» Articles » PMID: 22119320

Optogenetics and Thermogenetics: Technologies for Controlling the Activity of Targeted Cells Within Intact Neural Circuits

Overview
Specialties Biology
Neurology
Date 2011 Nov 29
PMID 22119320
Citations 87
Authors
Affiliations
Soon will be listed here.
Abstract

In recent years, interest has grown in the ability to manipulate, in a temporally precise fashion, the electrical activity of specific neurons embedded within densely wired brain circuits, in order to reveal how specific neurons subserve behaviors and neural computations, and to open up new horizons on the clinical treatment of brain disorders. Technologies that enable temporally precise control of electrical activity of specific neurons, and not these neurons' neighbors-whose cell bodies or processes might be just tens to hundreds of nanometers away-must involve two components. First, they require as a trigger a transient pulse of energy that supports the temporal precision of the control. Second, they require a molecular sensitizer that can be expressed in specific neurons and which renders those neurons specifically responsive to the triggering energy delivered. Optogenetic tools, such as microbial opsins, can be used to activate or silence neural activity with brief pulses of light. Thermogenetic tools, such as thermosensitive TRP channels, can be used to drive neural activity downstream of increases or decreases in temperature. We here discuss the principles underlying the operation of these two recently developed, but widely used, toolboxes, as well as the directions being taken in the use and improvement of these toolboxes.

Citing Articles

Activity Monitoring for Analysis of Sleep in .

Sitaraman D, Vecsey C, Koochagian C Cold Spring Harb Protoc. 2024; 2024(11):pdb.top108095.

PMID: 38336390 PMC: 11827337. DOI: 10.1101/pdb.top108095.


Genetically encoded mediators for sonogenetics and their applications in neuromodulation.

Wang H, Phan T, Kao C, Yeh C, Lin Y Front Cell Neurosci. 2024; 17:1326279.

PMID: 38188668 PMC: 10766825. DOI: 10.3389/fncel.2023.1326279.


Cerebellar Purkinje Cells Control Posture in Larval Zebrafish ().

Auer F, Nardone K, Matsuda K, Hibi M, Schoppik D bioRxiv. 2023; .

PMID: 37745506 PMC: 10515840. DOI: 10.1101/2023.09.12.557469.


Soft monolithic infrared neural interface for simultaneous neurostimulation and electrophysiology.

Meneghetti M, Kaur J, Sui K, Sorensen J, Berg R, Markos C Light Sci Appl. 2023; 12(1):127.

PMID: 37225682 PMC: 10209158. DOI: 10.1038/s41377-023-01164-9.


Advanced Radio Frequency Applicators for Thermal Magnetic Resonance Theranostics of Brain Tumors.

Saha N, Kuehne A, Millward J, Eigentler T, Starke L, Waiczies S Cancers (Basel). 2023; 15(8).

PMID: 37190232 PMC: 10137156. DOI: 10.3390/cancers15082303.


References
1.
Lagali P, Balya D, Awatramani G, Munch T, Kim D, Busskamp V . Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration. Nat Neurosci. 2008; 11(6):667-75. DOI: 10.1038/nn.2117. View

2.
Wyart C, Del Bene F, Warp E, Scott E, Trauner D, Baier H . Optogenetic dissection of a behavioural module in the vertebrate spinal cord. Nature. 2009; 461(7262):407-10. PMC: 2770190. DOI: 10.1038/nature08323. View

3.
Han X, Boyden E . Multiple-color optical activation, silencing, and desynchronization of neural activity, with single-spike temporal resolution. PLoS One. 2007; 2(3):e299. PMC: 1808431. DOI: 10.1371/journal.pone.0000299. View

4.
Bruegmann T, Malan D, Hesse M, Beiert T, Fuegemann C, Fleischmann B . Optogenetic control of heart muscle in vitro and in vivo. Nat Methods. 2010; 7(11):897-900. DOI: 10.1038/nmeth.1512. View

5.
Parisky K, Agosto J, Pulver S, Shang Y, Kuklin E, Hodge J . PDF cells are a GABA-responsive wake-promoting component of the Drosophila sleep circuit. Neuron. 2008; 60(4):672-82. PMC: 2734413. DOI: 10.1016/j.neuron.2008.10.042. View