Search bioRxiv⌕ Search

Biology subjects

Foltz, M.

Publications and source records attributed to Foltz, M..

2 recordsLinked to original sources

Visual object recognition in the fly: the internal representation of a predator drives defensive behaviour

Animals recognize visual objects and respond to them appropriately to survive. This process is thought to unfold in stages: the visual scene is first deconstructed into constituent features, which are then reconstructed into representations of object identity and relayed to motor circuits. Here we define a neural circuit in Drosophila that underlies the visual recognition of a natural predator, the parasitoid wasp, and orchestrates defence. We found that flies exhibit a repertoire of directed defensive actions structured by the wasp's position within the fly's field of view. Expression of these behaviours is driven by visual detection of a conspicuous morphological cue -- the wasp's elongated antennae. A small subset of lobula columnar (LC) visual projection neuron types are required for defence and are activated by constituent visual features of the wasp. Three LC types respond selectively to the wasp's antennae, and relay this information to LC9, which sums antennal- and body-feature signals to form a composite representation of the wasp. Spatial filtering of this representation onto a descending premotor pathway translates the wasp's location in visual space into directed defence. Feature combination followed by spatial filtering may constitute a general mechanism for coupling object identity to context-appropriate action.

neuroscience↗

Effect of selective lesions of nucleus accumbens μ-opioid receptor-expressing cells on heroin self-administration in male and female rats: a study with novel Oprm1-Cre knock-in rats

The brain {micro}-opioid receptor (MOR) is critical for the analgesic, rewarding, and addictive effects of opioid drugs. However, in rat models of opioid-related behaviors, the circuit mechanisms of MOR-expressing cells are less known because of a lack of genetic tools to selectively manipulate them. We introduce a CRISPR-based Oprm1-Cre knock-in transgenic rat that provides cell-type specific genetic access to MOR-expressing cells. After performing anatomical and behavioral validation experiments, we used the Oprm1-Cre knock-in rats to study the role of nucleus accumbens (NAc) MOR-expressing cells in heroin self-administration in male and female rats. Using RNAscope, autoradiography, and fluorescence in situ hybridization chain reaction (HCR-FISH), we found no differences in Oprm1 expression in NAc, dorsal striatum (DS), and dorsal hippocampus, or MOR receptor density (except DS) or function between Oprm1-Cre knock-in rats and wildtype littermates. HCR-FISH assay showed that iCre is highly co-expressed with Oprm1 (95-98%). There were no genotype differences in pain responses, morphine analgesia and tolerance, heroin self-administration, and relapse-related behaviors. We used the Cre-dependent vector AAV1-EF1a-Flex-taCasp3-TEVP to lesion NAc MOR-expressing cells and report sex-specific effects: the lesions decreased acquisition of heroin self-administration in male Oprm1-Cre rats and had a stronger inhibitory effect on the effort to self-administer heroin in female Oprm1-Cre rats. The validation of an Oprm1-Cre knock-in rat enables new strategies for understanding the role of MOR-expressing cells in rat models of opioid addiction, pain-related behaviors, and other opioid-mediated functions. Our initial mechanistic study with these rats suggests a sex-specific role of NAc MOR-expressing cells in heroin self-administration. Significance statementThe brain {micro}-opioid receptor (MOR) is critical for the analgesic, rewarding, and addictive effects of opioid drugs. However, in rat models of opioid-related behaviors, the circuit mechanisms of MOR-expressing cells are less known because of a lack of genetic tools to selectively manipulate them. We introduce a CRISPR-based Oprm1-Cre knock-in transgenic rat that provides cell-type specific genetic access to brain MOR-expressing cells. After performing anatomical and behavioral validation experiments, we used the Oprm1-Cre knock-in rats to show a potential sex-specific role of nucleus accumbens MOR-expressing cells in heroin self-administration. The new Oprm1-Cre rats can be used to study both the general and sex-specific role of brain MOR-expressing cells in animal models of opioid addiction, pain-related behaviors, and other opioid-mediated functions.

neuroscience↗