OpatzLab Developmental Neuroscience

Developmental neuroscience

The rhythm and melody of a piece of music is only conveyed successfully by an orchestra when each note is precisely timed, and when each instruments’ „voice“ is synchronized. The brain can also be considered an orchestra, with different brain regions representing „instruments“ and each neuron being a precisely time note. As in an orchestra, these components must coordinate their parts to create a meaningful „melody.“ Network oscillations have gained interest as an energy-efficient strategy for the organization and communication both within and between brain regions. In humans and animals oscillatory brain activity emerges very early in life, being already present in utero. While it is now known that these oscillations actively contribute to sensory perception and cognition in the adult brain, their function during development is still largely unknown.
Our group aims at elucidating the mechanisms underlying the maturation of neuronal networks under physiological and pathophysiological conditions. In particular, we assess the role of early network oscillations for the development of local and long-range communication in the brain in relationship with the emergence of cognitive behavior and multisensory perception. For this, we combine state-of-the-art electrophysiological methods and optogenetics with imaging and behavioral assessment. The following main topics are currently being investigated:

• Development of neuronal networks accounting for cognitive processing

• Dysfunction of neuronal networks and their early oscillations under pathological conditions (e.g. neuropsychiatric disorders, perinatal hypoxia-ischemia, perinatal stress)

• Sensory control of the maturation of cognitive processing

• Uni- and multisensory processing and ontogeny

• Development of neuro-immune cross talk and its role for pathologies later in life

Latest Publications

  • We are happy to share our latest publication in Brain, Behavior, and Immunity

    Cognitive deficits in neuropsychiatric disorders arise from disrupted neuronal network activity, and growing evidence implicates neuroinflammation in this process, though the underlying mechanisms remain unclear. Using the Df(16)A mouse model of the human 22q11.2 microdeletion, we found that early postnatal mice display altered inflammatory signaling and increased microglial density in superficial layers of the prefrontal […]read more

Open Positions

Newest Tweets

"our precision psychiatry approach: the biological definition of a subset of schizophrenia by identifying DISC1 protein aggregates, the generation of a corresponding animal model and a successful pharmacotherapy of a clinically relevant phenotype"

https://www.nature.com/articles/s41537-026-00729-y

Infantile #amnesia limits our recall of early-life memories, but what is its cellular basis?

@erikasstewart from @RyanLabTCD & @tcddublin reveals that #microglia regulate infant memory retrieval in mice during postnatal development.
@plosbiology.org 🧪

Opatz Lab
Developmental Neurophysiology