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In This Article

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

Summary

The protocol combines human intestinal organoid technology with single cell transcriptomic analysis to provide significant insight into previously unexplored intestinal biology.

Abstract

Single cell transcriptomics has revolutionized our understanding of the cell biology of the human body. State-of-the-art human small intestinal organoid cultures provide ex vivo model systems that bridge the gap between animal models and clinical studies. The application of single cell transcriptomics to human intestinal organoid (HIO) models is revealing previously unrecognized cell biology, biochemistry, and physiology of the GI tract. The advanced single cell transcriptomics platforms use microfluidic partitioning and barcoding to generate cDNA libraries. These barcoded cDNAs can be easily sequenced by next generation sequencing platforms and used by various visualization tools to generate maps. Here, we describe methods to culture and differentiate human small intestinal HIOs in different formats and procedures for isolating viable cells from these formats that are suitable for use in single-cell transcriptional profiling platforms. These protocols and procedures facilitate the use of small intestinal HIOs to obtain an increased understanding of the cellular response of human intestinal epithelium at the transcriptional level in the context of a variety of different environments.

Introduction

The small intestinal epithelium has two distinct zones: the crypt that houses the intestinal stem cell (ISC) and the villus, which is comprised of differentiated cells of the secretory and absorptive lineages. Adding to this complexity is the regional specificity of the epithelium that provides unique functional properties between the regions of the small intestine. Pioneering work established culture conditions in which both the human small intestinal crypt and villus zones can be generated ex vivo from surgical tissues or tissue biopsies1. These cultures are bridging the gap between animal studies and clinical trials and are revealin....

Protocol

The organoid lines used here were obtained from the Texas Medical Center Digestive Disease Center GEMS Core. Briefly, to initially establish organoid lines, donor tissue samples were washed and enzymatically digested to release the intestinal crypts. Crypts were embedded in a basement membrane and cultured in a medium. The Institutional Review Board at Baylor College of Medicine approved the study protocol to obtain tissue samples from which organoid lines were established, and informed consent was obtained from all dono.......

Representative Results

Single-cell suspensions were pooled from 2-3 wells of membrane cell culture insert, monolayer, and 3D HIOs to ensure sufficient cell yield and reduce well-to-well variation. Single cell libraries were prepared using reagents specific to the single cell transcriptional profiling platform. and sequenced with paired end reads on a next generation sequencing platform, 30,000 reads/cell. Reads were mapped, counted, and analyzed using analytical tools for single cell genomics. Low-quality cells with more than 20% mitochondrial.......

Discussion

Using single cell genomics platforms, complex biological systems, such as tissue derived HIO cultures that model the intestinal epithelium, can be broken down to yield individual cellular contributions to overall biological response4,5,6. Cellular heterogeneity and rare cell populations can also be identified and interrogated. Cellular input needs to be optimized to maximize output using single cell transcriptomic-based platform.......

Acknowledgements

The authors acknowledge U19 AI157984, U01 DK103168, U19 AI144297, P30 DK56338, P01 AI057788, U19 AI116497 grants and NASA Cooperative Agreement Notice/TRISH NNX16AO69A.

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Materials

NameCompanyCatalog NumberComments
[Leu15]-Gastrin ISigma-AldrichG914510 nM
0.05% Trypsin-EDTAInvitrogen25300054
0.4% Trypan blueMillipore-SigmaT8154
0.5 M EDTACorning46-034-CI
1x PBS Ca- Mg-Corning21-040-CM
24 mm TranswellCostar3412
24 well Nunclon delta surface tissue culture dishThermo Scientific142475
40 µm cell strainerFalcon352340
40 µm Flowmi tip strainerSP Bel-Art LabwareH13680-0040
70 µm Flowmi tip strainerSP Bel-Art LabwareH13680-0070
96 well plateCorning3595
A-83-01Tocris2939500 nM
AccutaseStemCell Technologies7920
Advanced DMEM/F12Invitrogen12634-028
B27 supplementInvitrogen17504-0441X
Chromium Next GEM Single Cell 3’ GEM, Library & Gel Bead Kit v3.110x GenomicsPN-1000128
Collagen IVSigma-AldrichC5533-5MG33 µg/mL
Corning Cell Recovery Solution VWR354253
DPBS (Mg2-, Ca2-)Invitrogen14190-1361X
GlutaMAX-IInvitrogen35050-0612 mM
HEPES 1MInvitrogen15630-08010 mM
L-WRN conditioned mediaATCCCRL-3276
Matrigel, GFR, phenol freeCorning356231
mouse recombinant EGFInvitrogenPMG804350 ng/mL
N2 supplementInvitrogen17502-0481X
N-AcetylcysteineSigma-AldrichA9165-5G500 µM
NicotinamideSigma-AldrichN063610 mM
SB202190Sigma-AldrichS706710 µM
TranswellCorning3413
Y27632Stem Cell Technologies7230810 µM

References

  1. Sato, T., et al. Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. Gastroenterology. 141 (5), 1762-1772 (2011).
  2. Blutt, S. E., et al. G....

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Intestinal OrganoidsSingle cell TranscriptomicsHuman Small IntestineEpitheliumCell BiologyMicrofluidicsNext generation SequencingCell IsolationCell Differentiation

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