Gap junction: Difference between revisions
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File:Gap_cell_junction-en.svg|Gap junction | |||
File:Camillo_Peracchia_fig4-6.png|Camillo Peracchia's figure | |||
File:Validation_of_the_dye_diffusion_assay_performed_with_the_flattened_cochlear_preparation.png|Validation of the dye diffusion assay | |||
File:Cell_pannexin_tree.svg|Cell pannexin tree | |||
File:Perinexial_ephaptic_coupling.jpg|Perinexial ephaptic coupling | |||
File:Lens3Dmap_with_txt.jpg|Lens 3D map | |||
File:Epithelium_Cx50.jpg|Epithelium Cx50 | |||
File:Fiber_ends_Cx50-1.jpg|Fiber ends Cx50 | |||
File:Connexin43-Modulates-Cell-Polarity-and-Directional-Cell-Migration-by-Regulating-Microtubule-Dynamics-pone.0026379.s004.ogv|Connexin43 modulates cell polarity | |||
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Revision as of 12:23, 18 February 2025
Gap junctions are specialized intercellular connections between a multitude of animal cell-types. They directly connect the cytoplasm of two cells, which allows various molecules, ions and electrical impulses to directly pass through a regulated gate between cells.
Structure
One gap junction channel is composed of two connexons (or hemichannels), which connect across the intercellular space. Gap junctions are analogous to the plasmodesmata that join plant cells.
Function
Gap junctions occur in virtually all tissues of the body, with the exception of adult fully developed skeletal muscle and mobile cell types such as sperm or erythrocytes. They are not found in simpler organisms such as sponges and slime molds.
Clinical significance
Mutations in gap junction proteins, called connexins, can lead to a variety of human diseases, including erythrokeratodermia variabilis, hearing loss, skin disease, cataracts, and cardiac disease.
See also
References
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