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Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Abstract
The intestinal epithelium is the most rapidly self-renewing tissue in adult mammals. We have recently demonstrated the presence of about six cycling Lgr5(+) stem cells at the bottoms of small-intestinal crypts. Here we describe the establishment of long-term culture conditions under which single crypts undergo multiple crypt fission events, while simultanously generating villus-like epithelial domains in which all differentiated cell types are present. Single sorted Lgr5(+) stem cells can also initiate these cryptvillus organoids. Tracing experiments indicate that the Lgr5(+) stem-cell hierarchy is maintained in organoids. We conclude that intestinal cryptvillus units are self-organizing structures, which can be built from a single stem cell in the absence of a non-epithelial cellular niche.
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“Under defined physicochemical conditions, tissues such as small intestine7, colon30,31, stomach32,33, esophagus30, tongue34, liver35–38, lung15, pancreas39–41, heart42, ear43, and skin44 have been obtained from iPSCs, adult or fetal cells, either stem/progenitor cells or differentiated cells.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“adult intestinal stem cells embedded in Matrigel and in the presence of tissue-specific cocktail of growth factors were also shown to self-organize into 3D crypt-villus structures7”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“as this was the first tissue-derived-organoid type established7.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“Organoids can arise either from round colonies generated by single cells7,35 or, from initial multicellular structures such as intestinal crypts30,63, cell aggregates24 or micropatterned cells26.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“This is the reason why intestinal organoids need to be fragmented into smaller cell clusters and reseeded regularly7.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“Intestinal organoids are among the first organoid types successfully established in vitro7,30.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“Most intestinal stem cells could survive, proliferate, and form organoids7.”
From Organoids (2022) · cites this paper as [7]
In the citing paper
“Organoids represent robust in vitro cultures that preserve tissue architecture, stem cell activity, multilineage differentiation, genomic alterations, histology, and pathology of primary tissues1,2.”
From Large-scale CRISPR screening in primary human 3D gastric organoids enables comprehensive dissection of gene-drug interactions (2025) · cites this paper as [1]
In the citing paper
“We further demonstrate the versatility and flexibility of multiplexed CRISPR base-editing for cancer modeling across several epithelial tissues by mutating liver, endometrium, and organoids32–34.”
From One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids (2023) · cites this paper as [34]
In the citing paper
“RhoA signalling might also potentially contribute to cell death, because it can promote apoptosis in low-adhesion environments by increasing cell contractility, explaining why ROCK inhibitors are a standard component of media for stem cells and organoid isolation and maintenance in culture 77-81 .”
From Taxane-induced conformational changes in the microtubule lattice activate GEF-H1-dependent RhoA signalling (2026) · cites this paper as [78]
In the citing paper
“The ability to form organoids depends primarily on ISC function (Barker et al., 2007; Sato et al., 2009).”
From Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells (2017) · cites this paper as Sato et al., 2009
Citations
Cites
Identification of stem cells in small intestine and colon by marker gene Lgr5
Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687
Self-citationGeneralized lacZ expression with the ROSA26 Cre reporter strain
Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
A ROCK inhibitor permits survival of dissociated human embryonic stem cells
Watanabe, K., Ueno, M., Kamiya, D., Nishiyama, A., Matsumura, M., Wataya, T., Takahashi, J. B., Nishikawa, S., Nishikawa, S.-I., Muguruma, K., et al. (2007) · Nature Biotechnology · doi:10.1038/nbt1310 · Cited by 2,055
Cheng, H., & Leblond, C. P. (1974) · American Journal of Anatomy · doi:10.1002/aja.1001410407 · Cited by 1,737
Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4
Kořínek, V., Barker, N., Moerer, P., van Donselaar, E. V., Huls, G., Peters, P., & Clevers, H. (1998) · Nature Genetics · doi:10.1038/1270 · Cited by 1,704
Self-citationvan Es, J. H., van Gijn, M. E., Riccio, O., van den Born, M., Vooijs, M., Begthel, H., Cozijnsen, M., Robine, S., Winton, D. J., Radtke, F., et al. (2005) · Nature · doi:10.1038/nature03659 · Cited by 1,587
Self-citationPurification and unique properties of mammary epithelial stem cells
Stingl, J., Eirew, P. D., Ricketson, I., Shackleton, M. J., Vaillant, F., Choi, D., Li, H. I., & Eaves, C. J. (2006) · Nature · doi:10.1038/nature04496 · Cited by 1,581
Spradling, A. C., Drummond‐Barbosa, D., & Kai, T. (2001) · Nature · doi:10.1038/35102160 · Cited by 1,465
STEM CELL NICHE: Structure and Function
Li, L., & Xie, T. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.012704.131525 · Cited by 1,268
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Ponnurangam, S., Mammen, J. M. V., Ramalingam, S., He, Z., Zhang, Y., Umar, S., Subramaniam, D., & Anant, S. (2012) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-11-0999 · Cited by 107
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Self-citationMileto, S. J., Jardé, T., Childress, K. O., Jensen, J. L., Rogers, A. P., Kerr, G., Hutton, M. L., Sheedlo, M. J., Bloch, S. C., Shupe, J. A., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1915255117 · Cited by 109
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Chiang, H.-Y., Lu, H.-H., Sudhakar, J. N., Chen, Y., Shih, N.-S., Weng, Y.-T., & Shui, J. (2022) · Nature Communications · doi:10.1038/s41467-022-28478-3 · Cited by 107
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Zha, J., Li, H.-S., Lin, Q., Kuo, W., Jiang, Z., Tsai, P.-Y., Ding, N., Jia Rui, W. U., Xu, S.-F., Wang, Y., et al. (2018) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.09.006 · Cited by 113
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Hynds, R. E., & Giangreco, A. (2012) · Stem Cells · doi:10.1002/stem.1290 · Cited by 107
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Gonzalez-Hernandez, M. B., Liu, T., Payne, H. C., Stencel-Baerenwald, J., Ikizler, M. R., Yagita∥, H., Dermody, T. S., Williams, I. R., & Wobus, C. E. (2014) · Journal of Virology · doi:10.1128/jvi.00204-14 · Cited by 105
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Jeffery, V., Goldson, A. J., Dainty, J. R., Chieppa, M., & Sobolewski, A. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1600960 · Cited by 107
Chen, Y., Zhou, W., Roh, T. T., Estes, M. K., & Kaplan, D. L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187880 · Cited by 105
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Langlands, A. J., Almet, A. A., Appleton, P. L., Newton, I. P., Osborne, J. M., & Näthke, I. S. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002491 · Cited by 110
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Reynolds, A. G., Wharton, N., Parris, A., Mitchell, E. M., Sobolewski, A., Kam, C., Bigwood, L., Hadi, A. E., Münsterberg, A., Lewis, M. S., et al. (2013) · Gut · doi:10.1136/gutjnl-2012-304067 · Cited by 111
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Aran, D., Lasry, A., Zinger, A., Biton, M., Pikarsky, E., Hellman, A., Butte, A. J., & Ben‐Neriah, Y. (2016) · Genome biology · doi:10.1186/s13059-016-0995-z · Cited by 104
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Capdevila, C., Miller, J. D., Cheng, L., Kornberg, A. E., George, J. J., Lee, H., Botella, T., Moon, C. S., Murray, J. W., Lam, S., et al. (2024) · Cell · doi:10.1016/j.cell.2024.05.001 · Cited by 106
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Self-citationPowell, R. H., & Behnke, M. S. (2017) · Biology Open · doi:10.1242/bio.021717 · Cited by 103
Chiriac, M. T., Buchen, B., Wandersee, A., Hundorfean, G., Günther, C., Bourjau, Y., Doyle, S. E., Frey, B., Ekici, A. B., Büttner, C., et al. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.03.015 · Cited by 104
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Zheng, H., Wu, D., Wang, S., Li, X. D., Jin, L. N., Zhao, B., Li, S., Sun, Y., Dong, Z., Wu, Q., et al. (2025) · Nature · doi:10.1038/s41586-025-09158-w · Cited by 109
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Stringer, E. J., Duluc, I., Saandi, T., Davidson, I., Bialecka, M., Sato, T., Barker, N., Clevers, H. C., Pritchard, C. A., Winton, D. J., et al. (2011) · Development · doi:10.1242/dev.070722 · Cited by 113
