Daniela Schiller
Daniela Schiller is a neuroscientist who leads the Affective Neuroscience Lab at the Mount Sinai School of Medicine. She is best known for her work on memory reconsolidation, and on modification of emotional learning and memory.
Early life and education
Schiller was born in Rishon LeZion, Israel. She is the daughter of a Moroccan mother and a Ukrainian father. Schiller's father, Sigmund Schiller, is a survivor of the Holocaust. Schiller is the youngest of four children. She received a bachelor's degree in psychology and philosophy in 1996, and her doctorate in psychobiology from Tel Aviv University in 2004. She was awarded a Fulbright fellowship and worked with Elizabeth A. Phelps and Joseph E. LeDoux at New York University. Schiller plays drums and sings backing vocals for The Amygdaloids and Supersmall.Awards and recognition
- 2014 Klingenstein-Simons Fellowship in Neuroscience
- 2013 Kavli Frontiers of Science Fellow, National Academy of Sciences
- 2010 Blavatnik Award for Young Scientists
- 2005 Fulbright Scholar
Scientific research
The goal of Schiller's research is to unravel the neurocognitive mechanisms that make emotional memories malleable, allowing for memory modification and for the adaptive adjustment of emotional and social behavior.Research on the modulation of fear learning
Schiller's research addressed this question by using a behavioral paradigm called reversal learning in conjunction with physiological skin conductance measurements and neuroimaging. In this task, subjects first learned to associate one of two neutral stimuli with an aversive outcome, and then had to flexibly modify this learning when the second stimulus began to predict the aversive outcome, while the initial predictive stimulus ceased to do so. The study found that responses in the amygdala and the striatum flexibly tracked the predictive aversive value of the conditioned stimuli, and switched their responses from one stimulus to another when reversal occurred. The ventromedial prefrontal cortex also participated albeit in the opposite direction, showing stronger responses to the safe stimuli, but also dissociating 'naïve' safe stimuli from stimuli that used to be dangerous but are now safe. In order to identify a general mechanism underlying fear modulation regardless of the particular strategy used, Schiller and Mauricio Delgado demonstrated the overlapping neural systems mediating extinction, reversal and regulation of learned fear. Further research used the reversal learning data to dissociate the different computations performed by the striatum and amygdala during fear learning. The reversal protocol also helped identifying differences between combat veterans with or without a PTSD diagnosis in how they compute prediction error and update the value of fear predictive stimuli, and the neural tracking of these computations. Schiller's investigation was extended also to instrumental learning of active avoidance, revealing the neural mechanisms that predict successful active coping with threats in the human brain.Research on memory reconsolidation
To examine the ability to modify emotional memory, Schiller's research focused on reconsolidation, which is a memory process of restabilizing a destabilized memory. Reconsolidation can be blocked using pharmacological agents, or non-invasive behavioral interference such as new motor learning during the reconsolidation of motor memories, new episodic learning during reconsolidation of declarative memory, and extinction learning during the reconsolidation of fear memory. Schiller's research demonstrated the interference of reconsolidation of fear memory using extinction in humans. One failure to reproduce this latter finding in an independent study or to validate the article's claims using the original data have cast doubts on whether it can be replicated. However, the authors contend that it is valid, the original data is publicly available and replicates, and of subsequent replications, about 80% were successful.Additional research demonstrated retrieval-extinction interference in mice, rats, and humans. Additional demonstrations of retrieval-extinction were shown in juvenile rats and adolescents humans. Variations of the effect include retrieval followed by vicarious extinction and imaginal extinction. The retrieval-extinction procedure was also effective in clinical populations, including heroine addicts, tobacco smokers, PTSD and spider phobics with long-lasting effects. Some forms of therapy, such as coherence therapy, are built on the principles of memory reconsolidation and are designed to maximally optimize this process. Studies have also demonstrated engram specific manipulation of retrieval-extinction on remote memories. The Epigenetic priming of behavioral memory updating was shown to enable retrieval-extinction interference. Additional conceptual replications and demonstrations of reconsolidation updating using other forms of behavioral and non-invasive interferences have been reported. Some studies failed to replicate retrieval-extinction effects and disputed the results. Theoretical formulations and empirical work suggest that inconsistencies in reconsolidation effects may depend on the degree of memory destabilization, as not every memory recall involves neural destabilization; or on the efficacy of the interference, which could differ across individuals and populations.