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Electrical synaptic transmission requires a postsynaptic scaffolding protein.
Lasseigne, Abagael M; Echeverry, Fabio A; Ijaz, Sundas; Michel, Jennifer Carlisle; Martin, E Anne; Marsh, Audrey J; Trujillo, Elisa; Marsden, Kurt C; Pereda, Alberto E; Miller, Adam C.
Afiliação
  • Lasseigne AM; Institute of Neuroscience, University of Oregon, Eugene, United States.
  • Echeverry FA; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, United States.
  • Ijaz S; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, United States.
  • Michel JC; Institute of Neuroscience, University of Oregon, Eugene, United States.
  • Martin EA; Institute of Neuroscience, University of Oregon, Eugene, United States.
  • Marsh AJ; Institute of Neuroscience, University of Oregon, Eugene, United States.
  • Trujillo E; Institute of Neuroscience, University of Oregon, Eugene, United States.
  • Marsden KC; Department of Biological Sciences, NC State University, Raleigh, United States.
  • Pereda AE; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, United States.
  • Miller AC; Institute of Neuroscience, University of Oregon, Eugene, United States.
Elife ; 102021 04 28.
Article em En | MEDLINE | ID: mdl-33908867
Neurons 'talk' with each another at junctions called synapses, which can either be chemical or electrical. Communication across a chemical synapse involves a 'sending' neuron releasing chemicals that diffuse between the cells and subsequently bind to specialized receptors on the receiving neuron. These complex junctions involve a large number of well-studied molecular actors. Electrical synapses, on the other hand, are believed to be simpler. There, neurons are physically connected via channels formed of 'connexin' proteins, which allow electrically charged ions to flow between the cells. However, it is likely that other proteins help to create these structures. In particular, recent evidence shows that without a structurally supporting 'scaffolding' protein called ZO1, electrical synapses cannot form in the brain of a tiny freshwater fish known as zebrafish. As their name implies, scaffolding proteins help cells organize their internal structure, for example by anchoring other molecules to the cell membrane. By studying electrical synapses in zebrafish, Lasseigne, Echeverry, Ijaz, Michel et al. now show that these structures are more complex than previously assumed. In particular, the experiments reveal that ZO1 proteins are only present on one side of electrical synapses; despite their deceptively symmetrical anatomical organization, these junctions can be asymmetric, like their chemical cousins. The results also show that ZO1 must be present for connexins to gather at electrical synapses, whereas the converse is not true. This suggests that when a new electrical synapse forms, ZO1 moves into position first: it then recruits or stabilizes connexins to form the channels connecting the two cells. In many animals with a spine, electrical synapses account for about 20% of all neural junctions. Understanding how these structures form and work could help to find new treatments for disorders linked to impaired electrical synapses, such as epilepsy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article