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In This Article

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

Summary

Hepatocytes derived from pluripotent stem cells can be purified through cell sorting, using a combination of mitochondrial and activated leukocyte cell adhesion molecule (ALCAM, also known as CD166) staining.

Abstract

Human embryonic stem (ES) and induced pluripotent stem (iPS) cells have potential applications in cell-based regenerative medicine for treating severely diseased organs due to their unlimited proliferation and pluripotent properties. However, differentiating human ES/iPS cells into 100% pure target cell types is challenging due to their high sensitivity to the environment. Tumorigenesis after transplantation is caused by contaminated, proliferating, and undifferentiated cells, making high-purification technology essential for the safe realization of regenerative medicine. To mitigate the risk of tumorigenesis, a high-purification technology has been developed for human iPS cell-derived hepatocytes. The method employs FACS (fluorescence-activated cell sorting) using a combination of high mitochondrial content and the cell-surface marker ALCAM (activated leukocyte cell adhesion molecule) without genetic modification. 97% ± 0.38% (n = 5) of the purified hepatocytes using this method exhibited albumin protein expression. This article aims to provide detailed procedures for this method, as applied to the most current two-dimensional differentiation method for human iPS cells into hepatocytes.

Introduction

Embryonic and induced pluripotent stem cells (ES and iPS, respectively) are considered promising cell sources for regenerative therapies. However, the efficiency of differentiating these cells into specific target cell types can vary, even when using the same cell line, protocol, and experimenter1,2,3,4. This variability may be attributed to the high sensitivity of human ES/iPS cells to their environment. Therefore, it is currently difficult to consistently obtain pure target cells. To achieve highly safe regenerative medicine, it is crucial....

Protocol

This study used commercially obtained human iPS cells (253G1 strain) (see Table of Materials).

1. Maintenance of human iPS cells

  1. Maintain human iPS cells in feeder-free conditions in AK02 medium on culture dishes coated with 0.25 µg/cm2 iMatrix-511 (see Table of Materials).

2. Hepatic differentiation of human iPS cells in 2D cultures

NOTE:.......

Representative Results

The timeline of the processes inducing human iPS cells to differentiate into hepatocytes through 2D culture (Figure 1A) and representative cell features (Figure 1B) are shown. Approximately on differentiation day 12, cells began to exhibit polygonal cell shapes and round nuclei, characteristic of hepatocytes. Some hepatocytes also displayed multinucleation.

FACS analysis was performed using the cells on differentiation day 27. To iden.......

Discussion

Due to their functions in nutrient metabolism and detoxification, hepatocytes possess a relatively large number of mitochondria compared to other cell types15. ALCAM is a member of the immunoglobulin superfamily and plays a role in cell adhesion and migration. It is expressed in various cell types, including hepatic, epithelial, lymphocytic, myeloid, fibroblast, and neuronal cells16. By utilizing a combination of the mitochondria-based method and the ALCAM antibody, human i.......

Acknowledgements

This work was supported by the Ministry of Education, Culture, Sports, Science and Technology grant number [23390072].

....

Materials

NameCompanyCatalog NumberComments
253G1 human iPS cell lineRIKEN BioResource Research CenterHPS0002
4% paraformaldehydeFUJIFILM Wako Pure Chemical Corporation163-20145
Activin A Solution, Human, RecombinantNACALAI TESQUE, INC.18585
Anti-Nuclei Antibody, clone 235-1ChemiconMAB1281Antibody against human nuclear antigen
B-27 Supplement (50x), serum freeThermo Fisher Scientific17504044
BD FACSAria IIIBD BiosciencesCell sorter
CHIR-99021MedChemExpressHY-10182 
Ciclosporin AFUJIFILM Wako Pure Chemical Corporation035-18961
CollagenaseFUJIFILM Wako Pure Chemical Corporation034-22363
Corning Matrigel Growth Factor Reduced (GFR) Basement Membrane MatrixCorning354230Gel-like basement membrane matrix
CultureSure Y-27632FUJIFILM Wako Pure Chemical Corporation036-24023ROCK inhibitor
DexamethasoneFUJIFILM Wako Pure Chemical Corporation047-18863
Dimethyl sulfoxide (DMSO)FUJIFILM Wako Pure Chemical Corporation047-29353
Donkey anti-Goat IgG (H+L) Cross-Adsorbed Secondary Antibody, Alexa Fluor 488Thermo Fisher ScientificA-11055
Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 546Thermo Fisher ScientificA10036
Donkey anti-Rabbit IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 488Thermo Fisher ScientificA-21206
Falcon 5 mL Round Bottom Polystyrene Test Tube, with Cell Strainer Snap CapCorning352235
Fetal Bovine SerumBiowest51820-500
GlutaMAX SupplementThermo Fisher Scientific35050061Dipeptide L-Alanyl-L-Glutamine
Human/Mouse/Rat/Canine ALCAM/CD166 AntibodyR&D SystemsAF1172
Hydrocortisone 21-hemisuccinate sodium saltSigma-AldrichH2270
iMatrix-511 silkNippi892021
ImmunoBlockKACCTKN001Blocking solution
ITS-G Supplement(×100)FUJIFILM Wako Pure Chemical Corporation090-06741
Leibovitz's L-15 MediumFUJIFILM Wako Pure Chemical Corporation128-06075
N-Hexanoic-Try-Ile-(6)-amino Hexanoic amide (Dihexa)Toronto Research ChemicalsH293745
Polyclonal Rabbit Anti-Human AlbuminDakoA0001
Polyoxyethylene Sorbitan Monolaurate (Tween 20)NACALAI TESQUE, INC.28353-85
RPMI-1640FUJIFILM Wako Pure Chemical Corporation189-02025
Sodium L-AscorbateNACALAI TESQUE, INC.03422-32
StemFit AK02NREPROCELLRCAK02N
TBS (10x)NACALAI TESQUE, INC.12748-31
Tetramethylrhodamine, methyl ester (TMRM)Thermo Fisher ScientificT668
Triton X-100NACALAI TESQUE, INC.28229-25
Trypan Blue SolutionNACALAI TESQUE, INC.20577-34
TRYPSIN 250Difco215240
Tryptose phosphate broth solutionSigma-AldrichT8159

References

  1. Yamamoto, T., et al. Differentiation potential of pluripotent stem cells correlates to the level of CHD7. Scientific Reports. 8 (1), 241 (2018).
  2. Laco, F., et al.

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