00e9 Baron (she\/her)<\/p>\n<\/td>\n
“Apelin-mediated clonal expansion of niche endothelial cells drives selection of leukemic and normal HSC clones.”<\/td>\n Chlo\u00e9 did her PhD in the lab of Alexander van Oudenaarden at the Hubrecht Institute in the Netherlands. There, she developed novel single-cell tools for machine-learning assisted flow cytometry sorting, transcriptome profiling and CRISPR-Cas9-based genetic lineage tracing. She benchmarked and applied these technologies to the mouse and zebrafish hematopoietic system and unraveled the transcriptome and clonality of hematopoietic stem and progenitor cells during embryonic development and adulthood. For her postdoctoral training, Chlo\u00e9 joined the lab of Leonard Zon at Boston Children’s Hospital where she extended her use of genetic lineage tracing to characterize the clonal dynamics of the HSC niche at steady state and upon leukemia. Her work identified a clonal response of niche cells in leukemic marrows and the cellular mechanisms responsible for selective clonal amplification of niche endothelial cells to support disease progression.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Maria Cec\u00edlia Canesso (she\/her)<\/p>\n<\/td>\n
“Intercellular communication determining fates in the intestinal mucosa”<\/td>\n Maria Cec\u00edlia Canesso received her PhD in Immunology from Federal University of Minas Gerais in Brazil. She is a postdoctoral researcher at The Rockefeller University investigating how immune cells in the intestine decide whether to promote tolerance or induce an inflammatory response to food and the commensal microbiota. To answer this question, she developed the application of a novel technology, the LIPSTIC (Labeling Immune Partnerships by SorTagging Intercellular Contacts), in the intestine, which enabled tracking of cell-cell interactions in vivo. Maria Cecilia was awarded a Pew Latin American Fellowship and received the K99 Pathway to Independence Award.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Kiara Eldred (she\/her)<\/p>\n<\/td>\n
“Visualizing progenitor cell trajectories in the developing human retina”<\/td>\n Dr. Eldred received her undergraduate degree in Biochemistry from the University of Washington where she worked in the laboratory of Richard Palmiter. She went on to complete her PhD at Johns Hopkins University in Cellular, Molecular, Developmental Biology and Biophysics. There she trained in the labs of Robert Johnston and Samer Hattar studying photoreceptor cell fate specification in the human retina. She was awarded an HHMI Gilliam Fellowship and an NSF fellowship during her graduate studies. Her thesis was recognized with the receipt of the Weintraub Graduate Student Award. Currently Dr. Eldred is a postdoctoral fellow in the laboratory of Thomas Reh at the University of Washington, studying cell fate specification, tumorigenesis, and regeneration in the human retina. In this position, she has been awarded a Damon Runyon-Sohn Pediatric Cancer Fellowship as well as an HHMI Hanna Gray Fellowship.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Caitlin Kowalski (she\/her)<\/p>\n<\/td>\n
“Interkingdom interactions of the skin microbiome”<\/td>\n Caitlin Kowalski is a Helen Hay Whitney Postdoctoral fellow at the University of Oregon in the lab of Matthew Barber. She received her PhD in Microbiology and Immunology in 2020 from the Guarini School of Graduate Studies at Dartmouth under the mentorship of Robert Cramer. Her dissertation investigated how oxygen availability impacts pathogenesis and antifungal susceptibility of the human fungal pathogen Aspergillus fumigatus.<\/em> Building upon her interests in how fungi influence human health, Caitlin\u2019s postdoctoral research focuses on how skin resident fungi interact with bacterial pathogens to impact host health and pathogen evolution. In 2023, Caitlin was awarded a L\u2019Or\u00e9al USA For Women in Science Fellowship and selected as a Leading Edge Fellow.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Fabi\u00e1n Morales-Polanco (he\/him)<\/p>\n<\/td>\n
“Spatial and temporal subcellular interactomics reveal factors differentially recruited to nuclear and cytosolic spatial protein quality control”<\/td>\n Fabi\u00e1n Morales-Polanco, PhD, is a postdoctoral scholar at Stanford University’s Frydman Lab, specializing in proteostasis in eukaryotic cells. His focus lies in translation, clearance mechanisms, and their implications for health and disease. He holds a Ph.D. in Biotechnology and Enterprise from the University of Manchester, UK. Fabi\u00e1n’s research in RNA biology, protein quality control, and aging-related molecular mechanisms has yielded notable discoveries. He has investigated nuclear and cytoplasmic protein quality control interactions and novel pathways for clearing misfolded proteins. His work also encompasses studying the co-localization and translation of glycolytic mRNAs within RNA granules, unveiling regulatory mechanisms for protein complex assembly. Dedicated to scientific communication and mentorship, Fabi\u00e1n strives to inspire students’ enthusiasm for scientific inquiry while advancing proteostasis research for the betterment of human health.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Kali Pruss (she\/her)<\/p>\n<\/td>\n
