Computation, wiring, and plasticity in synaptic clusters. (October 2021)
- Record Type:
- Journal Article
- Title:
- Computation, wiring, and plasticity in synaptic clusters. (October 2021)
- Main Title:
- Computation, wiring, and plasticity in synaptic clusters
- Authors:
- Pulikkottil, Vinu Varghese
Somashekar, Bhanu Priya
Bhalla, Upinder S. - Abstract:
- Abstract: Synaptic clusters on dendrites are extraordinarily compact computational building blocks. They contribute to key local computations through biophysical and biochemical signaling that utilizes convergence in space and time as an organizing principle. However, these computations can only arise in very special contexts. Dendritic cluster computations, their highly organized input connectivity, and the mechanisms for their formation are closely linked, yet these have not been analyzed as parts of a single process. Here, we examine these linkages. The sheer density of axonal and dendritic arborizations means that there are far more potential connections (close enough for a spine to reach an axon) than actual ones. We see how dendritic clusters draw upon electrical, chemical, and mechano–chemical signaling to implement the rules for formation of connections and subsequent computations. Crucially, the same mechanisms that underlie their functions also underlie their formation. Graphical abstract: Image 1 Highlights: Clustered synaptic inputs subserve key dendritic computations including correlation detection and sequence discrimination. Multiple kinds of spatial signaling, including electrical, chemical and mechano-chemical, underlie these computations. Clustered computation requires convergent input with temporally organized activity. Mechano-chemical signaling and spatio-temporal learning rules select for inputs relevant to dendritic computation. The processes thatAbstract: Synaptic clusters on dendrites are extraordinarily compact computational building blocks. They contribute to key local computations through biophysical and biochemical signaling that utilizes convergence in space and time as an organizing principle. However, these computations can only arise in very special contexts. Dendritic cluster computations, their highly organized input connectivity, and the mechanisms for their formation are closely linked, yet these have not been analyzed as parts of a single process. Here, we examine these linkages. The sheer density of axonal and dendritic arborizations means that there are far more potential connections (close enough for a spine to reach an axon) than actual ones. We see how dendritic clusters draw upon electrical, chemical, and mechano–chemical signaling to implement the rules for formation of connections and subsequent computations. Crucially, the same mechanisms that underlie their functions also underlie their formation. Graphical abstract: Image 1 Highlights: Clustered synaptic inputs subserve key dendritic computations including correlation detection and sequence discrimination. Multiple kinds of spatial signaling, including electrical, chemical and mechano-chemical, underlie these computations. Clustered computation requires convergent input with temporally organized activity. Mechano-chemical signaling and spatio-temporal learning rules select for inputs relevant to dendritic computation. The processes that govern cluster computation and cluster formation have much in common. … (more)
- Is Part Of:
- Current opinion in neurobiology. Volume 70(2021)
- Journal:
- Current opinion in neurobiology
- Issue:
- Volume 70(2021)
- Issue Display:
- Volume 70, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 70
- Issue:
- 2021
- Issue Sort Value:
- 2021-0070-2021-0000
- Page Start:
- 101
- Page End:
- 112
- Publication Date:
- 2021-10
- Subjects:
- bAPs Back-propagating action potentials -- BDNF Brain-derived neurotrophic factor -- cAMP Cyclic adenosine monophosphate -- Cdc42 Cell division control protein 42 homolog -- CICR Calcium-induced calcium release -- dLTP Dendritic spike-dependent long-term potentiation -- I-BAR inverse-Bin-Amphiphysin-Rvs -- IRSp53 Insulin Receptor Substrate protein 53 kDa -- LTD Long-term depression -- LTP Long-term potentiation -- mGluR Metabotropic glutamate receptor -- MIM Missing-In-Metastasis -- MMP9 Matrix metalloproteinase-9 -- MAPK Mitogen-activated protein kinase -- NMDAR N-methyl-d-aspartate receptor -- PLC Phospholipase C -- PRPs Plasticity-related proteins -- STDP Spike-timing dependent plasticity -- SER Smooth endoplasmic reticulum -- TRPV4 Transient receptor potential cation channel subfamily V member 4 -- VGCC Voltage-gated calcium channel
Neurobiology -- Periodicals
573.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09594388/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.conb.2021.08.001 ↗
- Languages:
- English
- ISSNs:
- 0959-4388
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.775850
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20273.xml