This invention relates to cell isolation and manipulation in general, and more particularly to the controlled positioning of individual cells at precise locations on a substrate.
Current high-throughput screening of cell function and heterogeneity, and in vitro cell-cell communication studies, generally require routine generation of large-scale, single-cell arrays with high precision and efficiency, single-cell resolution, multiple cell types, and maintenance of cell viability and function. Several approaches are currently used in an effort to achieve this goal, e.g., inkjet cell printing (where individual cells are printed to a substrate in a free-flying droplet), surface engineering (where microfabrication and biochemical functionalization are combined to produce defined regions for selected cell adhesion), and physical constraints (where cell-capturing elements are used to isolate individual cells). However, for a variety of reasons, none of the approaches developed to date are completely satisfactory.
Thus, a new approach is needed for the controlled positioning of individual cells at precise locations on a substrate.
The present invention provides a new approach for the controlled positioning of individual cells at precise locations on a substrate.
More particularly, the present invention provides a cell positioning structure having a plurality of surface channels formed therein, with the surface channels having single-cell traps disposed therein. The cell positioning structure is releasably assembled to a substrate (e.g., a commercial cell culture dish) so that the surface channels of the cell positioning structure cooperate with the substrate to provide microfluidic pathways through the assembly, with the microfluidic pathways incorporating the aforementioned single-cell traps. A slurry of cells is flowed through the microfluidic pathways of the assembly so that individual cells are captured in the single-cell traps, whereby to position the captured cells adjacent to the substrate with high positional precision. The captured cells are incubated so that the captured cells adhere to the substrate, and then the cell positioning structure is detached from the substrate, leaving individual cells disposed at precise locations on the substrate.
In one preferred form of the present invention, there is provided apparatus for single cell patterning, said apparatus comprising:
a structure comprising a surface channel formed therein, said surface channel being connected to an inlet and an outlet; and
a cell trap disposed in said surface channel, said cell trap comprising a body defining a flow diverter for diverting flow passing by said cell trap into a wide path or a narrow path, and said body and said structure together defining a well for capturing a cell diverted by said flow diverter toward said narrow path.
In another preferred form of the present invention, there is provided apparatus for single cell patterning, said apparatus comprising:
a structure comprising a surface channel formed therein, said surface channel being connected to an inlet and an outlet;
a cell trap disposed in said surface channel, said cell trap comprising a body defining a flow diverter for diverting flow passing by said cell trap into a wide path or a narrow path, and said body and said structure together defining a well for capturing a cell diverted by said flow diverter toward said narrow path; and
a substrate comprising a base, said structure being releasably mountable to said substrate so that a cell captured by said cell trap may be caused to adhere to said base.
In another preferred form of the present invention, there is provided a method for patterning individual cells on a substrate, said method comprising:
providing a structure comprising a surface channel formed therein, and comprising a cell trap disposed in said surface channel;
attaching the substrate to said structure so as to form an assembly, with said surface channel of said structure cooperating with said substrate to provide a microfluidic pathway through said assembly;
flowing a slurry of cells through said microfluidic pathway of said assembly so that an individual cell is captured in said cell trap;
causing said captured cell to adhere to said substrate; and
detaching said structure from said substrate so as to leave the captured cell disposed on said substrate.
In another preferred form of the present invention, there is provided apparatus for single cell patterning, said apparatus comprising:
a structure comprising a plurality of surface channels formed therein, said surface channels being connected to an inlet and an outlet; and
a plurality of cell traps disposed in said surface channels, each of said cell traps comprising a body defining a flow diverter for diverting flow passing by said cell trap into a wide path or a narrow path, and said body and said structure together defining a well for capturing a cell diverted by said flow diverter toward said narrow path.
In another preferred form of the present invention, there is provided apparatus for single cell patterning, said apparatus comprising:
a structure comprising a plurality of surface channels formed therein, said surface channels being connected to an inlet and an outlet;
a plurality of cell traps disposed in said surface channels, each of said cell traps comprising a body defining a flow diverter for diverting flow passing by said cell trap into a wide path or a narrow path, and said body and said structure together defining a well for capturing a cell diverted by said flow diverter toward said narrow path; and
a substrate comprising a base, said structure being releasably mountable to said substrate so that cells captured by said cell traps may be caused to adhere to said base.
