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Complexity of dendritic SER increases at enlarging synapses during LTP

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-9861(20000306)418:2<164::aid-cne4>3.0.co;2-0openalex-snapshot

Actin-associated protein synaptopodin in the rat hippocampal formation: Localization in the spine neck and close association with the spine apparatus of principal neurons

inferredcites →https://doi.org/10.1002/cne.10825openalex-snapshot

Timing of neuronal and glial ultrastructure disruption during brain slice preparation and recovery in vitro

inferredcites →https://doi.org/10.1002/hipo.20238openalex-snapshot

Polyribosomes are increased in spines of CA1 dendrites 2 h after the induction of LTP in mature rat hippocampal slices

inferredcites →https://doi.org/10.1002/hipo.20768openalex-snapshot

Coordination of size and number of excitatory and inhibitory synapses results in a balanced structural plasticity along mature hippocampal CA1 dendrites during LTP

inferredcites →https://doi.org/10.1016/0006-8993(83)91322-7openalex-snapshot

Calcium in the spine apparatus of dendritic spines in the dentate molecular layer

inferredcites →https://doi.org/10.1016/0006-8993(91)91683-ropenalex-snapshot

Induction of long-term potentiation is associated with an increase in the number of axospinous synapses with segmented postsynaptic densities

inferredcites →https://doi.org/10.1016/0166-2236(95)93919-oopenalex-snapshot

Neuronal Ca2+ stores: activation and function

inferredcites →https://doi.org/10.1016/0896-6273(95)90046-2openalex-snapshot

Evidence for silent synapses: Implications for the expression of LTP

inferredcites →https://doi.org/10.1016/j.cell.2011.11.056openalex-snapshot

Local Zones of Endoplasmic Reticulum Complexity Confine Cargo in Neuronal Dendrites

inferredcites →https://doi.org/10.1016/j.conb.2011.09.002openalex-snapshot

Structural plasticity of dendritic spines

inferredcites →https://doi.org/10.1016/j.neuron.2005.11.005openalex-snapshot

Polarized Secretory Trafficking Directs Cargo for Asymmetric Dendrite Growth and Morphogenesis

inferredcites →https://doi.org/10.1016/j.neuron.2006.09.040openalex-snapshot

Plasticity-Induced Growth of Dendritic Spines by Exocytic Trafficking from Recycling Endosomes

inferredcites →https://doi.org/10.1016/j.neuron.2008.08.020openalex-snapshot

Calcium Signaling in Dendrites and Spines: Practical and Functional Considerations

inferredcites →https://doi.org/10.1016/j.neuron.2014.02.031openalex-snapshot

Balance and Stability of Synaptic Structures during Synaptic Plasticity

inferredcites →https://doi.org/10.1016/j.neuropharm.2006.07.009openalex-snapshot

Priming of long-term potentiation mediated by ryanodine receptor activation in rat hippocampal slices

inferredcites →https://doi.org/10.1016/s0143-4160(96)90009-3openalex-snapshot

Calcium-induced calcium release in neurones

inferredcites →https://doi.org/10.1016/s0166-2236(00)01891-9openalex-snapshot

Structural complexity and functional diversity of endoplasmic reticulum Ca2+ stores

inferredcites →https://doi.org/10.1016/s0306-4522(02)00803-5openalex-snapshot

Long-term potentiation and long-term depression in hippocampal CA1 neurons of mice lacking the IP3 type 1 receptor

inferredcites →https://doi.org/10.1016/s0896-6273(00)80510-3openalex-snapshot

Neuronal Calcium Signaling

inferredcites →https://doi.org/10.1016/s0896-6273(00)80683-2openalex-snapshot

Single Synaptic Events Evoke NMDA Receptor–Mediated Release of Calcium from Internal Stores in Hippocampal Dendritic Spines

inferredcites →https://doi.org/10.1016/s0896-6273(01)00402-0openalex-snapshot

Stores Not Just for Storage

inferredcites →https://doi.org/10.1016/s0896-6273(02)00785-7openalex-snapshot

Polyribosomes Redistribute from Dendritic Shafts into Spines with Enlarged Synapses during LTP in Developing Rat Hippocampal Slices

inferredcites →https://doi.org/10.1016/s0960-9822(01)00077-xopenalex-snapshot

Evidence for a satellite secretory pathway in neuronal dendritic spines

inferredcites →https://doi.org/10.1038/35046067openalex-snapshot

Calcium stores regulate the polarity and input specificity of synaptic modification

inferredcites →https://doi.org/10.1038/nature07842openalex-snapshot

Activation of CaMKII in single dendritic spines during long-term potentiation

inferredcites →https://doi.org/10.1038/nrn3531openalex-snapshot

Nuclear calcium signalling in the regulation of brain function

inferredcites →https://doi.org/10.1042/bst20130081openalex-snapshot

Dendritic trafficking for neuronal growth and plasticity

inferredcites →https://doi.org/10.1073/pnas.0905110106openalex-snapshot

Differential distribution of endoplasmic reticulum controls metabotropic signaling and plasticity at hippocampal synapses

inferredcites →https://doi.org/10.1073/pnas.1832384100openalex-snapshot

Synaptopodin-deficient mice lack a spine apparatus and show deficits in synaptic plasticity

inferredcites →https://doi.org/10.1073/pnas.86.23.9574openalex-snapshot

A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory.

