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A kind of naked mole rat Schwann cell culture method

A technology of Schwann cells and culture methods, applied in the field of cell biology, can solve problems such as inapplicability to naked mole rats, and achieve high repeatability and simple operation methods

Active Publication Date: 2021-01-26
SECOND MILITARY MEDICAL UNIV OF THE PEOPLES LIBERATION ARMY +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, in the prior art, no matter the methods for the separation, purification and cultivation of Schwann cells in mice or rats are not applicable to naked mole rats, there is no relevant report on the methods for separation, purification and cultivation of Schwann cells in naked mole rats at present.

Method used

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  • A kind of naked mole rat Schwann cell culture method
  • A kind of naked mole rat Schwann cell culture method
  • A kind of naked mole rat Schwann cell culture method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Example 1: Separation, purification and culture of naked mole rat Schwann cells

[0039] 1. Experimental materials

[0040] Naked mole rats at embryonic days 58-65 were provided by the Experimental Animal Center of the Second Military Medical University of the Chinese People's Liberation Army. DNase I was purchased from Solarbio Biotechnology Co., Ltd., trypsin, L-polylysine, PDGFa, penicillin-streptomycin mixture, etc. were purchased from Sigma Company, DMEM, low-sugar DMEM, Australian-sourced fetal bovine serum, etc. were purchased from Thermo Fisher Scientific company, petri dishes, T25 and T75 culture flasks were purchased from Corning company.

[0041] The mixed nerve cell medium is a low-sugar DMEM medium containing 15% imported fetal bovine serum by volume.

[0042] Schwann cell purification medium is Neurobasal containing 2% B27 by volume fraction and PDGFa with mass volume fraction 0.01 mg / ml added.

[0043] 2. Isolation, purification and culture of naked mo...

Embodiment 2

[0046] Example 2: Identification of Naked Mole Rat Schwann Cells

[0047] Identification of the naked mole-rat Schwann cells obtained in Example 1: the Schwann cells in the proliferation medium were fixed with 4% paraformaldehyde, and identified in combination with morphological identification, immunochemical refinement and other methods.

[0048] 1. Cell morphology identification:

[0049] The identification method was described in references (Wenjing Yang, Lin Xiao, Cui Li, Xiuyun Liu, Mingdong Liu, Qi Shao, Dan Wang, Aijun Huang and Cheng He. TIP30 inhibit soligodendrocyte precursor cell differentiation via cytoplasmic sequestration of Olig1. Glia. 2015; 63( 4): 684-98.).

[0050] The result is as figure 2 As shown, under the light microscope, the cell body of Schwann cells is round or oval, with a strong refractive index, and there is an obvious halo around the cell body, and bipolar or tripolar protrusions protrude from the cell body to the surrounding. After 24 hours...

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Abstract

The invention relates to the technical field of cell biology, in particular to a method for separating, purifying and culturing naked mole-rat Schwann cells. The invention comprehensively uses various mediums to separate and purify Schwann cells from the DRG ganglion of the spinal cord of naked mole rat fetal rats, and finds out a reasonable culture method for naked mole rat Schwann cells suitable for temperature-changing rodent mammals. The method of the present invention can obtain a large number of naked mole-rat Schwann cells with normal functional activity in a simple, efficient and economical manner, and the culture under hypoxic conditions can ensure that the biological characteristics of the cells in the in vitro environment can still be maintained. , so that it is convenient to further study the special physiological functions of naked mole rat Schwann cells directly in a pure in vitro cell culture model, thereby providing an important theoretical basis for exploring the biological mechanism and applying it to clinical related fields.

Description

technical field [0001] The invention relates to the technical field of cell biology, in particular to a method for separating, purifying and culturing cells, in particular to a method for separating, purifying and cultivating naked mole-rat Schwann cells. Background technique [0002] Schwann cells (Schwann cells) are myelinating cells of the spinal cord. The myelin sheath structure formed around the axons of neurons provides nutrition, support and protection to neurons, and the existence of myelin sheath can ensure the information between neurons. delivery rate. Immature Schwann cells can be stimulated by the microenvironment to initiate differentiation again. Spinal cord transection injury, amyotrophic lateral sclerosis and other diseases are usually accompanied by myelin damage (Billiards SS, Haynes RL, Folkerth RD, Borenstein NS, Trachtenberg FL, Rowitch DH, Ligon KL, Volpe JJ, KinneyHC.2008. Myelin abnormalities without oligodendrocyte loss in perivascular leukomalaci...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/079
CPCC12N5/0622C12N2500/02C12N2501/135C12N2509/00
Inventor 崔淑芳杨文静倪健孙伟程继帅林丽芳丛薇蔡丽萍余琛琳赵善民徐晨李周桐
Owner SECOND MILITARY MEDICAL UNIV OF THE PEOPLES LIBERATION ARMY
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