Beth Stevens is an associate professor at Harvard Medical School in the FM Kirby Neurobiology Research Center at Boston Children’s Hospital, and an institute member of the Broad Institute.
Her research seeks to understand the mechanisms that regulate the development and elimination of synapses by focusing on how microglia and immune-related molecules mediate this process.
Beth received her Ph.D. in Neuroscience in 2003 at the University of Maryland, College Park. She performed her dissertation research at the National Institutes of Health (NICHD) in the area of neuron-glia interactions. In her postdoctoral work with Ben Barres at Stanford University, she discovered that the classical complement cascade, part of the innate immune system, helps to mediate developmental CNS synapse elimination. Their findings have raised many questions about how the complement cascade normally works to eliminate synapses and especially whether it becomes abnormally reactivated in brain diseases such as AD that impair synaptic connectivity.
In 2008, Dr. Stevens established her independent laboratory in the FM Kirby Neurobiology Center at Children’s Hospital where she is currently using a combination of molecular, physiological and high resolution imaging techniques to dissect the mechanisms by which microglial cells and immune –related molecules (ie.complement, cytokines) regulate synapse function during health and disease. She is investigating the mechanisms that drive synapse loss and dysfunction in AD, Huntington’s disease, as well as neurodevelopmental disorders, such as autism and schizophrenia. Beth is a recipient of several young investigator awards, including: Ellison Medical Foundation New Scholar in Aging, John Merck Scholar (2011), Presidential Early Career Award for Scientists and Engineers (PECASE), and a 2015 MacArthur Fellow Award.
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