Adherent cell culture method

Patent metadata

Field	Value
Publication number	US-10655107-B2
Application number	US-201214346121-A
Country	US
Kind code	B2
Filing date	Sep 20, 2012
Priority date	Sep 20, 2011
Publication date	May 19, 2020
Grant date	May 19, 2020

Abstract

Provided are a method capable of evaluating adherent cells under an environment similar to an in vivo environment by a culture method similar to a two-dimensional culture, and applications thereof. An adherent cell culture method uses, as a culture chamber ( 10 ), a chamber in which two or more culture spaces each having an equivalent diameter (D) that is 1 to 5 times the diameter of a desired spheroid and each having a height (H) that is 0.3 to 5 times the equivalent diameter are arranged and a surface of each of the culture spaces has a water contact angle of 45 degrees or less. Spheroids of adherent cells are cultured in the respective culture spaces ( 11 ) arranged in the culture chamber ( 10 ).

First claim

The invention claimed is:

1. A method of culturing adherent cells, the method comprising
seeding adherent cells by injecting a culture medium containing the adherent cells into each culture space of a plurality of culture spaces within a culture chamber,
culturing the adherent cells to form spheroids of the adherent cells in each culture space,
culturing the spheroid within each culture space,
wherein:
each culture space has an equivalent diameter that is 1 to 3 times the diameter of a desired spheroid and said equivalent diameter is within the range of 100 μm to 200 μm;
each culture space has a height that is 0.5 to 2 times the equivalent diameter;
a surface of each culture space has a water contact angle of 45 degrees or less;
each culture space has either a cylindrical shape or a rectangular prism shape, and a flat culture bottom surface;
each culture space comprises a wall partitioning the adjacent culture spaces;
the culture space wall has a height equal to the height of the culture space, and a thickness in the range of 5 μm to 50 μm;
the spheroid cultured in each culture space is contained within the culture space, and does not come into contact with the spheroid in an adjacent culture space during the culturing; and
60% or more of all cultured spheroids have a diameter within a range of 5% below to 5% above an average value of diameters of the spheroids obtained after the culturing.

2. The method of claim 1 , wherein the thickness of the wall partitioning the adjacent culture spaces is in a range of 5 μm to 20 μm.

3. The method of claim 1 , wherein the thickness of the wall partitioning the adjacent culture spaces is in a range of 20 μm to 50 μm.

4. The method of claim 1 , wherein the wall partitioning the adjacent culture spaces has an angle formed between an upper surface and a side surface of the wall of 90 degrees.

5. The method of claim 1 , wherein the spheroids are cancer cells.

6. The method of claim 1 , wherein the culture chamber comprises a resin molded product comprising at least one member selected from the group consisting of an acrylic resin, a polylactic acid, a polyglycolic acid, a styrene resin, an acrylic-styrene copolymer resin, a polycarbonate resin, a polyester resin, a polyvinyl alcohol resin, an ethylene-vinylalcohol copolymer resin, a thermoplastic elastomer, a vinyl chloride resin, and a silicon resin.

7. The method of claim 1 , wherein the surface of each culture space has been processed by glass processing so that the surface has a water contact angle of 45 degrees or less.

8. The method of claim 1 , wherein the surface of each of the culture spaces is processed by forming a functional group thereon by plasma treatment so that the surface has a water contact angle of 45 degrees or less.

9. The method of claim 1 , wherein a polymer having hydrophilic and hydrophobic properties that vary depending on temperature or light is coated on the surface of each culture space.

10. The method of claim 1 , wherein a hydrophilic polymer chain that inhibits cell adhesion is immobilized on the surface of each of the culture spaces.

11. The method of claim 1 , wherein a phospholipid or a phospholipid-polymer complex is immobilized on the surface of each culture space.

12. The method of claim 1 , wherein the surface of each culture space has been processed by glass processing so that the surface has a water contact angle of 45 degrees or less, and thereafter a polymer having hydrophilic and hydrophobic properties that vary depending on temperature or light, a hydrophilic polymer chain that inhibits cell adhesion, a phospholipid, or a phospholipid-polymer complex is immobilized on the surface.

13. The method of claim 1 , wherein the surface of each culture space has been processed by forming a functional group thereon by plasma treatment so that the surface has a water contact angle of 45 degrees or less, and thereafter a polymer having hydrophilic and hydrophobic properties that vary depending on temperature or light, a hydrophilic polymer chain that inhibits cell adhesion, one of a phospholipid, or a phospholipid-polymer complex is immobilized on the surface.

14. The method of claim 2 , wherein the spheroids are cancer cells.

15. The method of claim 14 , wherein:
the culture space wall partitioning the adjacent culture spaces has an angle formed between an upper surface and a side surface of the wall of 90 degrees.

16. The method of claim 1 , wherein each culture space has a rectangular prism shape.

17. The method of claim 1 , wherein a thickness of a bottom portion of the culture chamber is 1 mm or less.

18. A method of culturing adherent cells, the method comprising culturing a spheroid of adherent cells in each of a plurality of culture spaces within a culture chamber,
wherein:
each culture space has an equivalent diameter that is 1 to 3 times the diameter of a desired spheroid;
each culture space has a height that is 0.5 to 2 times the equivalent diameter;
each culture space has walls partitioning the adjacent culture spaces, and the walls have a thickness in the range of 5 μm to 50 μm;
a surface of each culture space has a water contact angle of 45 degrees or less;
a polymer having hydrophilic and hydrophobic properties that vary depending on light is coated on the surface of each of culture space;
the thickness of a bottom portion of the culture chamber is 1 mm or less;
the spheroid in each culture space is contained within the culture space, and does not come into contact with the spheroid in an adjacent culture space during the culturing; and
60% or more of all cultured spheroids have a diameter within a range of 5% below to 5% above an average value of diameters of the spheroids obtained after the culturing.

Assignees

• Corning Inc

Inventors

• Ejiri Yoko
• Ayano Satoru
• Hosoda Masaya
• Tazaki Go

Classifications

• C12M23/20

  Material Coatings (immunocoatings C12M25/00) · CPC title

• C12N5/0693 Primary

  Tumour cells; Cancer cells · CPC title

• C12M23/12 Primary

  Well or multiwell plates (C12M25/04 takes precedence) · CPC title

• C12N2535/00

  Supports or coatings for cell culture characterised by topography · CPC title

• C12N2533/20

  Small organic molecules · CPC title