In another preferred form of the present invention, there is provided a method for patterning individual cells on a substrate, said method comprising:
providing a structure comprising a plurality of surface channels formed therein, and comprising a plurality of cell traps disposed in said surface channels;
attaching the substrate to said structure so as to form an assembly, with said surface channels of said structure cooperating with said substrate to provide a microfluidic pathway through said assembly;
flowing a slurry of cells through said microfluidic pathway of said assembly so that individual cells are captured in said cell traps;
causing said captured cells to adhere to said substrate; and
detaching said structure from said substrate so as to leave the captured cells disposed on said substrate.
These and other objects and features of the present invention will be more fully disclosed or rendered obvious by the following detailed description of the preferred embodiments of the invention, which is to be considered together with the accompanying drawings wherein like numbers refer to like parts, and further wherein:
The present invention provides a new approach for the controlled positioning of individual cells at precise locations on a substrate.
More particularly, the present invention provides a cell positioning structure having a plurality of surface channels formed therein, with the surface channels having single-cell traps disposed therein. The cell positioning structure is releasably assembled to a substrate (e.g., a commercial cell culture dish) so that the surface channels of the cell positioning structure cooperates with the substrate to provide microfluidic pathways through the assembly, with the microfluidic pathways incorporating the aforementioned single-cell traps. A slurry of cells is flowed through the microfluidic pathways of the assembly so that individual cells are captured in the single-cell traps, whereby to position the captured cells adjacent to the substrate with high positional precision. The captured cells are incubated so that the captured cells adhere to the substrate, and then the cell positioning structure is detached from the substrate, leaving individual cells disposed at precise locations on the substrate.
In one preferred form of the present invention, and looking now at
As seen in
In one preferred form of the invention, surface channel 20 may have a width of 40 μm, wide path 30 may have a width of 22 μm, narrow path 35 may have a width of 3 μm, flow diverter 40 may have a width of 6 μm and well 45 may have a width of 12 μm and a depth of 10 μm.
On account of the foregoing, and looking now at
In accordance with the present invention, and looking now at
If desired, captured cells C may be adhered to substrate 50 in ways other than incubation, and/or in ways in addition to incubation. By way of example but not limitation, substrate 50 may have its base 55 functionalized in ways well known in the art so that captured cells C adhere to substrate 50, e.g., by applying an adhesive substance to substrate 50.
It will be appreciated that cell positioning structure 5 and substrate 50 are configured so that, when cell positioning structure 5 is releasably assembled to substrate 50, the cells C captured in single-cell traps 25 are disposed an appropriate distance from base 55 such that the captured cells C may be adhered to, and thereafter transferred to, substrate 50.
Thus it will be seen that, by providing cell positioning structure 5 with a plurality of surface channels 20 having a plurality of single-cell traps 25 disposed therein, with single-cell traps 25 being disposed on cell positioning structure 5 in a predetermined, precision array, individual cells may be precisely positioned on substrate 50 in a corresponding predetermined precision array.
In one preferred form of the invention, cell positioning structure 5 may be fabricated in the following manner. The design is drawn with CAD software and printed out as glass photomasks (Photo Sciences Inc.). Polydimethylsiloxane (PDMS) molds are then fabricated by standard photolithography and elastomer molding. In one preferred form of the invention, SPR 220-7 positive photoresist (MicroChem Corp.) is used to fabricate 12 μm thick channels and SU-8 3025 negative photoresist (MicroChem Corp.) is used to fabricate 17-μm thick channels. SPR 220-7 photoresist is spin-coated onto a 4 inch silicon wafer (Silicon Quest International Inc.) at 1,500 rpm for 40 seconds to form a layer approximately 12 μm thick. After baking at 75° C. for 3 minutes, and then at 115° C. for 5 minutes, the wafer is cooled, exposed to UV light for 7 seconds, and developed. SU-8 3025 photoresist is spin-coated onto a 4 inch silicon wafer at 4,000 rpm for 60 seconds to form a layer approximately 17 μm inch thickness. After soft baking at 65° C. for 2 minutes and then at 95° C. for 10 minutes, the wafer is cooled and exposed to UV light for 6 seconds. It is then heated for post-exposure baking at 65° C. for 1 minute and then at 95° C. for 3 minutes. After cooling down, the wafer is developed and heated for hard baking at 135° C. for 20 minutes. Finally PDMS (10A:1B, Dow Corning Corp.) is poured onto the photoresist mold and heated at 75° C. for 30 minutes. After curing, the PDMS is peeled off, cut to the appropriate size, and then punched to form cell positioning structure 5.
