Research Areas
Neurotransmitter and neurotrophin receptors and cell signaling; learning, memory and synaptic plasticity; ion channels, synaptic function, neurodevelopment and developmental disabilities






Dr. Lucas Pozzo-Miller completed his university studies in Biology (1986) and earned his Doctorate in Biology (1989), both from the Universidad Nacional de Córdoba, Argentina. He trained as postdoctoral fellow at Case Western Reserve University, Cleveland OH (1990-1992), and at the former Roche Institute of Molecular Biology, Nutley NJ (1992-1995). Dr. Pozzo-Miller performed summer research at the Marine Biological Laboratory, Woods Hole MA (1994 Grass Foundation Fellow and 1995 Lakian Foundation Fellow), and was a Senior Staff Fellow at NINDS, NIH, Bethesda MD (1995-1998). Dr. Pozzo-Miller joined the Department of Neurobiology at the University of Alabama at Birmingham in 1998, and is currently Professor of Neurobiology.

Research Interests

The long-term interest of the Pozzo-Miller lab is to characterize the functional role of structurally defined neuronal compartments such as dendritic spines and presynaptic terminals, and how they participate in synaptic development, function and plasticity as they relate to learning and memory. We focus on the hippocampus due to its well-known role in learning and memory.

Neurotrophins such as brain-derived neurotrophic factor (BDNF) are secretory proteins that regulate neuronal survival and differentiation, as well as synapse development, function and plasticity. Neurotrophic factors are strong candidates to provide the molecular signaling pathways mediating complex interactions leading to appropriate dendritic maturation and synapse development. We focus on the actions of neurotrophins in the hippocampus to characterize the regulation of synaptic transmission and plasticity by slow-acting non-classical neuromodulators. Currently, we are investigating the “BDNF hypothesis” of Rett syndrome, a neurodevelopmental disorder associated with autistic features and intellectual disabilities that is caused by mutations in MECP2, a transcriptional regulator of many genes, including Bdnf. In our studies, we apply several functional and structural approaches to cultured neurons and acute and cultured slices of hippocampus, including intracellular recordings, Ca2+ and voltage-dye imaging, confocal microscopy, multiphoton excitation microscopy, as well as conventional and rapid-freezing electron microscopy.


Graduate School
Ph.D., Universidad Nacional de Córdoba, Argentina