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Series GSE235892 Query DataSets for GSE235892
Status Public on Jun 28, 2024
Title Global gene expression profiling of organoids with various morphologies generated in cerebral organoid differentiation
Organism Homo sapiens
Experiment type Expression profiling by array
Summary To characterize organoids with each type of morphology, we performed DNA microarray analysis to identify genes expressed predominantly in each type of organoids on day35 of cortical organoid differentiation protocol (SFBEq).
 
Overall design To generate cortical organoids, we employed the differentiation method previously described by Kitahara et al., Stem Cell Reports, 2020. Human induced pluripotent stem cells are cultured in DMEM/F-12 GlutaMAX supplemented with 20% (v/v) KnockOut Serum Replacement (KSR), 5 µM SB431542, and 3 µM IWR1e, using low adheshion 96 well plates.Defining the day on which floating culture of cell aggregates was started as day0, half the medium was changed once every three days until day 15. On day 18, the aggregated cells were transferred to 90-mm non-coated dishes and further cultured in DMEM/F-12 GlutaMAX supplemented with 1% (v/v) N-2 Supplement, 1% (v/v) Chemically Defined Lipid Concentrate (CDLC), 0.25 µg/ml Amphotericin B , 100 U/ml penicillin, and 100 µg/ml streptomycin until day 35. Organoids were cultured on an orbital shaker and maintained at 50 rpm in 20% O2 and 5% CO2 to eliminate the need for cell culture in 40% O2. Complete medium changes were performed once every 3 or 4 days from day 18 to day 35. On day35, partial structures in organoids were classified into 7 groups according to their morphologies. (1) Rosettes, organoids with rosette structures throughout; (2) Potato-like”, those with low transparency and no clear internal structures; (3) Balloon-like, those with balloon-like cystic structures; (4) Cotton-like, organoids with fibrous epithelial-like structures; (5) Transparent, transparent organoids and cyst-like internal structures; (6) Jelly-like, organoids with a transparent periphery and no clear internal structures; and (7) Pigmented, organoids with pigmentation.The tissues with distinct morphological features were isolated by dissection and subjected to microarray analysis. For each morphological groups, 3 samples are analyzed.
 
Contributor(s) Ikeda M, Takahashi J
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Submission date Jun 27, 2023
Last update date Jun 28, 2024
Contact name Megumi Ikeda
E-mail(s) [email protected]
Phone 08053578355
Organization name Center for iPS Cell Research and Application, Kyoto University
Department Department of Clinical Application
Street address 53 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, JAPAN
City Kyoto
ZIP/Postal code 6068507
Country Japan
 
Platforms (1)
GPL570 [HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
Samples (21)
GSM7511557 Rosette structures, biological rep1
GSM7511558 Rosette structures, biological rep2
GSM7511559 Rosette structures, biological rep3
Relations
BioProject PRJNA987994

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE235892_GCD042_220711_RMA_with_base_line_filtered.txt.gz 18.7 Mb (ftp)(http) TXT
GSE235892_RAW.tar 97.0 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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