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  Skewed distribution of spines is independent of presynaptic transmitter release and synaptic plasticity, and emerges early during adult neurogenesis

Rößler, N., Jungenitz, T., Sigler, A., Bird, A., Mittag, M., Rhee, J. S., et al. (2023). Skewed distribution of spines is independent of presynaptic transmitter release and synaptic plasticity, and emerges early during adult neurogenesis. Open Biology, 13(8): 230063. doi:10.1098/rsob.230063.

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Rößler, Nina, Author
Jungenitz, Tassilo, Author
Sigler, Albrecht1, Author           
Bird, Alexander, Author
Mittag, Martin, Author
Rhee, Jeong Seop1, Author           
Deller, Thomas, Author
Cuntz, Hermann, Author
Brose, Nils1, Author           
Schwarzacher, Stephan W., Author
Jedlicka, Peter, Author
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1Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society, ou_3350300              

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 Abstract: Dendritic spines are crucial for excitatory synaptic transmission as the size of a spine head correlates with the strength of its synapse. The distribution of spine head sizes follows a lognormal-like distribution with more small spines than large ones. We analysed the impact of synaptic activity and plasticity on the spine size distribution in adult-born hippocampal granule cells from rats with induced homo- and heterosynaptic long-term plasticity in vivo and CA1 pyramidal cells from Munc13–1/Munc13–2 knockout mice with completely blocked synaptic transmission. Neither the induction of extrinsic synaptic plasticity nor the blockage of presynaptic activity degrades the lognormal-like distribution but changes its mean, variance and skewness. The skewed distribution develops early in the life of the neuron. Our findings and their computational modelling support the idea that intrinsic synaptic plasticity is sufficient for the generation, while a combination of intrinsic and extrinsic synaptic plasticity maintains lognormal-like distribution of spines.

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Language(s): eng - English
 Dates: 2023-08-02
 Publication Status: Published online
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 Rev. Type: Peer
 Identifiers: DOI: 10.1098/rsob.230063
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Project name : This research was supported by the German Research Foundation (Deutsche Forschungsgemeinschaft), grant nos. 467764793, JE 528/10–1 (to P.J.), CRC1080 (to T.D.) and SCHW 534/6–1 (to S.W.S.), by the Kogge-Stiftung (to P.J.), by funds from the von Behring Röntgen Foundation (to P.J.) and DFG German Israeli Project Cooperation (ZI 1039/1-1 | RU 900/5-1 to N.B.).
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Title: Open Biology
Source Genre: Journal
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Publ. Info: London : The Royal Society
Pages: - Volume / Issue: 13 (8) Sequence Number: 230063 Start / End Page: - Identifier: ISSN: 2046-2441
CoNE: https://pure.mpg.de/cone/journals/resource/2046-2441