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Zhu, H., Lensch, M. W., Cahan, P., & Daley, G. Q. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2951 · Cited by 104
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Fu, Y., Egorova, A., Sobieski, C., Kuttiyara, J., Calafiore, M., Takashima, S., Clevers, H. C., & Hanash, A. M. (2019) · Immunity · doi:10.1016/j.immuni.2019.06.003 · Cited by 102
Self-citationHeinzelmann, E., Piraino, F., Costa, M., Roch, A., Norkin, M. N., Garnier, V., Homicskó, K., & Brandenberg, N. (2024) · Current Research in Toxicology · doi:10.1016/j.crtox.2024.100197 · Cited by 109
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Yi, J., Bergstrom, K., Fu, J., Shan, X., McDaniel, J. M., McGee, S., Qu, D., Houchen, C. W., Liu, X., & Xia, L. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0237-x · Cited by 103
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Lévy, A., Stedman, A., Deutsch, É., Donnadieu, F., Virgin, H. W., Sansonetti, P. J., & Nigro, G. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902788117 · Cited by 107
Yang, M. H., Darwish, T., Larraufie, P., Rimmington, D., Cimino, I., Goldspink, D. A., Jenkins, B., Koulman, A., Brighton, C. A., Ma, M. K. L., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-81349-7 · Cited by 103
Sakalem, M. E., Síbio, M. T. D., da Costa, F. A. D. S., & de Oliveira, M. (2021) · Biotechnology Journal · doi:10.1002/biot.202000463 · Cited by 112
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Schneeberger, K., Spee, B., Costa, P., Sachs, N., Clevers, H., & Malda, J. (2017) · Biofabrication · doi:10.1088/1758-5090/aa6121 · Cited by 100
Self-citationOlgasi, C., Cucci, A., & Follenzi, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176215 · Cited by 100
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Peng, W. C., de Lau, W., Forneris, F., Granneman, J. C. M., Huch, M., Clevers, H. C., & Gros, P. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.06.009 · Cited by 102
Self-citationde Jong, P. R., Taniguchi, K., Harris, A. R., Bertin, S., Takahashi, N., Duong, J., Campos, A. D., Powis, G., Corr, M., Karin, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11551 · Cited by 100
Puzan, M. L., Hosic, S., Ghio, C., & Koppes, A. N. (2018) · Scientific Reports · doi:10.1038/s41598-018-24768-3 · Cited by 100
Saglam‐Metiner, P., İz, S. G., & Avcı, Ç. B. (2018) · Gene · doi:10.1016/j.gene.2018.11.058 · Cited by 100
Li, L., Fu, F., Guo, S., Wang, H., He, X., Xue, M., Yin, L., Feng, L., & Liu, P. (2018) · Journal of Virology · doi:10.1128/jvi.01682-18 · Cited by 100
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Novellasdemunt, L., Kucharska, A., Jamieson, C., Prange‐Barczynska, M., Baulies, A., Antas, P., van der Vaart, J., Gehart, H., Maurice, M. M., & Li, V. S. W. (2019) · The EMBO Journal · doi:10.15252/embj.2019102771 · Cited by 100
Degree and site of chromosomal instability define its oncogenic potential
Hoevenaar, W. H. M., Janssen, A., Quirindongo, A. I., Ma, H., Klaasen, S. J., Teixeira, A., van Gerwen, B., Lansu, N. R., Morsink, F. H. M., Offerhaus, G. J. A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15279-9 · Cited by 104
Kidney Organoids and Tubuloids
Yengej, F. A. Y., Jansen, J., Rookmaaker, M. B., Verhaar, M. C., & Clevers, H. C. (2020) · Cells · doi:10.3390/cells9061326 · Cited by 107
Self-citationKayisoglu, Ö., Weiß, F., Niklas, C., Pierotti, I., Pompaiah, M., Wallaschek, N., Germer, C., Wiegering, A., & Bartfeld, S. (2020) · Gut · doi:10.1136/gutjnl-2019-319919 · Cited by 100
Human airway cells prevent SARS-CoV-2 multibasic cleavage site cell culture adaptation
Lamers, M. M., Mykytyn, A. Z., Breugem, T. I., Wang, Y., Wu, D. C., Riesebosch, S., van den Doel, P. B., Schipper, D., Bestebroer, T. M., Wu, N. C., et al. (2021) · eLife · doi:10.7554/elife.66815 · Cited by 103
Chiara, G. D., Gervasoni, F., Fakiola, M., Godano, C., D’Oria, C., Azzolin, L., Bonnal, R. J. P., Moreni, G., Drufuca, L., Rossetti, G., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22544-y · Cited by 104
Applications of brain organoids in neurodevelopment and neurological diseases
Sun, N., Meng, X., Liu, Y., Song, D., Jiang, C., & Cai, J. (2021) · Journal of Biomedical Science · doi:10.1186/s12929-021-00728-4 · Cited by 103
The Use of Stem Cell-Derived Organoids in Disease Modeling: An Update