It will be appreciated that, by varying the disposition of surface channels 20 and single-cell traps 25 on cell positioning structure 5, the disposition of individual cells on substrate 50 may be similarly varied. See, for example,
It is also possible to practice the present invention with cell traps capable of capturing more than one cell. More particularly, in the embodiments shown in
By way of example but not limitation, and looking now at
In order to permit continuous fluid flow into well 80 (i.e., via narrow path 70), well 80 preferably comprises a filter 85. Filter 85 generally comprises walls 90 spaced from body 72 and the side wall of the surface channel so as to provide gaps 95 therebetween. A plurality of openings 100 are formed in walls 90 so as to provide fluid communication between well 80 and gaps 95. Gaps 95 communicate with an outlet 110 which is in fluid communication with surface channel 20. By virtue of this construction, fluid can flow through narrow path 70, into well 80, through openings 100, into gaps 95, through outlet 110 and back into surface channel 20. However, if a cell is diverted into narrow path 70 and into well 80, the cell will be too large to pass through openings 100 and into gaps 95, and thus will be retained in well 80.
On account of the foregoing, when a slurry of cells passes down a surface channel 20, flow diverter 75 causes some of the flow to pass down wide path 65 and some of the flow to pass down narrow path 70. Significantly, as the cells in the slurry encounter flow diverter 75 of 1×N cell trap 60, most of the cells follow wide path 65 and pass by 1×N cell trap 60. However, in some instances, a single cell C will be diverted into well 80 of 1×N cell trap 60, whereby to form a 1×N array of cells. Again, note that cells C may cluster in wide path 65 adjacent to flow diverter 75 as they try to move through wide path 65, and this clustering of cells may assist in one cell at a time being diverted into well 80.
By way of further example but not limitation, and looking now at
In order to permit continuous fluid flow into well 135 (i.e., via narrow path 125), well 135 preferably comprises a filter 140. Filter 140 generally comprises walls 145 spaced from body 127 and the side wall of the surface channel so as to provide gaps 150 therebetween. A plurality of openings 155 are formed in walls 145 so as to provide fluid communication between well 135 and gaps 150. Gaps 150 communicate with an outlet 160 which is in fluid communication with surface channel 20. By virtue of this construction, fluid can flow through narrow path 125, into well 135, through openings 155, into gaps 150, through outlet 160 and back into surface channel 20. However, if a cell is diverted into narrow path 125 and into well 135, the cell will be too large to pass through openings 155 and into gaps 150 and thus will be retained in well 135.
On account of the foregoing, when a slurry of cells passes down a surface channel 20, flow diverter 130 causes some of the flow to pass down wide path 120 and some of the flow to pass down narrow path 125. Significantly, as cells in the slurry encounter flow diverter 130 of N1×N2 cell trap 115, most of the cells follow wide path 120 and pass by N1×N2 cell trap 115. However, in some instances, a single cell will be diverted into well 135 of N1×N2 cell trap 115, whereby to form an N1×N2 array of cells. Again, note that cells may cluster in wide path 120 adjacent to diverter 135 as they try to move through wide path 120, and this clustering of cells may assist in a single cell at a time being diverted into well 135.
As seen in
It should be understood that many additional changes in the details, materials, steps and arrangements of parts, which have been herein described and illustrated in order to explain the nature of the present invention, may be made by those skilled in the art while still remaining within the principles and scope of the invention.
This patent application claims benefit of pending prior U.S. Provisional Patent Application Ser. No. 61/930,813, filed Jan. 23, 2014 by The Methodist Hospital and Lidong Qin et al. for SINGLE CELL PATTERNING AND BLOCK PRINTING (Attorney's Docket No. METHODIST-0810 PROV), which patent application is hereby incorporated herein by reference.
Filing Document | Filing Date | Country | Kind |
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PCT/US15/12736 | 1/23/2015 | WO | 00 |
Number | Date | Country | |
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61930813 | Jan 2014 | US |