Transgenic Mouse Models Enabling Photolabeling of Individual Neurons In Vivo
Author(s) -
Manuel Peter,
Brice Bathellier,
Bruno M. Fontinha,
Pinelopi Pliota,
Wulf Haubensak,
Simon Rumpel
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0062132
Subject(s) - in vivo , neuroscience , green fluorescent protein , soma , transgene , optogenetics , genetically modified mouse , biology , biological neural network , electrophysiology , in vitro , systems neuroscience , cellular neuroscience , microbiology and biotechnology , gene , central nervous system , genetics , oligodendrocyte , myelin
One of the biggest tasks in neuroscience is to explain activity patterns of individual neurons during behavior by their cellular characteristics and their connectivity within the neuronal network. To greatly facilitate linking in vivo experiments with a more detailed molecular or physiological analysis in vitro , we have generated and characterized genetically modified mice expressing photoactivatable GFP (PA-GFP) that allow conditional photolabeling of individual neurons. Repeated photolabeling at the soma reveals basic morphological features due to diffusion of activated PA-GFP into the dendrites. Neurons photolabeled in vivo can be re-identified in acute brain slices and targeted for electrophysiological recordings. We demonstrate the advantages of PA-GFP expressing mice by the correlation of in vivo firing rates of individual neurons with their expression levels of the immediate early gene c-fos . Generally, the mouse models described in this study enable the combination of various analytical approaches to characterize living cells, also beyond the neurosciences.
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