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Lobato-Rios, V.

Publications and source records attributed to Lobato-Rios, V..

4 recordsLinked to original sources

Object manipulation and affordance learning in Drosophila

Animals must manipulate objects to perform tasks like pushing away debris while navigating over complex, natural terrain. For previously unseen objects, efficient manipulation requires that their affordances--the possible actions one can perform upon them--first be learned through experience. However, the behavioral and neural mechanisms underlying the learning of object affordances remain largely unknown. To address this gap, we show that adult flies can learn to push small spherical objects without being given any explicit reward. To do this, flies appear to learn the balls pushability affordance: pushing is delayed when animals are first exposed to an immobile ball, and manipulating one ball accelerates pushing of a second one in a new context. Behavioral quantification of a largescale neural silencing screen reveals that specific visual projection neurons and olfactory sensory neurons regulate initial reactions to the object while dopaminergic neurons and circuits in the mushroom bodies, a center for associative learning and memory in insects, are critical for learning object affordances. These findings open the door to a mechanistic understanding of object manipulation and affordance learning.

neuroscience↗

Conspecific sociability is regulated by associative learning circuits

Sociability, an animals ease and propensity to interact with members of its own species, is a prerequisite for many important social interactions including courtship, mating, brood rearing, and collective behavior. Despite its fundamental nature, the manner through which sociability arises--whether it is innate or acquired and its neural mechanisms-- remains unknown. Here, we found that the fly, Drosophila melanogaster, produces a constellation of fearful reactions when it encounters another fly for the first time. However, these animals become sociable following several hours of exposure to conspecific (but not heterospecific) odors. Two large-scale neural silencing screens of 188 brain cell types revealed that both initial fearful reactions and learned sociability depend upon overlapping networks including circuits in the mushroom body, the principal center for associative learning and memory in the insect brain. Functional recordings of key mushroom body output neurons (MBONs) from this network over two hours of social interactions support a mechanistic model whereby fly odors modulate social valence by rebalancing MBON population activity, biasing action selection, and thereby driving sociable rather than fearful responses towards other flies. Thus, a center for learning and memory plays a fundamental role in establishing the basis for most social interactions.

neuroscience↗

Modeling conditional distributions of neural and behavioral data with masked variational autoencoders

Extracting the relationship between high-dimensional recordings of neural activity and complex behav- ior is a ubiquitous problem in systems neuroscience. Toward this goal, encoding and decoding models attempt to infer the conditional distribution of neural activity given behavior and vice versa, while dimensionality reduc- tion techniques aim to extract interpretable low-dimensional representations. Variational autoencoders (VAEs) are flexible deep-learning models commonly used to infer low-dimensional embeddings of neural or behavioral data. However, it is challenging for VAEs to accurately model arbitrary conditional distributions, such as those encountered in neural encoding and decoding, and even more so simultaneously. Here, we present a VAE-based approach for accurately calculating such conditional distributions. We validate our approach on a task with known ground truth and demonstrate the applicability to high-dimensional behavioral time series by retrieving the condi- tional distributions over masked body parts of walking flies. Finally, we probabilistically decode motor trajectories from neural population activity in a monkey reach task and query the same VAE for the encoding distribution of neural activity given behavior. Our approach provides a unifying perspective on joint dimensionality reduction and learning conditional distributions of neural and behavioral data, which will allow for scaling common analyses in neuroscience to todays high-dimensional multi-modal datasets.

neuroscience↗

Long-term imaging of the ventral nerve cord in behaving adult Drosophila

The dynamics and connectivity of neural circuits continuously change during an animals lifetime on timescales ranging from milliseconds to days. Therefore, to investigate how biological networks accomplish remarkable cognitive and behavioral tasks, minimally invasive methods are needed to perform repeated measurements, or perturbations of neural circuits in behaving animals across time. Such tools have been developed to investigate the brain but similar approaches are lacking for comprehensively and repeatedly recording motor circuits in behaving animals. Here we describe a suite of microfabricated technologies that enable long-term, minimally invasive optical recordings of the adult Drosophila melanogaster ventral nerve cord (VNC)--neural tissues that are functionally equivalent to the vertebrate spinal cord. These tools consist of (i) a manipulator arm that permits the insertion of (ii) a compliant implant into the thorax to expose the imaging region of interest; (iii) a numbered, transparent polymer window that encloses and provides optical access to the inside of the thorax, and (iv) a hinged remounting stage that allows gentle and repeated tethering of an implanted animal for two-photon imaging. We validate and illustrate the utility of our toolkit in several ways. First, we show that the thoracic implant and window have minimal impact on animal behavior and survival while also enabling neural recordings from individual animals across at least one month. Second, we follow the degradation of chordotonal organ mechanosensory nerve terminals in the VNC over weeks after leg amputation. Third, because our tools allow recordings of the VNC with the gut intact, we discover waves of neural population activity following ingestion of a high-concentration caffeine solution. In summary, our microfabricated toolkit makes it possible to longitudinally monitor anatomical and functional changes in premotor and motor neural circuits, and more generally opens up the long-term investigation of thoracic tissues.

neuroscience↗