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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here, we established a low cost and easy to operate method that directs fast and efficient differentiation from embryonic stem cells into neurons. This method is suitable for popularization among laboratories and can be a useful tool for neurological research.

Abstract

The neural differentiation of mouse embryonic stem cells (mESCs) is a potential tool for elucidating the key mechanisms involved in neurogenesis and potentially aid in regenerative medicine. Here, we established an efficient and low cost method for neuronal differentiation from mESCs in vitro, using the strategy of combinatorial screening. Under the conditions defined here, the 2-day embryoid body formation + 6-day retinoic acid induction protocol permits fast and efficient differentiation from mESCs into neural precursor cells (NPCs), as seen by the formation of well-stacked and neurite-like A2lox and 129 derivatives that are Nestin positive. The healthy state of embryoid bodies and the timepoint at which retinoic acid (RA) is applied, as well as the RA concentrations, are critical in the process. In the subsequent differentiation from NPCs into neurons, N2B27 medium II (supplemented by Neurobasal medium) could better support the long term maintenance and maturation of neuronal cells. The presented method is highly efficiency, low cost and easy to operate, and can be a powerful tool for neurobiology and developmental biology research.

Introduction

Embryonic stem cells (ESCs) are pluripotent and can differentiate into neural precursor cells (NPCs) and subsequently into neurons under certain conditions1. ESC-based neurogenesis provides the best platform to mimic neurogenesis, thus serving as a useful tool for developmental biology studies and potentially aid in regenerative medicine2,3. In the past decades, many strategies have been reported for inducing embryonic neurogenesis, such as the transgenic method4, using small molecules5, using a 3D matrix microenvironment

Protocol

1. Mouse embryonic stem cell culture

  1. Prepare 0.1% gelatin coated cell culture dishes or plates.
    1. Add 2 mL of sterilized 0.1% gelatin (0.1% w/v in water) to 60 mm cell culture dishes. Rock gently to ensure even coating of the cell culture dishes.
    2. Put the dishes into a 5% CO2 incubator at 37 °C and allow coating for 1 h.
    3. Remove the 0.1% gelatin solution before seeding the cells.
      NOTE: After removing the gelatin, there is no need to dry or wash the coated .......

Representative Results

2-day embryoid body formation + 6-day RA induction works best on directing the differentiation of mESCs into NPCs (Phase I). To determine the optimal protocol that best promote the differentiation of mESCs into NPCs (Phase I), 7 protocols were tested on both A2lox and 129 mESCs (Table 1) and the differentiation status of each group was monitored using light microscope. As shown in Figure 3A, most A2lox and 129 derivatives under "2-day embryoid body formation + 6-day RA i.......

Discussion

In the present study, we established a simple and effective method for neuronal differentiation from mESCs, with low cost and easily obtained materials. In this method, 2 days of embryoid body formation followed by 6 days of RA induction can effectively promote the differentiation of mESCs into NPCs (Phase I-protocol 3). For the phase II differentiation, N2B27 medium II (Phase II-protocol 3) most effectively induce the differentiation from NPCs into neurons. To ensure success, more attention should be paid to several cri.......

Acknowledgements

This work was supported by the National Natural Science Foundation of China (No. 31501099) and the Middle-aged and Young of the Education Department of Hubei Province, China (No. Q20191104). And, we thank Professor Wensheng Deng at Wuhan University of Science and Technology for providing the mouse embryonic stem cell lines A2lox.

....

Materials

NameCompanyCatalog NumberComments
Anti-Nestin antibody [Rat-401]AbcamAb11306stored at -80 °C, avoid repeated freezing and thawing
Anti-β-Tubulin III antibody produced in rabbitSigma AldrichT2200stored at -80 °C, avoid repeated freezing and thawing
Alexa Fluor 488-Labeled Goat Anti-Mouse IgGBeyotimeA0428stored at -20 °C and protect from light
B-27 Supplement (50X), serum freeGibco17504044stored at -20 °C, and protect from light
CHIR-99021 (CT99021)SelleckS1263stored at -20 °C
CoverslipsNEST801007
Cy3-Labeled Goat Anti-Rabbit IgGBeyotimeA0516stored at -20 °C and protect from light
DME/F-12 1:1 (1x)HyCloneSH30023.01Bstored at 4 °C
Fetal bovine serumHyCloneSH30084.03stored at -20 °C, avoid repeated freezing and thawing
Fluorescence microscopyOlympusCKX53
GelatinGibcoCM0635Bstored at room temperature
GlutaMAX SupplementGibco35050061stored at 4 °C
Immunol Staining Primary Antibody dilution BufferBeyotimeP0103stored at 4 °C
KnockOut DMEM/F-12Gibco12660012stored at 4 °C
KnockOut Serum ReplacementGibco10828028stored at -20 °C, avoid repeated freezing and thawing
Leukemia Inhibitory Factor humanSigmaL5283stored at -20 °C
Mounting Medium With DAPI - Aqueous, FluoroshieldAbcamab104139stored at 4 °C and protect from light
MEM Non-essential amino acids solutionGibco11140076stored at 4 °C
N-2 Supplement (100X)Gibco17502048stored at -20 °C and protect from light
Normal goat serumJackson005-000-121stored at -20 °C
Neurobasal MediumGibco21103049stored at 4 °C
Nonadhesive bacterial dishCorning3262
Phosphate Buffered Saline (1X)HyCloneSH30256.01Bstored at 4 °C
Penicillin/ Streptomycin SolutionHyCloneSV30010stored at 4 °C
PD0325901(Mirdametinib)SelleckS1036stored at -20 °C
Retinoic acidSigmaR2625stored at -80 °C and protect from light
Strain 129 Mouse Embryonic Stem CellsCyagenMUAES-01001Maintained in feeder-free culture system
Stem-Cellbanker (DMSO free)ZENOAQstem cellbanker DMSO freestored at -20 °C, avoid repeated freezing and thawing
Trypsin 0.25% (1X) SolutionHyCloneSH30042.01stored at 4 °C
Triton X-100SigmaT8787
2-MercaptoethanolGibco21985023stored at 4 °C and protect from light
4% paraformaldehydeBeyotimeP0098stored at -20 °C
6 - well plateCorning3516
60 mm cell culture dishCorning430166
15 ml centrifuge tubeNUNC339650

References

  1. Vieira, M. S., et al. Neural stem cell differentiation into mature neurons: mechanisms of regulation and biotechnological applications. Biotechnology Advances. 36 (7), 1946-1970 (2018).
  2. Yang, J. R., Lin, Y. T., Liao, C. H.

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Neuronal DifferentiationMouse Embryonic Stem CellsIn VitroEmbryoid Body FormationRetinoic Acid InductionNeurogenesisNeural LineageStem Cell Differentiation

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