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Bermedo-Garcia, F.

Publications and source records attributed to Bermedo-Garcia, F..

2 recordsLinked to original sources

Sticking the landing: leg mechanosensory feedback coordinates the transition from flight to landing

Landing is an especially demanding stage of flight. Flying animals must rapidly transform multimodal sensory information into the coordinated movement of multiple limbs in order to transition from flight to a stable standing posture, often on surfaces that vary in stability, texture, and orientation. Failure to do so can be costly, leading to injury or death. Here, we examine the role of mechanosensory feedback in guiding landing in the fruit fly, Drosophila melanogaster. We describe a novel behavioral assay in which we deliver localized mechanical contact to individual legs of tethered, flying flies while simultaneously quantifying their three-dimensional behavioral kinematics. We find that mechanical contact of the distal legs reliably induces flight cessation, and initial leg contact triggers distinct patterns of inter-leg coordination. Recruitment of subsequent leg contacts predicts landing likelihood, suggesting that coordinated feedback from multiple legs reinforces the landing transition. Next, we combine synapse-resolution connectomes with optogenetic manipulations to identify the mechanosensory pathways underlying these behaviors. Finally, we describe a population of inhibitory ascending neurons that integrates mechanosensory input from the legs and facilitates the transition from visually-mediated landing initiation to touch-mediated flight cessation. Overall, our results reveal an important set of neural circuits that convert local tactile feedback into a coordinated, rapid behavioral state transition.

neuroscience↗

Control of mammalian brain aging by the unfolded protein response (UPR)

Aging is the major risk factor for the development of dementia and neurodegenerative disorders, and the aging brain manifests severe deficits in buffering capacity by the proteostasis network. Accordingly, we investigated the significance of the unfolded protein response (UPR), a major signaling pathway that copes with endoplasmic reticulum (ER) stress, to normal mammalian brain aging. Genetic disruption of ER stress sensor IRE1 accelerated cognitive and motor dysfunction during aging. Exogenous bolstering of the UPR by overexpressing an active form of the transcription factor XBP1 restored synaptic and cognitive function in addition to reducing cell senescence. Remarkably, proteomic profiling of hippocampal tissue indicated that XBP1s expression corrected age-related alterations in synaptic function. Collectively, our data demonstrate that strategies to manipulate the UPR sustain healthy brain aging. One Sentence SummaryThe IRE1/XBP1 pathway dictates when and how brain function declines during aging.

neuroscience↗