Methods and devices for imaging and/or optogenetic control of light-responsive neurons

Patent metadata

Field	Value
Publication number	US-10568516-B2
Application number	US-201615735550-A
Country	US
Kind code	B2
Filing date	Jun 13, 2016
Priority date	Jun 22, 2015
Publication date	Feb 25, 2020
Grant date	Feb 25, 2020

Abstract

A method for measuring the activity of one or more excitable cells, such as neurons, in a target tissue is provided. The present method may include measuring the activity of individual, selected excitable cells by projecting one or more three dimensional (3D) multi-focal laser light patterns into a target tissue containing excitable cells adapted to emit cellular electrical activity—sensitive fluorescence, to generate a multiplexed 2D diffraction pattern of fluorescence emitted by the neurons, and resolving the multiplexed 2D diffraction pattern. Also provided herein is a system configured to perform the present method, the system including a microscope configured to project one or more 3D multi-focal laser light patterns into a target tissue using a spatial light modulator and a mirror galvanometer, and a microlens array and an image detector to record individual and multiplexed 2D diffraction patterns of light emitted from the target tissue.

First claim

What is claimed is:

1. A method for measuring the activity of excitable cells in a target tissue, the method comprising:
i) selecting a first plurality of excitable cells in a target tissue for measuring activity, wherein the excitable cells are adapted to emit fluorescence in a cellular electrical activity-sensitive manner; and
ii) measuring the activity of each of the excitable cells by:
a) illuminating the first plurality of excitable cells with spatio-temporally multiplexed three-dimensional (3D) multi-focal light patterns, thereby causing the excitable cells to emit fluorescence, wherein the 3D multi-focal light patterns are generated using a spatial light modulator and a pair of mirror galvanometers to spatially translate a field of view of the spatial light modulator on the target tissue, and wherein different subsets of excitable cells from the first plurality are illuminated among at least some of the 3D multi-focal light patterns;
b) recording, using an image detector, a multiplexed 2D diffraction pattern of the emitted fluorescence diffracted by a microlens array;
c) resolving the multiplexed 2D diffraction pattern to determine the activity of each excitable cell illuminated by the plurality of 3D multi-focal light patterns, wherein resolving the multiplexed 2D diffraction pattern comprises deconvolving the multiplexed 2D diffraction pattern using an optical model for light propagation through an emission path from the target tissue to the image detector, wherein the optical model comprises individual 2D diffraction patterns for fluorescence emitted by the first plurality of excitable cells and diffracted by the microlens array; and
d) selecting members of the different subsets of the first plurality of excitable cells based on the individual 2D diffraction patterns.

2. The method according to claim 1 , wherein the illuminating comprises projecting a plurality of 3D multi-focal light patterns sequentially into the target tissue at a rate of at most about 0.75 times a maximum switching rate of the spatial light modulator.

3. The method according to claim 1 , wherein the illuminating comprises using a mirror galvanometer.

4. The method according to claim 1 , wherein the first plurality of excitable cells comprises at least 40 cells.

5. The method according to claim 1 , wherein the different subsets of excitable cells comprise on average 90% or fewer cells than the first plurality of excitable cells.

6. The method according to claim 1 , wherein the spatio-temporally multiplexed 3D multi-focal light patterns collectively have a power at the target tissue of about 500 mW or less.

7. The method according to claim 1 , wherein measuring the activity of an individual excitable cell is performed at a frequency of from about 5 Hz to about 100 Hz.

8. The method according to claim 1 , further comprising obtaining individual 2D diffraction patterns for each of the first plurality of excitable cells in the target tissue, by
a) contacting an excitable cell of the first plurality with a laser light, thereby causing the contacted excitable cell to emit fluorescence; and
b) recording, using the image detector, a 2D diffraction pattern of the emitted fluorescence diffracted by the microlens array.

