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関連する概念動画

Synaptic Signaling01:12

Synaptic Signaling

Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
Synaptic Signaling01:09

Synaptic Signaling

Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
Most synapses are chemical, meaning an electrical impulse or action potential spurs the release of chemical messengers called neurotransmitters. The neuron sending the signal is called the presynaptic neuron, and the neuron receiving the signal is the postsynaptic neuron.
The presynaptic neuron fires an action potential that...
Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Laminins are the Adhesive Proteins of Basal Lamina00:55

Laminins are the Adhesive Proteins of Basal Lamina

Laminins are heterotrimeric proteins with high molecular mass found in the extracellular matrix. Each laminin molecule is composed of three chains, viz. alpha, beta, and gamma, coded by five, four, and three paralogous genes, respectively. Laminins are categories based on the compositions of the three chains.
In humans, the five forms of alpha chains are LAMA 1, LAMA 2, LAMA 3, LAMA 4, and LAMA 5. The four forms of beta chains are LAMB 1, LAMB 2, LAMB 3, and LAMB 4. The three forms of gamma...
Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...

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関連する実験動画

Updated: Jul 27, 2026

Preparation of Synaptic Plasma Membrane and Postsynaptic Density Proteins Using a Discontinuous Sucrose Gradient
08:06

Preparation of Synaptic Plasma Membrane and Postsynaptic Density Proteins Using a Discontinuous Sucrose Gradient

Published on: September 3, 2014

シナプスラミニンは,シナプス裂け目への膠質の侵入を防ぐ.

B L Patton1, A Y Chiu, J R Sanes

  • 1Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, Missouri 63110, USA.

Nature
|June 26, 1998
PubMed
まとめ

シュヴァン細胞は,膠質細胞の一種であり,シナプス裂け目に侵入することを積極的に防ぐ. シナプス裂けのラミニン11は,この膠質細胞の侵入を抑制し,神経筋シナプスの安定性を維持します.

科学分野:

  • 神経科学は神経科学である.
  • 細胞生物学 細胞生物学
  • シナプスの可塑性

背景:

  • 化学的シナプスは,迅速な情報伝達のために,シナプス前とシナプス後の膜の直接的な対立を必要とします.
  • 超シナプスニューロン表面は,シナプス裂け目とは異なり,通常は膠質細胞で覆われています.
  • シナプスの安定性は,シナプスの要素間の緊密な結合に依存すると考えられています.

研究 の 目的:

  • 骨格神経筋シナプスのシナプス安定を維持するメカニズムを調査する.
  • 膠質細胞 (シュワンン細胞) がシナプス裂け目に侵入するのを防ぐ要因を特定する.
  • シナプス維持と可塑性におけるグリアル-ニューロン相互作用の役割を理解する.

主な方法:

  • シュワン細胞と,骨格神経筋肉の交差点にあるシナプス裂け目の相互作用を研究した.
  • シナプス裂け目内の分子成分を特定し,膠質細胞の行動を調節する.
  • ラミニン11がシナプス裂け目のシュワンン細胞侵入を抑制する役割を調べました.

主要な成果:

  • シュワン細胞,神経筋シナプスの膠質細胞は,シナプス裂け目に侵入することを積極的に阻害されます.
  • ラミニン11は,シナプス裂け目に濃縮されたグリコタンパク質で,抑制成分として作用します.

さらに関連する動画

Inhibitory Synapse Formation in a Co-culture Model Incorporating GABAergic Medium Spiny Neurons and HEK293 Cells Stably Expressing GABAA Receptors
07:51

Inhibitory Synapse Formation in a Co-culture Model Incorporating GABAergic Medium Spiny Neurons and HEK293 Cells Stably Expressing GABAA Receptors

Published on: November 14, 2014

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo
10:50

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo

Published on: March 26, 2019

関連する実験動画

Last Updated: Jul 27, 2026

Preparation of Synaptic Plasma Membrane and Postsynaptic Density Proteins Using a Discontinuous Sucrose Gradient
08:06

Preparation of Synaptic Plasma Membrane and Postsynaptic Density Proteins Using a Discontinuous Sucrose Gradient

Published on: September 3, 2014

Inhibitory Synapse Formation in a Co-culture Model Incorporating GABAergic Medium Spiny Neurons and HEK293 Cells Stably Expressing GABAA Receptors
07:51

Inhibitory Synapse Formation in a Co-culture Model Incorporating GABAergic Medium Spiny Neurons and HEK293 Cells Stably Expressing GABAA Receptors

Published on: November 14, 2014

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo
10:50

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo

Published on: March 26, 2019

  • この抑制は,神経筋シナプスの構造と安定性を維持するために不可欠です.
  • 結論:

    • シナプス裂け目からのグリアル細胞の排除は,活発に調節され,シナプス維持に不可欠です.
    • ラミニン11は,シュワンの細胞がシナプス裂け目に侵入するのを抑制する上で重要な役割を果たします.
    • この膠質ニューロン阻害相互作用の調節障害は,特にシナプス後の損傷後に,シナプス不安定性と損失につながる可能性があります.