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Live-cell imaging of neurofilament transport in cultured neurons.
Uchida, Atsuko; Monsma, Paula C; Fenn, J Daniel; Brown, Anthony.
Afiliação
  • Uchida A; Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
  • Monsma PC; Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
  • Fenn JD; Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
  • Brown A; Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
Methods Cell Biol ; 131: 21-90, 2016.
Article em En | MEDLINE | ID: mdl-26794508
Neurofilaments, which are the intermediate filaments of nerve cells, are space-filling cytoskeletal polymers that contribute to the growth of axonal caliber. In addition to their structural role, neurofilaments are cargos of axonal transport that move along microtubule tracks in a rapid, intermittent, and bidirectional manner. Though they measure just 10nm in diameter, which is well below the diffraction limit of optical microscopes, these polymers can reach 100 µm or more in length and are often packed densely, just tens of nanometers apart. These properties of neurofilaments present unique challenges for studies on their movement. In this article, we describe several live-cell fluorescence imaging strategies that we have developed to image neurofilament transport in axons of cultured neurons on short and long timescales. Together, these methods form a powerful set of complementary tools with which to study the axonal transport of these unique intracellular cargos.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Axônios / Transporte Axonal / Filamentos Intermediários / Microtúbulos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Axônios / Transporte Axonal / Filamentos Intermediários / Microtúbulos Idioma: En Ano de publicação: 2016 Tipo de documento: Article