Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

A kind of corneal limbal stem cell serum-free medium and culture method thereof

A serum-free medium and limbal stem cell technology, applied in the field of stem cell culture, can solve the problems of unsatisfactory culture effect, stem cell proliferation speed, stem cell purity and quantity, etc., to achieve rapid and stable cell source, improve purity and stability , Facilitate the effect of cell attachment

Active Publication Date: 2020-03-17
ZHONGSHAN OPHTHALMIC CENT SUN YAT SEN UNIV
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Serum-free medium has the characteristics of clear components, but the existing serum-free medium has problems such as unsatisfactory culture effect, unsatisfactory proliferation speed of stem cells, and unsatisfactory purity and quantity of stem cells after culture.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of corneal limbal stem cell serum-free medium and culture method thereof
  • A kind of corneal limbal stem cell serum-free medium and culture method thereof
  • A kind of corneal limbal stem cell serum-free medium and culture method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0065] 1. A serum-free culture medium for limbal stem cells

[0066] A serum-free medium for limbal stem cells, consisting of the following components:

[0067] 216 mL Ham's F12, 216 mL DMEM, 5 mL 100× penicillin-streptomycin double antibody solution, 1 mL human recombinant EGF stock solution, 500 μL insulin stock solution, 500 μL vitamin C stock solution, 500 μL 3,3', 5-triiodo-L-thyronine stock solution, 500 μL hydrocortisone stock solution, 1 μL forskolin stock solution, 0.5 μL manganese sulfate monohydrate, 0.5 μL sodium selenite, 500 μL silicon metasilicate sodium phosphate, 0.5 μL ammonium metavanadate, 0.5 μL nickel chloride hexahydrate, 0.5 μL stannous chloride dihydrate, 0.5 μL ethanolamine, 500 μL phosphoethanolamine, 0.5 μL ammonium molybdate tetrahydrate, 2.7 g 4-hydroxyethyl piperazine ethanesulfonic acid, 10 g bovine serum albumin, 5 mL lipid concentrate and 50 mL serum replacement.

[0068] The concentration of each added component was 10 ng / mL human recombina...

Embodiment 2

[0081] Example 2 Medium formula

[0082] The experimental method is the same as in Example 1, the only difference is that the concentration of each added component in the serum-free medium of limbal stem cells used in this example is:

[0083] 10 ng / mL human recombinant EGF, 10 μg / mL insulin, 5×10 -9 M 3-iodothyronine, 0.2 μg / mL hydrocortisone, 2×10 -5 M Forskolin, 0.5×10 -9 M manganese sulfate monohydrate, 5×10 -7 M sodium selenite, 0.1×10 -3 M sodium metasilicate, 8×10 -6 M ammonium metavanadate, 3×10 -10 M nickel chloride hexahydrate, 8×10 -10 M stannous chloride dihydrate, 3×10 -7 M ethanolamine, 8×10 -6 M Phosphoethanolamine, 1×10 -9 M ammonium molybdate tetrahydrate, 8 g / L 4-hydroxyethylpiperazineethanesulfonic acid, 20 μg / mL vitamin C, 3% bovine serum albumin, 0.5% lipid concentrate, and 15% serum replacement.

Embodiment 3

[0084] Embodiment 3 culture medium formula

[0085] The experimental method is the same as in Example 1, the only difference is that the concentration of each added component in the serum-free medium of limbal stem cells used in this example is:

[0086] 20 ng / mL human recombinant EGF, 5 μg / mL insulin, 1×10 -9 M 3-iodothyronine, 1 μg / mL hydrocortisone, 0.5×10 -5 M Forskolin, 2×10 -9 M manganese sulfate monohydrate, 10×10 -7 M sodium selenite, 1×10 -3 M sodium metasilicate, 3×10 -6 M ammonium metavanadate, 8×10 -10 M Nickel chloride hexahydrate, 3×10 -10 M stannous chloride dihydrate, 8×10 -7 M ethanolamine, 3×10 -6 M Phosphoethanolamine, 6×10 -9 M ammonium molybdate tetrahydrate, 2 g / L 4-hydroxyethylpiperazineethanesulfonic acid, 50 μg / mL vitamin C, 1% bovine serum albumin, 2% lipid concentrate, and 5% serum replacement.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a serum-free culture medium for limbal stem cells and a culture method thereof. It contains basal medium and additional components; wherein, the additional components include: human recombinant EGF, insulin, 3,3', 5-triiodo-L-thyronine, hydrocortisone, forskolin element, manganese sulfate monohydrate, sodium selenite, sodium metasilicate, ammonium metavanadate, nickel chloride hexahydrate, stannous chloride dihydrate, ethanolamine, phosphoethanolamine, ammonium molybdate tetrahydrate, 4‑hydroxyethyl piperazine ethanesulfonic acid, vitamin C, bovine serum albumin, lipid concentrate and serum replacement. The serum-free medium of the present invention does not contain fetal bovine serum and any animal-derived components, can provide sufficient nutrition and a good environment for cell growth and proliferation, effectively replace the role of serum, and the cells grow well, and the purity and stability of the cells are improved. It provides a rapid and stable source of cells for research on the specific mechanism of limbal stem cells and transplantation therapy, and has broad prospects for clinical application.

Description

technical field [0001] The invention belongs to the technical field of stem cell culture. More specifically, it relates to a serum-free culture medium for limbal stem cells and a culture method thereof. Background technique [0002] The limbus is the junction of the cornea, conjunctiva, and sclera, and the distinguishing mark from the cornea is the termination of Bowman's membrane; the distinguishing mark from the conjunctiva is that it does not contain goblet cells and is about 1 to 2 mm wide, where there are only epithelial layers and stromal layer; its epithelial cell layer contains 10 layers of cells, arranged irregularly, and the cells are small cylindrical, with deeply stained nuclei; the deep stromal cells are a layer of small cylindrical or cuboidal cells, with oval nuclei, and the surface In parallel, papillae form at the base, forming a special "palisade"-like epithelial structure, which contains pigment and rich vascular network, and is closely connected with the...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/0797
CPCC12N5/0623C12N2500/05C12N2500/20C12N2500/36C12N2500/38C12N2500/42C12N2500/46C12N2500/90C12N2501/11C12N2501/33C12N2501/39C12N2500/30
Inventor 欧阳宏朱进
Owner ZHONGSHAN OPHTHALMIC CENT SUN YAT SEN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products