“Multi-system responses to intergenerational transmission of small intestinal bacteria from undernourished Bangladeshi children and women with enteropathy”<\/td>\n Kali Pruss, PhD, has spent her research career thus far exploring the hypothesis that the nature of inflammation dictates the nature of interactions between the gut microbiota and host. As an undergraduate in Ron Taylor\u2019s lab, she focused on understanding Vibrio cholerae <\/em>motility towards chemo-attractants present in both the gut and environmental reservoirs. During her PhD in Justin Sonnenburg\u2019s lab, she teased apart mechanisms by which gut bacteria alter their metabolic behavior depending on the extent of inflammation in the gut, with a focus on the enteric pathogen, Clostridioides difficile. <\/em>She discovered a metabolic pathway that the organism uses to exploit a host-derived metabolite produced during inflammation as well as one it turns to for persistence in the absence of inflammation. A related gut commensal, Clostridium sporogenes<\/em>, rather than utilizing host compounds, produces aromatic amino acid metabolites that the host can use for energy generation through fatty acid \u00df-oxidation.<\/p>\n Currently, during her post-doc in Jeffrey Gordon\u2019s lab, she is working to understand how the small intestinal microbiota mediates the chronic inflammatory state that accompanies environmental enteric dysfunction (EED) and the systemic effects of this state. As the etiological agents of EED are undefined, she\u2019s employing a top-down approach: starting with duodenal aspirates from children or adult Bangladeshi women with EED, she has developed gnotobiotic mouse models to understand the effect of members of the small intestinal microbiota on intestinal physiology, the immune system, brain biology, and fetal development. She plans to start an independent career investigating interactions between the environment, gut microbiota, and fetal development.<\/td>\n<\/tr>\n
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Rodrigo Romero (he\/him)<\/p>\n<\/td>\n
\u201cThe role of lineage plasticity and its impact on the tumor microenvironment during therapy resistance.\u201d<\/td>\n Rodrigo was born in Caracas Venezuela. He obtained his BSc in Biology from Suffolk University, and a PhD in Biology from the Massachusetts Institute of Technology (MIT). As a PhD student with Tyler Jacks, he was among the first to use CRISPR to interrogate genotype-specific dependencies in lung cancers harboring KEAP1<\/em> mutations. As a Charles. H. Revson Fellow with Charles Sawyers at Memorial Sloan Kettering Cancer Center, he developed novel models of prostate cancer used to unravel the mechanisms underlying resistance to androgen-deprivation therapy through lineage plasticity.<\/td>\n<\/tr>\n \n <\/a><\/p>\n
Zuri Sullivan (she\/her)<\/p>\n<\/td>\n
“How infection makes us sick: neuroimmune control of sickness behavior”<\/td>\n Zuri is an HHMI Hanna H. Gray Fellow in the lab of Dr. Catherine Dulac in the Department of Molecular and Cellular Biology at Harvard University. An immunologist and molecular neuroscientist, she focuses on the neuroimmune interactions that govern sickness behavior during infection. Zuri earned an AB in Molecular and Cellular Biology from Harvard University, where she developed an interest in host pathogen interactions while working in Dr. Eric Rubin\u2019s lab at the Harvard School of Public Health. After college, she spent two years working in Durban, South Africa as a Fulbright Scholar, studying human immunity to tuberculosis and HIV. She earned a PhD in Immunobiology from Yale University, where she worked in the lab of Dr. Ruslan Medzhitov as an NSF Graduate Research Fellow. There, she discovered an unexpected role for the immune system in the control of nutrient uptake in the intestine. After graduate school, Zuri changed fields to pursue postdoctoral training in molecular neuroscience, where she studies the impact of inflammatory signals on neural circuits that control social interaction. Zuri\u2019s long-term research interests aim to bridge immunology and neuroscience to understand the molecular and cellular mechanisms underlying sickness behavior.<\/td>\n<\/tr>\n \n \n \n<\/td>\n
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\nAgenda<\/h2>\n
April 28th<\/h3>\n
6:00 pm:\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Dinner with Catalyst Fellows and faculty hosts<\/p>\n
April 29th\u00a0<\/em><\/h3>\n
All talks on April 29th will take place in the Whitehead Institute McGovern Auditorium.<\/p>\n
9:05-9:15 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Welcome\/opening remarks<\/p>\n
9:15-9:45 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Maria Cec\u00edlia Canesso<\/p>\n
9:50-10:20 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Zuri Sullivan<\/p>\n
10:25-10:55 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Kiara Eldred<\/p>\n
10:55-11:15 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Break<\/p>\n
11:15-11:45 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Caitlin Kowalski<\/p>\n
11:50 am-12:20 pm\u00a0 \u00a0 Rodrigo Romero<\/p>\n
12:20-1:20 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Lunch with post-docs, trainees, and faculty<\/p>\n
1:30-2:00 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Chlo\u00e9 Baron<\/p>\n
2:05-2:35 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Kali Pruss<\/p>\n
2:40-3:10 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Fabi\u00e1n Morales-Polanco<\/p>\n
3:10-3:30 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Break<\/p>\n
3:30-5:00 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a01:1 Meetings with Catalyst Fellows and faculty<\/p>\n
5:00-6:00 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Break<\/p>\n
6:00-9:00 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Dinner with Catalyst Fellows and faculty<\/p>\n
April 30th<\/h3>\n
9:30-11:00 am\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a01:1 Meetings with Catalyst Fellows and faculty<\/p>\n
11:15am-12:15 pm\u00a0 \u00a0 \u00a0 \u00a0Panel for Catalyst Fellows and invited postdocs on Faculty Search process<\/p>\n
12:15-1:00 pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 Lunch with Biology post docs and graduate students<\/p>\n
1:00-2:00pm\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Panel for Catalyst Fellows and invited postdocs about Junior Faculty experience<\/p>\n
Symposium concludes<\/p>\n
Previous MIT Biology Catalyst Symposia<\/h2>\n