Postsynaptic density

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Postsynaptic density


Postsynaptic density (PSD) is a specialized area of the neuron that is located at the postsynaptic terminal of a synapse. It is a dense complex of proteins that is organized into a network and is responsible for the reception and processing of neurotransmitter signals.

Structure[edit | edit source]

The PSD is a disc-shaped structure, approximately 30-40 nanometers thick and 300-400 nanometers in diameter. It is composed of a variety of proteins, including receptor proteins, ion channels, and signaling proteins. The PSD is anchored to the postsynaptic membrane and is in close proximity to the presynaptic terminal, allowing for efficient signal transmission.

Function[edit | edit source]

The primary function of the PSD is to receive and process signals from the presynaptic neuron. This is achieved through the action of receptor proteins and ion channels, which bind to neurotransmitters and initiate a cascade of intracellular events. The PSD also plays a crucial role in synaptic plasticity, the ability of synapses to strengthen or weaken over time. This is thought to be a key mechanism underlying learning and memory.

Composition[edit | edit source]

The PSD is composed of a large number of proteins, with estimates ranging from several hundred to over a thousand. These proteins can be broadly categorized into three groups:

1. Receptor proteins: These proteins bind to neurotransmitters released from the presynaptic neuron. The most common types of receptor proteins in the PSD are glutamate receptors, including NMDA receptors and AMPA receptors.

2. Ion channels: These proteins allow for the flow of ions across the postsynaptic membrane, leading to changes in the postsynaptic neuron's electrical potential.

3. Signaling proteins: These proteins are involved in the intracellular signaling pathways that are activated by receptor proteins and ion channels. They include kinases, phosphatases, and GTPases.

Clinical significance[edit | edit source]

Alterations in the structure or function of the PSD have been implicated in a number of neurological and psychiatric disorders, including schizophrenia, autism, and Alzheimer's disease. Research in this area is ongoing and may lead to the development of new therapeutic strategies.

See also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD