Your browser doesn't support javascript.
loading
Versatile live-cell activity analysis platform for characterization of neuronal dynamics at single-cell and network level.
Yuan, Xinyue; Schröter, Manuel; Obien, Marie Engelene J; Fiscella, Michele; Gong, Wei; Kikuchi, Tetsuhiro; Odawara, Aoi; Noji, Shuhei; Suzuki, Ikuro; Takahashi, Jun; Hierlemann, Andreas; Frey, Urs.
Afiliação
  • Yuan X; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland. xinyue.yuan@bsse.ethz.ch.
  • Schröter M; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
  • Obien MEJ; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
  • Fiscella M; MaxWell Biosystems AG, Zurich, Switzerland.
  • Gong W; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
  • Kikuchi T; MaxWell Biosystems AG, Zurich, Switzerland.
  • Odawara A; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
  • Noji S; MaxWell Biosystems AG, Zurich, Switzerland.
  • Suzuki I; Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
  • Takahashi J; Tohoku Institute of Technology, Sendai, Japan.
  • Hierlemann A; Tohoku Institute of Technology, Sendai, Japan.
  • Frey U; Tohoku Institute of Technology, Sendai, Japan.
Nat Commun ; 11(1): 4854, 2020 09 25.
Article em En | MEDLINE | ID: mdl-32978383
ABSTRACT
Chronic imaging of neuronal networks in vitro has provided fundamental insights into mechanisms underlying neuronal function. Current labeling and optical imaging methods, however, cannot be used for continuous and long-term recordings of the dynamics and evolution of neuronal networks, as fluorescent indicators can cause phototoxicity. Here, we introduce a versatile platform for label-free, comprehensive and detailed electrophysiological live-cell imaging of various neurogenic cells and tissues over extended time scales. We report on a dual-mode high-density microelectrode array, which can simultaneously record in (i) full-frame mode with 19,584 recording sites and (ii) high-signal-to-noise mode with 246 channels. We set out to demonstrate the capabilities of this platform with recordings from primary and iPSC-derived neuronal cultures and tissue preparations over several weeks, providing detailed morpho-electrical phenotypic parameters at subcellular, cellular and network level. Moreover, we develop reliable analysis tools, which drastically increase the throughput to infer axonal morphology and conduction speed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Célula Única / Imagem Óptica / Rede Nervosa / Neurônios Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Célula Única / Imagem Óptica / Rede Nervosa / Neurônios Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça