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Optogenetics and thermogenetics: technologies for controlling the activity of targeted cells within intact neural circuits

期刊

CURRENT OPINION IN NEUROBIOLOGY
卷 22, 期 1, 页码 61-71

出版社

CURRENT BIOLOGY LTD
DOI: 10.1016/j.conb.2011.10.023

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资金

  1. NIH [DP2OD002002, 1R01NS075421, 1R01DA029639, 1RC1MH088182, 1RC2DE020919, 1R01NS067199, 1R43NS070453]
  2. NSF [EFRI 0835878, DMS 0848804, DMS 1042134, IOS-1025307]
  3. Benesse Foundation
  4. Department of Defense CDMRP
  5. Google
  6. Harvard/MIT Joint Grants Program in Basic Neuroscience
  7. Human Frontiers Science Program
  8. MIT Alumni Class Funds
  9. MIT Intelligence Initiative
  10. MIT McGovern Institute
  11. McGovern Institute Neurotechnology
  12. MIT Media Lab
  13. MIT Mind-Machine Project
  14. MIT Neurotechnology Fund
  15. NARSAD
  16. Paul Allen Distinguished Investigator Award
  17. Alfred P. Sloan Foundation
  18. SFN Research Award for Innovation in Neuroscience
  19. Wallace H. Cooker Foundation
  20. NINDS [PO1NS044232]
  21. NIMH EUREKA [R01MH094721]
  22. Direct For Biological Sciences
  23. Division Of Integrative Organismal Systems [1025307] Funding Source: National Science Foundation
  24. Div Of Chem, Bioeng, Env, & Transp Sys
  25. Directorate For Engineering [1053233] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

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