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SRX15372279: GSM6170832: IBD-drop-d7, replicate 1, scRNAseq; Homo sapiens; RNA-Seq
2 ILLUMINA (Illumina NovaSeq 6000) runs: 349.4M spots, 44.4G bases, 13.7Gb downloads

External Id: GSM6170832_r1
Submitted by: University of Pennsylvania
Study: Geometric engineering of organoid culture for enhanced organogenesis in a dish
show Abstracthide Abstract
Here we introduce a facile, scalable engineering approach to enable long-term development and maturation of organoids. We have redesigned the configuration of conventional organoid culture to develop a platform that converts single injections of stem cell suspensions to radial arrays of organoids that can be maintained for extended periods without the need for passaging. Using this system, we demonstrate accelerated production of intestinal organoids with significantly enhanced structural and functional maturity, and their continuous development for over 4 weeks. Furthermore, we present a patient-derived organoid model of inflammatory bowel disease (IBD) and its interrogation using single-cell RNA sequencing to demonstrate its ability to reproduce key pathological features of IBD. Finally, we describe the extension of our approach to engineer vascularized, perfusable human enteroids, which can be used to model innate immune responses in IBD. This work provides an immediately deployable platform technology towards engineering more realistic organ-like structures in a dish. Overall design: Intestinal epithelial cells isolated from enteroids of the control and IBD patients were analyzed using scRNAseq.
Sample: IBD-drop-d7, replicate 1, scRNAseq
SAMN28548424 • SRS13101181 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM6170832
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Enteroid lines are generated from terminal ileum mucosal biopsies. Briefly, two biopsy tissue fragments were rinsed 3 times in 1 ml cold sterile PBS, then incubated in cold chelation buffer for 30 minutes on a turntable in a cold room, followed by mechanical dis-sociation (scraping) of epithelial layer. The fragments were strained through a 100 μm strainer to deplete the villi and resuspended in 80% Matrigel, then seeded at the density of 50-200 crypts per 30 μl drop. The droplets solidified at 37ºC for 30 minutes, and 500 μl human IntestiCult (STEMCELL Technologies; complete when supplemented with Penicillin-Streptomycin (Gibco)) was added per well. Y-27632 (SelleckChem; final conc. 10 μM) was added to culture medium at seeding only. Single-cell suspension for each organoid sample was loaded onto a separate channel of a Chromium 10X Genomics Single Cell 3' Reagent Kit v2 library chip (10X Genomics) according to the manufacturer's protocol. RNA transcripts from single cells were uniquely barcoded and reverse-transcribed. cDNA sequencing libraries were prepared according to the manufacturer's protocol (10X user guide for library prep) and sequenced on an Illumina NovaSeq 6000 using an S1 100 cycles flow cell v1.5. Library quality control was done using Agilent TapeStation for sizing (bp) and KAPA qPCR for concentration (nM).
Runs: 2 runs, 349.4M spots, 44.4G bases, 13.7Gb
Run# of Spots# of BasesSizePublished
SRR19312102174,554,35022.2G6.8Gb2023-01-12
SRR19312103174,845,32722.2G6.9Gb2023-01-12

ID:
21910674

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