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Hollfelder, D.

Publications and source records attributed to Hollfelder, D..

2 recordsLinked to original sources

Neural and Behavioral Adaptation to Listening with a Unilateral Cochlear Implant (CI)

The human auditory system must distinguish relevant sounds from noise. Severe hearing loss can be treated with cochlear implants (CIs), but how the brain adapts to electrical hearing remains unclear. This study examined adaptation to unilateral CI use in the first and seventh month after CI-activation using speech comprehension measures and electroencephalography (EEG) recordings, both during passive listening and an active spatial listening task. Neural phase-locking to amplitude-modulated (AM) sounds interacted with time, such that phase-locking longitudinally increased stronger for 40 compared with 4 Hz. In the spatial listening task, the benefit of performing the task with the CI on vs. off was most pronounced when the CI ear was primarily exposed to target speech. Lateralized alpha oscillations ([~]10 Hz) reliably marked CI users focus of spatial attention. Stronger alpha modulation in the hemisphere opposite to the non-implanted ear indicates an attentional bias toward the acoustically hearing ear. Our findings suggest that adaptation to hearing with a CI is accomplished by dynamic changes in auditory phase-locking and a bias in auditory spatial attention. Data availabilityAll data are available from the corresponding author upon request. A table including data for most important behavioural and neural outcome measures is available at https://osf.io/tkurz/.

neuroscience↗

Diversification of heart progenitor cells by EGF signaling and differential modulation of ETS protein activity

For coordinated circulation, vertebrate and invertebrate hearts require stereotyped arrangements of diverse cell populations. This study explores the process of cardiac cell diversification in the Drosophila heart, focusing on the two major cardioblast subpopulations: generic working myocardial cells and inflow valve-forming ostial cardioblasts. By screening a large collection of randomly induced mutants we identified several genes involved in cardiac patterning. Further analysis revealed an unexpected, specific requirement of EGF signaling for the specification of generic cardioblasts and a subset of pericardial cells. We demonstrate that the Tbx20 ortholog Midline acts as a direct target of the EGFR effector Pointed to repress ostial fates. Furthermore, we identified Edl/Mae, an antagonist of the ETS factor Pointed, as a novel cardiac regulator crucial for ostial cardioblast specification. Combining these findings we propose a regulatory model in which the balance between activation of Pointed and its inhibition by Edl controls cardioblast subtype-specific gene expression.

developmental biology↗