inferredcites →https://doi.org/10.1091/mbc.e04-07-0554openalex-snapshot

Phosphorylation Controls CLIMP-63–mediated Anchoring of the Endoplasmic Reticulum to Microtubules

inferredcites →https://doi.org/10.1093/emboj/17.21.6168openalex-snapshot

A novel direct interaction of endoplasmic reticulum with microtubules

inferredcites →https://doi.org/10.1101/lm.1255909openalex-snapshot

Priming of short-term potentiation and synaptic tagging/capture mechanisms by ryanodine receptor activation in rat hippocampal CA1

inferredcites →https://doi.org/10.1111/j.1460-9568.2005.03999.xopenalex-snapshot

Translation of an integral membrane protein in distal dendrites of hippocampal neurons

inferredcites →https://doi.org/10.1113/jphysiol.2005.098947openalex-snapshot

Spatial segregation of neuronal calcium signals encodes different forms of LTP in rat hippocampus

inferredcites →https://doi.org/10.1113/jphysiol.2009.168930openalex-snapshot

Inositol‐1,4,5‐trisphosphate receptor‐mediated Ca2+ waves in pyramidal neuron dendrites propagate through hot spots and cold spots

inferredcites →https://doi.org/10.1126/science.1102026openalex-snapshot

Recycling Endosomes Supply AMPA Receptors for LTP

inferredcites →https://doi.org/10.1126/science.1159675openalex-snapshot

The Spread of Ras Activity Triggered by Activation of a Single Dendritic Spine

inferredcites →https://doi.org/10.1126/science.2549638openalex-snapshot

Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP

inferredcites →https://doi.org/10.1126/science.8394601openalex-snapshot

An Essential Role for Protein Phosphatases in Hippocampal Long-Term Depression

inferredcites →https://doi.org/10.1146/annurev.neuro.24.1.1071openalex-snapshot

Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity

inferredcites →https://doi.org/10.1152/jn.2002.88.1.249openalex-snapshot

Different Calcium Sources Are Narrowly Tuned to the Induction of Different Forms of LTP

inferredcites →https://doi.org/10.1523/jneurosci.0381-14.2014openalex-snapshot

Synaptopodin Regulates Spine Plasticity: Mediation by Calcium Stores

inferredcites →https://doi.org/10.1523/jneurosci.13-07-03051.1993openalex-snapshot

Differential immunohistochemical localization of inositol 1,4,5- trisphosphate- and ryanodine-sensitive Ca2+ release channels in rat brain

inferredcites →https://doi.org/10.1523/jneurosci.17-01-00190.1997openalex-snapshot

Three-Dimensional Organization of Smooth Endoplasmic Reticulum in Hippocampal CA1 Dendrites and Dendritic Spines of the Immature and Mature Rat

inferredcites →https://doi.org/10.1523/jneurosci.19-01-00168.1999openalex-snapshot

Dendritic and Postsynaptic Protein Synthetic Machinery

inferredcites →https://doi.org/10.1523/jneurosci.22-06-02215.2002openalex-snapshot

Endosomal Compartments Serve Multiple Hippocampal Dendritic Spines from a Widespread Rather Than a Local Store of Recycling Membrane

inferredcites →https://doi.org/10.1523/jneurosci.4822-04.2005openalex-snapshot

Key Role of the Postsynaptic Density Scaffold Proteins Shank and Homer in the Functional Architecture of Ca 2+ Homeostasis at Dendritic Spines in Hippocampal Neurons

inferredcites →https://doi.org/10.1523/jneurosci.5528-08.2009openalex-snapshot

Synaptopodin Regulates Plasticity of Dendritic Spines in Hippocampal Neurons

inferredcites →https://doi.org/10.3389/fnana.2014.00064openalex-snapshot

Endoplasmic reticulum calcium stores in dendritic spines

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.nlm.2016.07.023openalex-snapshot

Understanding the role of synaptopodin and the spine apparatus in Hebbian synaptic plasticity – New perspectives and the need for computational modeling

inferred← citeshttps://doi.org/10.1038/s41598-018-38412-7openalex-snapshot

Neuronal plasticity affects correlation between the size of dendritic spine and its postsynaptic density

inferred← citeshttps://doi.org/10.1113/jp277726openalex-snapshot

Intracellular calcium stores mediate metaplasticity at hippocampal dendritic spines

inferred← citeshttps://doi.org/10.70675/275d3182za2b9z4513z9941z62d044306e33openalex-snapshot

Rôle du microARN miR-124 dans la plasticité homéostatique via le contrôle de l’expression de la synaptopodine et des récepteurs AMPA dans les neurones de l'hippocampe

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