9. The method according to claim 8 , wherein the contacting comprises two-photon 2D laser scanning.

10. The method according to claim 1 , wherein the deconvolving comprises determining individual point spread functions (PSFs) for each of the individual 2D diffraction patterns and using the individual PSFs to deconvolve the multiplexed 2D diffraction pattern.

11. The method according to claim 1 , wherein the selecting members of the different subsets comprises:
comparing the individual 2D diffraction patterns among each other; and
selecting members of the different subset such that a minimum difference in the individual 2D diffraction patterns between excitable cells in any pair of the different subsets is at or above a threshold difference.

12. The method according to claim 11 , wherein the threshold difference maximizes the minimum difference.

13. The method according to claim 1 , wherein the plurality of 3D multi-focal laser light patterns are generated by spatially modulating a laser beam using the spatial light modulator.

14. The method according to claim 13 , wherein the laser beam is pulsed at a frequency of from about 100 MHz to about 500 kHz.

15. The method according to claim 13 , wherein the laser beam has an average power of about 1.0 W to about 3.0 W.

16. The method according to claim 13 , wherein the laser beam has a pulse duration of about 100 fs to about 500 fs.

17. The method according to claim 1 , wherein the selecting comprises:
scanning the target tissue using a focused laser light, to generate an image of the target tissue; and
identifying excitable cells in the image.

18. The method according to claim 17 , wherein the focused laser light is pulsed at a frequency of about 10 MHz to about 200 MHz.

19. The method according to claim 17 , wherein the focused laser light is generated using a spatial light modulator.

20. The method according to claim 1 , the image detector is a Complementary Metal Oxide Semiconductor (CMOS) detector.

21. The method according to claim 1 , wherein the excitable cells comprise neurons.

22. The method according to claim 1 , wherein the target tissue is an in vivo neuronal tissue.

23. The method according to claim 1 , wherein the target tissue is a light-scattering tissue.

24. The method according to claim 1 , wherein the excitable cells are adapted to emit fluorescence in a calcium- or voltage-sensitive manner.

25. The method according to claim 24 , wherein the excitable cells comprise an activity-sensitive fluorescent dye.

26. The method according to claim 24 , wherein the excitable cells comprise a genetically encoded, activity-sensitive fluorescent protein.

27. The method according to claim 1 , wherein the 3D multi-focal light patterns comprise light having a wavelength in the near-infrared range.

28. The method according to claim 1 , wherein the method further comprises:
stimulating the target tissue; and
measuring the activity of the first plurality of excitable cells in response to the stimulation.

29. The method according to claim 28 , wherein the target tissue comprises a second plurality of excitable cells that are adapted to hyperpolarize and/or depolarize in response to a laser light stimulus, and the stimulating comprises contacting the second plurality of excitable cells with a laser light stimulus.

30. The method according to claim 29 , wherein an excitable cell that is adapted to hyperpolarize and/or depolarize in response to a laser light stimulus is genetically modified to express one or more light-responsive polypeptides that hyperpolarize or depolarize the excitable cell when contacted by a laser light.

31. A method of regulating the activity of a plurality of excitable cells in a target tissue, comprising:
i) measuring the activity of a first plurality of activity-sensitive fluorescence-emitting excitable cells in a target tissue comprising a second plurality of excitable cells, according to the method of claim 1 ; and
ii) modulating the activity of the second plurality of excitable cells in the target tissue in response to the measur

Assignees

• Univ Leland Stanford Junior

Inventors

• Yang Samuel
• Deisseroth Karl A
• Allen William E
• Kauvar Isaac V
• Andalman Aaron S

Classifications

• G01N21/6458

  Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16) · CPC title

• A61B5/4064

  Evaluating the brain (for intracranial pressure A61B5/031; for cerebral blood gases A61B5/14553; using EEG A61B5/369) · CPC title

• G01N21/6428

  Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title

• H04N7/18

  Closed-circuit television [CCTV] systems, i.e. systems in which the video signal is not broadcast · CPC title

• G06T2207/30016

  Brain · CPC title