Efficient induction of definitive endoderm from pluripotent stem cells
a technology of endoderm and pluripotent stem cells, which is applied in the direction of artificial cell constructs, drug compositions, metabolic disorders, etc., can solve the problems of insufficient development of reliable protocols for generating fully functional beta cells, inability to efficiently and robustly control the effect of the endoderm, and inability to efficiently and robustly control the effect of endoderm
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example 1
In Vitro Culture of Human ES / iPS Cells
[0239]The DE protocol was confirmed in two different feeder free (DEF, mTeSR) culture systems and one feeder dependent (MEF-ES) culture system.
[0240]DEF hESC / iPS Culture System
[0241]Human embryonic stem (hES) cells SA121 and chIPS4 (Cellartis) were grown on human fibronectin (Sigma) in DEF culture media (Cellartis) with 30 ng / ml bFGF (Invitrogen) and 10 ng / ml Noggin (Peprotech) in 6-96 well plates. Cells were single cell passaged with Rock inhibitor Y-27632 (Calbiochem) and seeded at a density of 40000 cells / cm2 for experiments. Experiments were initiated 4 d after passage.
[0242]mTeSR Culture System
[0243]hES cells (SA121) were cluster passaged from feeders (MEFs) to Matrigel (BD Biosciences) in mTeSR1 media (Cell Signaling Technologies) and passaged further with Dispase (BD Biosciences) according to the culture system protocol. DE was initiated once clusters started to touch each other
[0244]MEF-ES
[0245]hES cells (SA121) were passaged on gelatine...
example 2
CHIR DE Protocol
[0246]Confluent cultures were washed once in RPMI1640 (Invitrogen) before 24 hour pre-treatment with 0.5-7 μM CHIR99021 (Stemgent) in RPMI. Control cells were left untreated in RPMI and D'Amour cells were either left in RPMI or treated with AA (Peprotech)+Wnt3a (R&D Systems) without pre-treatment depending on experimental setup.
[0247]After 24 hours, pretreated and control cells were washed once with RPMI before adding 100 ng / ml AA in RPMI. D'Amour cells were also treated with 100 ng / ml AA but with 0.2% FBS instead of B27. 24 h later, 2% B27 (Invitrogen) was added to the AA media for 2-3 d. Control cells were treated with B27 to prevent cell death and D'Amour cells with 2% FBS according to published protocol. Media was changed every day.
[0248]When cells were further differentiated to PE, the DE protocol was applied in T75 cell culture flasks and reseeded after 4 d of DE culture at a density of 200K in DE media. 1 d later, cells were washed once before addition of PE m...
example 3
RNA Extraction and Quantitative Real-Time PCR
[0258]RNA samples were collected after 24 h pre-treatment (D1), after 1 day of AA treatment (D2) and after 1-2 d of AA+B27 treatment (D3-4). Total RNA was extracted with the Rneasy Plus Mini kit (Qiagen) and quantitative real-time PCR was performed using the StepOnePLus system (Applied Biosystems).
[0259]ICC Staining Procedure
[0260]Cells were washed in PBS+ / + and fixed in 4% formaldehyde for 30 min (10% formaline, VWR). The cells were then washed again three times in PBS and left in PBS (4° C.) until staining. Fixed cells were washed with PBS once, then permeabilized with 0.5% Triton X-100 in PBS for 6 min, washed in PBS and blocked with TNB buffer (0.1M Tris-HCL pH 7.5, 0.15M NaCl, 0.5% Blocking Reagent (Perkin Elmer)) for 30 min. Primary antibodies (goat-antiSOX17 (AF1924, RnD Systems); goat-anti-Brachyury (AF2085, RnD Systems); mouse-antiOCT4 (sc5279, SantaCruz Biotechnology); goat-anti-PDX1 (AB47383, Abcam)) were added in 0.1% TritonX-...
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