Illuminating Neuronal-Astrocytic Pathways for Sleep homeostasis

Informacje na temat projektu

iNAPS

Identyfikator umowy o grant: 715933

DOI

10.3030/715933

Projekt został zamknięty

Data podpisania przez KE 16 Grudnia 2016

Data rozpoczęcia 1 Kwietnia 2017

Data zakończenia 31 Marca 2023

Finansowanie w ramach

• EXCELLENT SCIENCE - European Research Council (ERC)

Koszt całkowity

€ 1 500 000,00

Wkład UE

€ 1 500 000,00

Koordynowany przez

HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH
Germany

Periodic Reporting for period 4 - iNAPS (Illuminating Neuronal-Astrocytic Pathways for Sleep homeostasis)

Okres sprawozdawczy: 2021-10-01 do 2023-03-31

Podsumowanie kontekstu i ogólnych celów projektu

ERC iNAPS 715933 aimed to discern the mechanisms controlling sleep homeostasis. In other words, to understand how the brain senses the need for sleep and drives appropriate sleep patterns. Most people know what sleep deprivation feels like, yet the impact of significant sleep loss on health, safety, and the economy is underappreciated. We believe that if we can understand the brain circuits functioning in sleep deprivation and governing sleep drive, we can devise ways to augment them, enabling more restorative sleep and all the beneficial health, safety, and economic benefits that ensue.

The overall objectives were: 1) identify the cell types and brain regions involved in sleep homeostasis; 2) determine how these cells affect sleep drive; and 3) evaluate the role of astrocytes, a special type of brain cell, in sleep homeostasis.
In the course of the action, we achieved the main objectives, gaining understanding of the cellular basis of sleep homeostasis and laying the foundation for future work in this area.

Prace wykonane od początku projektu do końca okresu sprawozdawczego oraz najważniejsze dotychczasowe rezultaty

We Identified a molecularly defined population of neurons in the brain’s amygdala, a region often associated with emotion, that are activated by sleep deprivation. We manipulated their activity to reveal that these cells are important in driving recovery sleep to regain sleep homeostasis. We concluded that these cells are not critical for normal sleep-wake state regulation, since 1) activating these cells promotes sleep irrespective of low sleep, and 2) there is no effect of inhibiting these cells when normal sleep-wake patterns occur. In conclusion, we successfully identified and characterized a new cellular population involved in sleep homeostasis.

We also identified that a population of non-neuronal cells called astrocytes in the brain’s cortex that are sensitive to changes in sleep pressure. With sleep loss, we found altered protein expression in these cells. Furthermore, we found that activation of these astrocytes in the cortex promoted sleep onset, but only after sleep deprivation. In conclusion, we gained significant understanding of the role of astrocytes in sleep homeostasis.

Theses results have bene presented in part at international conferences. The resulting manuscripts which report these scientific advances are in preparation. As there is no current funding to cover publication submission fees, we aim to deposit these results in an online archive for dissemination to the research community.

Innowacyjność oraz oczekiwany potencjalny wpływ (w tym dotychczasowe znaczenie społeczno-gospodarcze i szersze implikacje społeczne projektu)

We created an unprecedented brain-wide map of cellular activity under conditions of sleep deprivation and recovery sleep, leading to the identification of a previously unknown population of cells activated by sleep deprivation in the amygdala. For the first time, we were able to gain specific pharmacological access to these cells to switch them on and off and observe the effects on sleep, leading to understanding of their role in sleep regulation. Finally, for the first time, we demonstrated changes in the shape of astrocytes, as marked by the expression of a protein, with sleep deprivation.

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