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Related Concept Videos

Physiological Barriers01:25

Physiological Barriers

Physiological barriers are semi-permeable cellular structures restricting drug diffusion into intracellular compartments and tissues. There are six types of physiological barriers: blood endothelial, cell membrane, blood-brain, blood-cerebrospinal fluid (CSF), blood-placenta, and blood-testis barriers.
The blood endothelial barrier is the most porous of these. It allows all small ionized, un-ionized, and lipophilic molecules to pass through the endothelial lining into the interstitial space...
Factors Affecting Drug Distribution: Physiological Barriers01:23

Factors Affecting Drug Distribution: Physiological Barriers

Drug distribution in the body is intricately regulated by various physiological barriers that control the passage of substances. These include the capillary endothelial barrier, the blood-brain, blood-cerebrospinal fluid, blood-placental, and blood-testis barriers.
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The...
Protein Diffusion in the Membrane01:24

Protein Diffusion in the Membrane

Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...
The Blood-brain Barrier00:49

The Blood-brain Barrier

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Facilitated Diffusion01:16

Facilitated Diffusion

The plasma membrane, a critical structure in cellular biology, houses an array of transporters, or carrier proteins, interspersed within its lipid bilayer. These proteins play a crucial role in solute transport through facilitated diffusion, a form of passive diffusion that uses transporters to move the molecules across the membrane.
In this process, substrates such as organic compounds and ions interact with a transporter on one side, triggering conformational changes in proteins that enable...
Cellular Membranes and Drug Transport01:24

Cellular Membranes and Drug Transport

Drugs must traverse multiple biological barriers, such as multi-layered skin, single-layered intestinal epithelium, and the plasma membrane, to reach their target sites within the body. The plasma membrane, a highly structured composite of phospholipids, carbohydrates, and proteins, is the cell's protective boundary, facilitating selective substance exchange.
Phospholipids arrange themselves into a bilayer, with hydrophilic heads oriented outward and hydrophobic tails facing inward.

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Related Experiment Video

Updated: May 19, 2026

Models and Methods to Evaluate Transport of Drug Delivery Systems Across Cellular Barriers
18:57

Models and Methods to Evaluate Transport of Drug Delivery Systems Across Cellular Barriers

Published on: October 17, 2013

Diffusion barriers constrain receptors at synapses.

Marianne Renner1, Claude Schweizer, Hiroko Bannai

  • 1Institut de Biologie de l'Ecole Normale Supérieure, Institut National de la Santé et de la Recherche Médicale U1024, Centre National de la Recherche Scientifique UMR8197, Paris, France.

Plos One
|August 23, 2012
PubMed
Summary
This summary is machine-generated.

Neurotransmitter receptor movement in synapses is restricted by cellular barriers. Receptor confinement and dwell time, not diffusion speed, dictate synaptic sorting and accumulation.

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Published on: February 29, 2012

Area of Science:

  • Neuroscience
  • Cell Biology
  • Biophysics

Background:

  • Synaptic function relies on neurotransmitter receptor trafficking.
  • Transmembrane proteins and cytoskeletal elements can impede receptor diffusion within synapses.

Purpose of the Study:

  • To investigate the membrane diffusion and synaptic residency of GABA(A) receptor subunits.
  • To explore how synaptic barriers and scaffold interactions influence receptor dynamics.

Main Methods:

  • Studied membrane diffusion of GABA(A) receptor subunits (γ2 and α5) in rat hippocampal neurons using single-particle tracking.
  • Utilized a gephyrin dominant-negative approach to assess scaffold interactions.
  • Examined the diffusion of AMPA receptor subunit GluA2.

Main Results:

  • Both clustered (γ2) and non-clustered (α5) GABA(A)R subunits showed reduced diffusion and increased confinement at synapses.
  • γ2 receptors exhibited greater confinement and longer dwell times at inhibitory synapses compared to α5, suggesting faster α5 synaptic escape.
  • Receptor-scaffold interactions, specifically with gephyrin, were crucial for γ2 receptor retention at inhibitory synapses.
  • Excitatory AMPA receptor subunit GluA2 also displayed restricted mobility and differential residency at synapses.

Conclusions:

  • Synaptic barriers significantly constrain receptor diffusion.
  • Confinement and dwell time, rather than diffusion coefficient alone, are key indicators of synapse-specific receptor sorting, trapping, and accumulation.
  • Receptor-scaffold interactions play a critical role in regulating receptor dynamics at inhibitory synapses.