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

Culture solution and method for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells

A technology of mesenchymal stem cells and mesangial cells, applied in the field of culture medium of glomerular mesangial cells, can solve the problems of poor function, low efficiency, and long induction period, so as to reduce the types of use, improve the function of induced cells, and improve the induction The effect of differentiation efficiency

Inactive Publication Date: 2013-11-06
HARBIN YIJIAYI REGENERATIVE MEDICINE TECH
View PDF3 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The present invention establishes a new method for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells, using platelet-derived growth factor-BB and all-trans retinoic acid in combination, and at the same time supplementing type IV collagen as the extracellular matrix, Compared with the current commonly used induction methods, the induction efficiency and induction cycle are improved, and the induced glomerular mesangial precursor cells obtained have strong biological activity, which is helpful for better application in clinical transplantation, overcoming the The shortcomings of the existing inducers and induction methods such as long induction period, low efficiency, and poor function

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
  • Culture solution and method for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells
  • Culture solution and method for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells
  • Culture solution and method for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0023] 1. Preparation of human bone marrow mesenchymal stem cells.

[0024] 1) On the premise of obtaining the informed consent of healthy donors (between 5 and 36 years old), aseptically extract 5ml of bone marrow from healthy donors and place them in a collection tube containing heparin.

[0025] 2) Add Ficoll lymphocyte separation fluid to a 15ml centrifuge tube with bone marrow at a volume ratio of 1:1, and then slowly add bone marrow fluid through a syringe to keep the separation fluid and bone marrow fluid layered.

[0026] 3) Centrifuge at 2000 rpm for 15 minutes, and take out the centrifuge tube after the bone marrow cells are layered.

[0027] 4) Use the capillary to absorb the milky white bone marrow mononuclear cell liquid in the middle layer, and wash it twice with D-Hank's solution.

[0028] 5) Add low-sugar DMEM medium (containing 10% FBS, 5ng / ml bFGF, 2mM L-glutamine, penicillin 100u / ml, streptomycin 100μg / ml) to resuspend the cells, and pipette into a single c...

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 culture solution for inducing mesenchymal stem cells to differentiate into glomerular mesangial cells and an inducing method. The culture solution comprises a human platelet-derived growth factor-BB, all-trans-retinoic acid, collagen-IV and a basic medium, wherein the basic medium is a low-sugar DMEM (Dulbecco's modified eagle medium) containing 2% of horse serum and 5ng / ml of bFGF (basic fibroblast growth factor). The inducing method includes the steps: preparing the inducing culture solution; preparing the mesenchymal stem cells; coating a culture plate by the collagen-IV with the concentration of 5ug / cm<2>; inoculating the mesenchymal stem cells with the cell density of 5*103 / cm<2> into the coated culture plate and adding the inducing culture solution; changing the solution once every three days and performing inducing culture for seven days. The mesenchymal stem cells are jointly induced to differentiate into the glomerular mesangial cells by the aid of the human platelet-derived growth factor-BB, the all-trans-retinoic acid and the collagen-IV, inducing period is short, inducing efficiency is high, the glomerular mesangial cells formed by differentiation are high in functional activity, and transplantation therapy of kidney diseases such as kidney failure is facilitated.

Description

technical field [0001] The invention relates to a culture medium and an induction method for efficiently inducing the differentiation of mesenchymal stem cells into glomerular mesangial cells by using the combination of novel cell growth factor human platelet-derived growth factor-BB and all-trans retinoic acid. Background technique [0002] When various kidney diseases gradually develop into end-stage renal failure, they can usually only be treated with the help of renal replacement means, mainly dialysis and kidney transplantation. However, there are obstacles and deficiencies that are difficult to overcome in these two treatment methods. Among them, dialysis is limited to the replacement of filtration function, and does not have a series of important functions such as metabolism, secretion and maintenance of internal environment homeostasis of normal kidney. Although kidney transplantation has better therapeutic effect than dialysis, it also faces immune rejection, Due t...

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 Applications(China)
IPC IPC(8): C12N5/0775C12N5/071
Inventor 朱明东高翔
Owner HARBIN YIJIAYI REGENERATIVE MEDICINE TECH
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