| Literature DB >> 30377377 |
Laura Alberio1, Andrea Locarno2, Andrea Saponaro1, Edoardo Romano1, Valérie Bercier3, Shahad Albadri3, Federica Simeoni1, Silvia Moleri1, Silvia Pelucchi4,5, Alessandro Porro1, Elena Marcello4, Noemi Barsotti6, Kerri Kukovetz7, Arjen J Boender2, Andrea Contestabile8, Shizhen Luo9, Aubin Moutal9, Yingshi Ji9, Giulia Romani10, Monica Beltrame1, Filippo Del Bene3, Monica Di Luca4, Rajesh Khanna9, Henry M Colecraft11, Massimo Pasqualetti6,12, Gerhard Thiel7, Raffaella Tonini13, Anna Moroni14,15,16.
Abstract
Currently available inhibitory optogenetic tools provide short and transient silencing of neurons, but they cannot provide long-lasting inhibition because of the requirement for high light intensities. Here we present an optimized blue-light-sensitive synthetic potassium channel, BLINK2, which showed good expression in neurons in three species. The channel is activated by illumination with low doses of blue light, and in our experiments it remained active over (tens of) minutes in the dark after the illumination was stopped. This activation caused long periods of inhibition of neuronal firing in ex vivo recordings of mouse neurons and impaired motor neuron response in zebrafish in vivo. As a proof-of-concept application, we demonstrated that in a freely moving rat model of neuropathic pain, the activation of a small number of BLINK2 channels caused a long-lasting (>30 min) reduction in pain sensation.Entities:
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Year: 2018 PMID: 30377377 PMCID: PMC6834437 DOI: 10.1038/s41592-018-0186-9
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547