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Improved method for efficient imaging of intracellular Cl− with Cl-Sensor using conventional fluorescence setup

Overview of attention for article published in Frontiers in Molecular Neuroscience, January 2013
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Title
Improved method for efficient imaging of intracellular Cl− with Cl-Sensor using conventional fluorescence setup
Published in
Frontiers in Molecular Neuroscience, January 2013
DOI 10.3389/fnmol.2013.00007
Pubmed ID
Authors

Perrine Friedel, Piotr Bregestovski, Igor Medina

Abstract

Chloride (Cl(-)) homeostasis is known to be fundamental for central nervous system functioning. Alterations in intracellular Cl(-) concentration ([Cl(-)]i) and changes in the efficacy of Cl(-) extrusion are involved in numerous neurological disorders. Therefore, there is a strong need for studies of the dynamics of [Cl(-)]i in different cell types under physiological conditions and during pathology. Several previous works reported having successfully achieved recording of [Cl(-)]i using genetically encoded Cl-Sensor that is composed of the cyan fluorescent protein (CFP) and Cl(-)-sensitive mutant of the yellow fluorescent protein (YFPCl). However, all reported works were performed using specially designed setups with ultra-sensitive CCD cameras. Our multiple attempts to monitor Cl(-)-dependent fluorescence of Cl-Sensor using conventional epifluorescence microscopes did not yield successful results. In the present work, we have analysed the reason of our failures and found that they were caused by a strong inactivation of the YFPCl component of Cl-Sensor during excitation of the CFP with 430 nm light. Based on the obtained results, we reduced 20-fold the intensity of the 430 nm excitation and modified the recording protocol that allows now stable long-lasting ratiometric measurements of Cl-Sensor fluorescence in different cell types including cultured hippocampal neurons and their tiny dendrites and spines. Simultaneous imaging and patch clamp recording revealed that in mature neurons, the novel protocol allows detection of as little as 2 mM changes of [Cl(-)]i from the resting level of 5-10 mM. We demonstrate also a usefulness of the developed [Cl(-)]i measurement procedure for large scale screening of the activity of exogenously expressed potassium-chloride co-transporter KCC2, a major neuronal Cl(-) extruder that is implicated in numerous neurological disorders and is a target for novel therapeutical treatments.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 80 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 1 1%
France 1 1%
Sweden 1 1%
Finland 1 1%
Canada 1 1%
Denmark 1 1%
Unknown 74 93%

Demographic breakdown

Readers by professional status Count As %
Researcher 22 28%
Student > Ph. D. Student 16 20%
Student > Master 10 13%
Student > Doctoral Student 7 9%
Professor > Associate Professor 6 8%
Other 14 18%
Unknown 5 6%
Readers by discipline Count As %
Agricultural and Biological Sciences 39 49%
Neuroscience 15 19%
Biochemistry, Genetics and Molecular Biology 9 11%
Medicine and Dentistry 5 6%
Engineering 2 3%
Other 3 4%
Unknown 7 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 10 April 2013.
All research outputs
#20,189,002
of 22,705,019 outputs
Outputs from Frontiers in Molecular Neuroscience
#2,441
of 2,833 outputs
Outputs of similar age
#248,733
of 280,712 outputs
Outputs of similar age from Frontiers in Molecular Neuroscience
#32
of 39 outputs
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