Co-culture device assembly
An insert device and co-culture device assembly incorporating the insert device, which includes an insert chamber with two fluid impermeable side walls that extend from a microporous bottom to an open top to form an inner cavity. The first side wall is shaped to form a convex arc that follows between about half of a circumference of the well and less than an entire circumference of the well. The second side wall joins ends of the first side wall and protrudes inward towards a center of the convex arc. A flange extends outward from or beneath the top and is notched to form a gap adjacent to the second side wall, which forms an access port allowing access to the lower chamber with a micropipette tip when the insert device is inserted into a well of a single or multi-well plate.
1. A co-culture device assembly comprising an insertion device suspended above a bottom surface of a well to form an upper chamber for housing cells over a lower chamber, wherein the insertion device is characterized as:
a) an insert chamber comprising two fluid impermeable side walls extending from a microporous bottom to an open top to form an inner cavity, characterized in that first and second side walls are each shaped convex and are joined to one another at each end, wherein the first and second side walls are of a same height; and
b) a flange extending outward from or beneath the top of the insert chamber and suspending the microporous bottom above the bottom surface of the well to form the upper and lower chambers, the flange notched to form a gap providing access to the lower chamber but not the top chamber, wherein a bottom surface of the flange comprises an upward extending recess that recesses into the flange for preventing or reducing liquid migration across the bottom surface of the flange.
2. The assembly according to claim 1 , wherein the flange follows the perimeter of the first sidewall.
3. The insert device according to claim 1 , wherein the open top comprises an outer ridge extending above the flange.
4. The insert device according to claim 1 , wherein the two side walls taper from top to bottom.
5. The insert device according to claim 1 , wherein the microporous bottom comprises a porous biocompatible membrane that prevents passage of eukaryotic cells.
6. The insert device according to claim 1 , wherein the insert chamber is a kidney-shaped cylinder.
7. The insert device according to claim 1 , wherein the first side wall follows about two thirds of the circumference of the well.
8. The insert device according to claim 7 , wherein the gap protrudes inward.
9. The assembly according to 1 , wherein a plurality of insert devices are joined together by neighboring flanges to form an insert tray and a plurality of wells are joined together to form a multi-well plate.
10. The assembly according to claim 9 , wherein at least two of the gaps are joined to form a common gap.
11. The assembly according to 1 , wherein the bottom of the well comprises electrodes.
12. A system for monitoring a cell culture comprising providing the assembly according to 1 coupled to a means for measuring a cell culture characteristic.
13. The system according to claim 12 , wherein the bottom of the well comprises electrodes and the means for measuring the cell culture characteristic is an impedance analyzer, optionally coupled to software.
14. The system according to claim 12 , wherein the means for measuring the cell culture characteristic is an optical detection device for measuring an optical property or an imaging device for producing a cell culture image.
15. A method of monitoring a cell culture comprising:
a) providing the system according to claim 12 ;
b) adding a first cell population to the well and a second cell population to the inner cavity of the insert chamber;
c) inserting the insert device into the well to form upper and lower chambers, each having separate cell populations; and
d) measuring the cell culture characteristic.
16. The method according to claim 15 , wherein the first population is population of target cells and the second population is a population of effector cells.
17. The method according to claim 16 , wherein the cell characteristic is cell viability or cell proliferation.
18. The method according to claim 17 , wherein the means for measuring the cell culture characteristic measures an optical property or an electrical property of the bottom chamber.