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Whole-brain calcium imaging with cellular resolution in freely behaving Caenorhabditis elegans.
Nguyen, Jeffrey P; Shipley, Frederick B; Linder, Ashley N; Plummer, George S; Liu, Mochi; Setru, Sagar U; Shaevitz, Joshua W; Leifer, Andrew M.
Afiliación
  • Nguyen JP; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544; Department of Physics, Princeton University, Princeton, NJ 08544;
  • Shipley FB; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544;
  • Linder AN; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544.
  • Plummer GS; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544;
  • Liu M; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544;
  • Setru SU; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544;
  • Shaevitz JW; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544; Department of Physics, Princeton University, Princeton, NJ 08544;
  • Leifer AM; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544; leifer@princeton.edu.
Proc Natl Acad Sci U S A ; 113(8): E1074-81, 2016 Feb 23.
Article en En | MEDLINE | ID: mdl-26712014
ABSTRACT
The ability to acquire large-scale recordings of neuronal activity in awake and unrestrained animals is needed to provide new insights into how populations of neurons generate animal behavior. We present an instrument capable of recording intracellular calcium transients from the majority of neurons in the head of a freely behaving Caenorhabditis elegans with cellular resolution while simultaneously recording the animal's position, posture, and locomotion. This instrument provides whole-brain imaging with cellular resolution in an unrestrained and behaving animal. We use spinning-disk confocal microscopy to capture 3D volumetric fluorescent images of neurons expressing the calcium indicator GCaMP6s at 6 head-volumes/s. A suite of three cameras monitor neuronal fluorescence and the animal's position and orientation. Custom software tracks the 3D position of the animal's head in real time and two feedback loops adjust a motorized stage and objective to keep the animal's head within the field of view as the animal roams freely. We observe calcium transients from up to 77 neurons for over 4 min and correlate this activity with the animal's behavior. We characterize noise in the system due to animal motion and show that, across worms, multiple neurons show significant correlations with modes of behavior corresponding to forward, backward, and turning locomotion.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Conducta Animal / Calcio / Caenorhabditis elegans / Imagen Molecular / Neuronas Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Conducta Animal / Calcio / Caenorhabditis elegans / Imagen Molecular / Neuronas Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article