Journal Article DZNE-2024-00921

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Aberrant hippocampal Ca2+ microwaves following synapsin-dependent adeno-associated viral expression of Ca2+ indicators.

 ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;

2024
eLife Sciences Publications Cambridge

eLife 13, RP93804 () [10.7554/eLife.93804]

This record in other databases:    

Please use a persistent id in citations: doi:

Abstract: Genetically encoded calcium indicators (GECIs) such as GCaMP are invaluable tools in neuroscience to monitor neuronal activity using optical imaging. The viral transduction of GECIs is commonly used to target expression to specific brain regions, can be conveniently used with any mouse strain of interest without the need for prior crossing with a GECI mouse line, and avoids potential hazards due to the chronic expression of GECIs during development. A key requirement for monitoring neuronal activity with an indicator is that the indicator itself minimally affects activity. Here, using common adeno-associated viral (AAV) transduction procedures, we describe spatially confined aberrant Ca2+ microwaves slowly travelling through the hippocampus following expression of GCaMP6, GCaMP7, or R-CaMP1.07 driven by the synapsin promoter with AAV-dependent gene transfer in a titre-dependent fashion. Ca2+ microwaves developed in hippocampal CA1 and CA3, but not dentate gyrus nor neocortex, were typically first observed at 4 wk after viral transduction, and persisted up to at least 8 wk. The phenomenon was robust and observed across laboratories with various experimenters and setups. Our results indicate that aberrant hippocampal Ca2+ microwaves depend on the promoter and viral titre of the GECI, density of expression, as well as the targeted brain region. We used an alternative viral transduction method of GCaMP which avoids this artefact. The results show that commonly used Ca2+-indicator AAV transduction procedures can produce artefactual Ca2+ responses. Our aim is to raise awareness in the field of these artefactual transduction-induced Ca2+ microwaves, and we provide a potential solution.

Keyword(s): Animals (MeSH) ; Dependovirus: genetics (MeSH) ; Synapsins: metabolism (MeSH) ; Synapsins: genetics (MeSH) ; Calcium: metabolism (MeSH) ; Hippocampus: metabolism (MeSH) ; Mice (MeSH) ; Genetic Vectors (MeSH) ; Transduction, Genetic (MeSH) ; Promoter Regions, Genetic (MeSH) ; Mice, Inbred C57BL (MeSH) ; Male (MeSH) ; AAV ; GCaMP ; GECI ; in vivo ; mouse ; neuroscience ; Synapsins ; Calcium

Classification:

Contributing Institute(s):
  1. Neuroimmunology and Imaging (AG Fuhrmann)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Appears in the scientific report 2024
Database coverage:
Medline ; Creative Commons Attribution CC BY 4.0 ; DOAJ ; OpenAccess ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; DOAJ Seal ; Ebsco Academic Search ; Essential Science Indicators ; Fees ; IF >= 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection ; Zoological Record
Click to display QR Code for this record

The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > BN DZNE > BN DZNE-AG Fuhrmann
Full Text Collection
Public records
Publications Database

 Record created 2024-07-26, last modified 2024-08-11


OpenAccess:
Download fulltext PDF Download fulltext PDF (PDFA)
External link:
Download fulltextFulltext by Pubmed Central
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)