Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A stem cell preparation for treating retinal degeneration and its application method

A technology of stem cell preparation and retinal degeneration, which is applied in the fields of regenerative medicine and stem cell biology, can solve the problem of stem cells losing their microenvironment, and achieve the effects of reducing immunity, simple operation, and accurate administration

Active Publication Date: 2018-09-21
奥思达干细胞有限公司
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, although the transplantation method of directly injecting the cell suspension into the subretinal space is simple and feasible, the stem cells lose the microenvironment that maintains their survival at the same time.

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 stem cell preparation for treating retinal degeneration and its application method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] Example 1 Preparation of stem cell preparation for treating retinal degeneration

[0042] A stem cell preparation for treating retinal degeneration, specifically comprising the following preparation steps:

[0043] (1) Obtain heparinized bone marrow blood;

[0044] (2) Treatment and inoculation of bone marrow blood: add LG-DMEM culture medium containing 10% FBS at a volume ratio of 1:2, mix well, and inoculate directly into the culture bottle;

[0045] (3) Cultivation of primary cells: Place the above culture flask in 5% CO 2 , 37 ℃ incubator for culture, 48h for the first time without cleaning the direct change of medium, after that, change the medium every 2 to 3 days, and wash with buffer solution PBS before changing the medium, all change the medium in full; the cells grow to 80% to 90% After fusion, the primary cells were harvested by digestion with 0.25% trypsin, which were recorded as P0 generation cells;

[0046] (4) Culture of P1 generation cells: the above ...

Embodiment 2

[0054] Example 2 Flow cytometric identification of retinal neural-like precursor cells

[0055] 1. The identification steps are as follows:

[0056] a) Collect the P4 generation cells before induction and differentiation in step 4 of the above-mentioned embodiment 1 and the P5 generation cells after induction in step 7 respectively, place them in a centrifuge tube, centrifuge at 1000 rpm for 5 min, and discard the supernatant;

[0057] b) Add 6ml of PBS to resuspend the cells, divide into 6 flow tubes, centrifuge at 1000rpm for 5min, and discard the supernatant;

[0058] c) Add 4% paraformaldehyde to fix at room temperature for 30min, centrifuge at 1000rpm for 5min, and discard the supernatant;

[0059] d) Add PBS to resuspend the cells, shake well, centrifuge at 1000rpm for 5min, and discard the supernatant;

[0060] e) Add 10% goat serum blocking solution dropwise, block at room temperature for 30min, centrifuge at 1000rpm for 5min, and discard the supernatant;

[0061] f...

Embodiment 3

[0072] Example 3 Animal Model Experiments

[0073] 1. Establishment of choroidal neovascularization (CNV) animal model

[0074] Krypton red laser was used to photocoagulate the experimental retina of mice. The laser power, photocoagulation spot diameter and exposure time were respectively 300mW, 50 μm and 0.060s to induce CNV animal model.

[0075] 2. Cell preparation transplantation test

[0076] 1) Take the stem cell preparation prepared in Example 1, and the cell concentration is 5×10 9 pcs / ml, put the prepared stem cell preparation in EP tubes, and put them in a refrigerated and insulated box at 2-15°C for use. During the experiment, the cells will precipitate after standing still, and pay attention to mixing before use;

[0077] 2) Take one experimental rat and weigh it;

[0078] 3) Anesthetized by intraperitoneal injection of 3% pentobarbital sodium 30mg / kg;

[0079] 4) 0.5% dicaine was instilled as a corneal surface anesthetic, and compound tropicamide was instilled...

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 provides a stem cell and a preparation for treating retinosis. Through optimum culture and induced differentiation on mesenchymal stem cells, the efficiency for differentiating the cell into the retina nerve precursor cell is improved; the similar effect to that of the retina precursor cell is achieved in the aspect of the transplantation effect, so that the retina function in the transplantation region is effectively improved; an ideal cell source is provided for the treatment of retinosis diseases through stem cell transplantation; high superiority is realized. A preparation method of the stem cell preparation provided by the invention has the advantages that the preparation process of the stem cell product obtained through separation, culture, posterity pass-down and induction is simple and reliable; the repeatability is good. A use method of the stem cell preparation for treating retinosis provided by the invention belongs to a cell replacing method with the advantages that the operation is simple, the popularization is convenient, and the injury is small. Wide application prospects are realized. The method belongs to the best path for treating the retinosis type degenerative diseases and rescuing the vision.

Description

technical field [0001] The invention relates to the fields of regenerative medicine and stem cell biotechnology, and relates to a stem cell preparation for treating retinal degeneration and a use method thereof. Background technique [0002] The thickness of the human retina is about 0.1-0.5 mm. Histologically, it is divided into 10 layers, of which there are mainly 4 layers of cells, which are pigment epithelial cell layer, visual cell layer, bipolar cell layer and ganglion from outside to inside. cell layer. The retinal pigment epithelium is closely connected with the choroid and is composed of pigment epithelial cells (retinal pigment epitheium, RPE). The normal RPE is a single layer of cells with polarity, located in the outermost layer of the retina. It is a highly metabolically active layer of cells that supports and nourishes photoreceptor cells, shades, dissipates heat, and regenerates and repairs. Its main functions include transshipment of nutrients, recycling of...

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): C12N5/0775C12N5/0797A61K35/30A61P27/02
Inventor 周萱王云娟
Owner 奥思达干细胞有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com