Postdocs

Research Interest: Neural Stem Cell biology, cortical development and RNA regulation. Neural stem cells (NSCs) generate a remarkable diversity of neurons and glial cells during development of the cerebral cortex and defects in progenitor proliferation and differentiation are a major cause of neurodevelopmental disorders such as microcephaly, autism, seizures and intellectual disability. RNA-binding proteins (RBPs) are involved in post-transcriptional regulation and mRNA metabolism and have recently emerged as critical regulators of NSCs during cortical development. In April 2017, I joined Dr. Debra Silver´s lab where I plan to study the role of RBP in neurogenesis during cortical development and the regulation of RNA and signaling in neural progenitors. I will use multidisciplinary approaches that include In Utero Electroporation, progenitor primary cultures, brain slices, transgenic mice, biochemical assays and transcriptomic/translational profiles. Background: I am from Argentina and I did my graduate training in Dr. Gustavo Paratcha´s lab in the Institute of Cellular Biology and Neuroscience “Prof. E. De Robertis” (IBCN) in the University of Buenos Aires (UBA – CONICET), Argentina. My PhD thesis focused on the negative regulation of neurotrophic factor receptor signaling in developing neurons. Personal Interests: In my free time I really enjoy hiking, playing soccer, going out with friends and family, traveling around, reading and watching series and movies.

I have a background in retinal gene therapy, developing a treatment for an animal model of an inherited retinal disease and engineering novel AAV capsid variants. Currently, I study retinal circuitry functionality both in healthy tissue and models of degenerative retinal disease. In particular, I want to understand how different bipolar cell types shape visual processing, and how that processing is impaired once connectivity between photoreceptors and bipolar cells is lost in advanced forms of disease.

Despite my graduate training as a biomedical engineer, I’m interested in deciphering the physiological roles of membrane-bound ion channels and lipid transporters. Currently I’m focusing on understanding the physiological functions of the newly discovered TMEM16 protein family, which is consisted of calcium-activated chloride channels and calcium-dependent phospholipid scramblases. TMEM16-mediated chloride transport and phospholipid scrambling are involved in many important cellular processes, and the members have already been linked to several devastating diseases, including cerebellar ataxia, muscular dystrophy and scott syndrome. My current long-term goal is to elucidate the molecular underpinnings how TMEM16 ion channels and lipid scramblases play a role in both nervous and peripheral systems, and especially how their cellular functions are implicated in human health and disease.