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  • Improvement of Cell Survival During Human Pluripotent Stem Cell Definitive Endoderm Differentiation.

Improvement of Cell Survival During Human Pluripotent Stem Cell Definitive Endoderm Differentiation.

Stem cells and development (2015-07-02)
Han Wang, Xie Luo, Li Yao, Donna M Lehman, Pei Wang
ZUSAMMENFASSUNG

Definitive endoderm (DE) is a vital precursor for internal organs such as liver and pancreas. Efficient protocol to differentiate human embryonic stem cells (hESCs) or induced pluripotent stem cells (iPSCs) to DE is essential for regenerative medicine and for modeling diseases; yet, poor cell survival during DE differentiation remains unsolved. In this study, our use of B27 supplement in modified differentiation protocols has led to a substantial improvement. We used an SOX17-enhanced green fluorescent protein (eGFP) reporter hESC line to compare and modify established DE differentiation protocols. Both total live cell numbers and the percentages of eGFP-positive cells were used to assess differentiation efficiency. Among tested protocols, three modified protocols with serum-free B27 supplement were developed to generate a high number of DE cells. Massive cell death was avoided during DE differentiation and the percentage of DE cells remained high. When the resulting DE cells were further differentiated toward the pancreatic lineage, the expression of pancreatic-specific markers was significantly increased. Similar high DE differentiation efficiency was observed in H1 hESCs and iPSCs through the modified protocols. In B27 components, bovine serum albumin was found to facilitate DE differentiation and cell survival. Using our modified DE differentiation protocols, satisfactory quantities of quality DE can be produced as primary material for further endoderm lineage differentiation.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
RPMI-1640-Medium, With L-glutamine and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture
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Penicillin-Streptomycin, Solution stabilized, with 10,000 units penicillin and 10 mg streptomycin/mL, 0.1 μm filtered, BioReagent, suitable for cell culture
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2-Mercaptoethanol, Molecular Biology, suitable for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration)
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2-Mercaptoethanol, ≥99.0%
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DAPI, for nucleic acid staining
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L-Glutamin, meets USP testing specifications, suitable for cell culture, 99.0-101.0%, from non-animal source
Millipore
Accutase Zellablösungslösung, A cell detachment solution of proteolytic & collagenolytic enzymes. The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue.
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L-Glutamin, ReagentPlus®, ≥99% (HPLC)
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2-Mercaptoethanol, BioUltra, Molecular Biology, ≥99.0% (GC)
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Natriumbutyrat, 98%
SAFC
L-Glutamin
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Natriumbutyrat, ≥98.5% (GC)
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L-Glutamin, BioUltra, ≥99.5% (NT)
Supelco
Retinol -Lösung, 100 μg/mL ± 25% (Refer to COA) (Ethanol with 0.1% (w/v) BHT), ampule of 1 mL, reference material, Cerilliant®
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L-Glutamin, γ-irradiated, BioXtra, suitable for cell culture
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L-Glutamin
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FGF-2 human, recombinant, expressed in insect cells, ≥85% (SDS-PAGE)