English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  On-demand optogenetic activation of human stem-cell-derived neurons

Klapper, S. D., Sauter, E. J., Swiersy, A., Hyman, M. A., Bamann, C., Bamberg, E., et al. (2017). On-demand optogenetic activation of human stem-cell-derived neurons. Scientific Reports, 7: 14450. doi:doi:10.1038/s41598-017-14827-6.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Klapper, Simon D.1, Author
Sauter, Evelyn J.1, Author
Swiersy, Anka1, Author
Hyman, Max A.E.1, Author
Bamann, Christian2, Author           
Bamberg, Ernst2, Author           
Busskamp, Volker1, Author
Affiliations:
1Center for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, Dresden, Germany, ou_persistent22              
2Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society, ou_2068289              

Content

show
hide
Free keywords: -
 Abstract: The widespread application of human stem-cell-derived neurons for functional studies is impeded by complicated differentiation protocols, immaturity, and deficient optogene expression as stem cells frequently lose transgene expression over time. Here we report a simple but precise Cre-loxP-based strategy for generating conditional, and thereby stable, optogenetic human stem-cell lines. These cells can be easily and efficiently differentiated into functional neurons, and optogene expression can be triggered by administering Cre protein to the cultures. This conditional expression system may be applied to stem-cell-derived neurons whenever timed transgene expression could help to overcome silencing at the stem-cell level.

Details

show
hide
Language(s): eng - English
 Dates: 2017-09-052017-10-162017-10-31
 Publication Status: Published online
 Pages: 9
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: doi:10.1038/s41598-017-14827-6
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Scientific Reports
  Abbreviation : Sci. Rep.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: London, UK : Nature Publishing Group
Pages: - Volume / Issue: 7 Sequence Number: 14450 Start / End Page: - Identifier: ISSN: 2045-2322
CoNE: https://pure.mpg.de/cone/journals/resource/2045-2322