Microfluidic reporter cell assay methods and kits thereof
Functional assays using reporter cell assays are described which probe the activity of at least one cell of interest. The ability to probe at least one cell is provided by using the microfluidic methods, devices and kits described herein. Assays combining both reporter cell signaling as well as binding assay signaling for at least one cell is also described herein.
1. A method of assaying at least one biological cell for a biological activity in a microfluidic device that contains:
a base;
a microfluidic circuit structure disposed on an inner surface of the base; and
a cover disposed over the microfluidic circuit structure,
wherein said base, said microfluidic circuit structure, and said cover together define a set of fluidically connected microfluidic circuit elements, and
wherein said circuit elements comprise:
a flow region configured to contain a flow of a first fluidic medium; and
at least one incubation chamber having a single lateral opening, wherein the single lateral opening opens laterally from the flow region, the at least one incubation chamber comprising:
at least one surface conditioned to support cell growth, viability, portability or any combination thereof;
an isolation region having a single opening, and configured to contain a second fluidic medium; and
a connection region, wherein the connection region comprises a proximal opening into the flow region and a distal opening to the isolation region, and wherein the proximal opening between the flow region and the connection region is configured to facilitate substantially only diffusion between the first fluidic medium and the second fluidic medium in the isolation region when the first fluidic medium is flowing through the flow region;
the method comprising:
introducing the at least one biological cell into the at least one incubation chamber;
introducing the at least one reporter cell into the at least one incubation chamber, wherein the at least one reporter cell is configured to produce a first detectable signal when the at least one biological cell comprises the biological activity; and
analyzing the at least one reporter cell for an activity stimulated by the presence of a biological activity of the at least one biological cell.
2. The method of claim 1 , further comprising introducing the at least one reporter cell into an isolation region of the at least one incubation chamber.
3. The method of claim 1 , further comprising introducing the at least one biological cell into the isolation region of the at least one incubation chamber.
4. The method of claim 1 , wherein the analyzing comprises incubating the at least one biological cell and the one at least one reporter cell in the at least one incubation chamber for a pre-determined period of time, thereby allowing the one at least one reporter cell to produce the first detectable signal.
5. The method of claim 4 , wherein the incubating further comprises providing the one at least one reporter cell with one or more reagents forming one or all of the components of the detectable signal of the at least one reporter cell.
6. The method of claim 1 , wherein the analyzing further comprises providing excitation light to excite a fluorophore of the first detectable signal of the at least one reporter cell.
7. The method of claim 6 , further comprising detecting the excited fluorophore.
8. The method of claim 1 , further comprising introducing at least one capture micro-object into at least the flow region.
9. The method of claim 8 , further comprising introducing one or more visualization reagents which are configured to bind to the at least one capture micro-object to produce a second detectable signal.
10. The method of claim 9 , further comprising detecting the second detectable signal.
11. The method of claim 1 , wherein introducing the at least one biological cell into the at least one incubation chamber of the microfluidic device comprises using a DEP force having sufficient strength to move the biological cell.
12. The method of claim 11 , further comprising optically actuating the DEP force.
13. The method of claim 1 , wherein the at least one biological cell is a mammalian cell.
14. The method of claim 1 , wherein the at least one biological cell is a hybridoma.
15. The method of claim 1 , wherein the at least one biological cell is a lymphocyte or a leukocyte.
16. The method of claim 1 , wherein the microfluidic device comprises at least one conditioned surface configured to support cell growth, viability, portability or any combination thereof.
17. The method of claim 1 , wherein said microfluidic circuit structure is disposed between the solid support structure and the cover such that said flow of said first fluidic medium in said flow region occurs in the same layer of the microfluidic device as said second fluidic medium disposed in said incubation chamber.
18. The method of claim 1 , wherein the cross-sectional height of the circuit elements is about 30 to about 200 microns.
19. The method of claim 1 , wherein the width of the flow region at the proximal opening ranges from about 50 to about 1000 microns.
20. A method of assaying a biological cell for a biological activity, comprising:
introducing a biological cell into an incubation chamber of a microfluidic device, wherein said microfluidic device comprises:
a base;
a microfluidic circuit structure disposed on an inner surface of the base; and
a cover disposed over the microfluidic circuit structure,
wherein said base, said microfluidic circuit structure, and said cover together define a set of fluidically connected microfluidic circuit elements, and
wherein said circuit elements comprise a flow region and said incubation chamber, said incubation chamber having a single lateral opening, wherein the single lateral opening opens laterally from said flow region and further comprising:
a surface conditioned to support cell growth, viability, portability, or any combination thereof;
an isolation region having a single opening, and configured to contain a second fluidic medium; and
a connection region, wherein the connection region comprises a proximal opening into the flow region and a distal opening to the isolation region, wherein the opening between the flow region and the connection region is configured to facilitate substantially only diffusion between the first fluidic medium flowing in the flow region and the second fluidic medium in the isolation region;
introducing a reporter cell into the incubation chamber, wherein the reporter cell is configured to produce a first detectable signal when the biological cell comprises the biological activity; and
analyzing the reporter cell for an activity stimulated by the presence of the biological activity of the biological cell.
21. The method of claim 20 , wherein the analyzing further comprises providing excitation light to excite a fluorophore of the first detectable signal of the at least one reporter cell.
22. The method of claim 20 , further comprising introducing at least one capture micro-object into at least the flow region.
23. The method of claim 20 , wherein introducing the at least one biological cell into the at least one incubation chamber of the microfluidic device comprises using a DEP force having sufficient strength to move the biological cell.