Azar, J. H., Bahmad, H. F., Daher, D., Moubarak, M. M., Hadadeh, O., Monzer, A., Bitar, S. A., Jamal, M., Al‐Sayegh, M., & Abou-Kheir, W. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147667 · Cited by 106
Organoids: a novel modality in disease modeling
Heydari, Z., Moeinvaziri, F., Agarwal, T., Pooyan, P., Shpichka, A. I., Maiti, T. K., Timashev, P. S., Baharvand, H., & Vosough, M. (2021) · Bio-Design and Manufacturing · doi:10.1007/s42242-021-00150-7 · Cited by 106
Intestinal Subepithelial Myofibroblasts Support the Growth of Intestinal Epithelial Stem Cells
Lei, N., Jabaji, Z. B., Wang, J., Joshi, V. S., Brinkley, G. J., Khalil, H. A., Wang, F., Jaroszewicz, A., Pellegrini, M. A., Li, L., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084651 · Cited by 108
Organoids in image-based phenotypic chemical screens
Lukonin, I., Zinner, M., & Liberali, P. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00641-8 · Cited by 99
Patient-derived organoids in translational oncology and drug screening
Yang, R., & Yu, Y. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216180 · Cited by 99
von Furstenberg, R. J., Gulati, A., Baxi, A. C., Doherty, J. M., Stappenbeck, T. S., Gracz, A. D., Magness, S. T., & Henning, S. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00453.2010 · Cited by 104
Functional Genomics of Host–Microbiome Interactions in Humans
Luca, F., Kupfer, S. S., Knights, D., Khoruts, A., & Blekhman, R. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.10.001 · Cited by 103
Development of in vitro enteroids derived from bovine small intestinal crypts
Hamilton, C. A., Young, R. A., Jayaraman, S., Sehgal, A., Paxton, E. A., Thomson, S., Katzer, F., Hope, J. C., Innes, E. A., Morrison, L. J., et al. (2018) · Veterinary Research · doi:10.1186/s13567-018-0547-5 · Cited by 101
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Stine, R. R., Sakers, A. P., TeSlaa, T. A., Kissig, M., Stine, Z. E., Kwon, C. W., Cheng, L., Lim, H., Kaestner, K. H., Rabinowitz, J. D., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.08.017 · Cited by 103
The Past, Present and Future of Intestinal In Vitro Cell Systems for Drug Absorption Studies
Youhanna, S. C., & Lauschke, V. M. (2020) · Journal of Pharmaceutical Sciences · doi:10.1016/j.xphs.2020.07.001 · Cited by 103
Structure and function of non-digestible carbohydrates in the gut microbiome
Rastall, R. A., Díez‐Municio, M., Forssten, S. D., Hamaker, B. R., Meynier, A., Moreno, F. J., Respondek, F., Stahl, B., Venema, K., & Wiese, M. (2022) · Beneficial Microbes · doi:10.3920/bm2021.0090 · Cited by 103
On the biomechanics of stem cell niche formation in the gut – modelling growing organoids
Buske, P., Przybilla, J., Loeffler, M., Sachs, N., Sato, T., Clevers, H. C., & Galle, J. (2012) · FEBS Journal · doi:10.1111/j.1742-4658.2012.08646.x · Cited by 104
Self-citationLee, S. M., Riley, E. M., Meyer, M. B., Benkusky, N. A., Plum, L. A., DeLuca, H. F., & Pike, J. W. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.665794 · Cited by 98
Generation of BAC Transgenic Epithelial Organoids
Schwank, G., Andersson-Rolf, A., Koo, B., Sasaki, N., & Clevers, H. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076871 · Cited by 98
Self-citationLladó, V., Nakanishi, Y., Durán, Á., Reina‐Campos, M., Shelton, P. M., Linares, J. F., Yajima, T., Campos, A. R., Aza‐Blanc, P., Leitges, M., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.01.007 · Cited by 102
Metadata
- Authors
- Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., & Clevers, H.
- Affiliations
- University Medical Center Utrecht (NL)
- The Netherlands Cancer Institute (NL)
- Corresponding author
- Clevers, Hans
- ORCID
- Venue
- Nature
- Published
- 2009-03-29
- Volume
- 459
- Issue
- 7244
- Pages
- 262-265
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1965157206
- Cited by
- 7,204
- References
- 33
- Citations by year
- 2026: 537 · 2025: 663 · 2024: 658 · 2023: 663 · 2022: 640 · 2021: 680 · 2020: 636 · 2019: 433 · 2018: 450 · 2017: 397 · 2016: 341 · 2015: 260 · 2014: 223 · 2013: 204 · 2012: 159
- FWCI
- 69.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (submittedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Health Sciences › Medicine › Gastroenterology › Digestive system and related health
- Keywords
- Lgr5, intestinal stem cells, intestinal crypts, self-organizing structures, mesenchymal niche, intestinal epithelium, stem cell hierarchy, crypt fission, cell tracing
- MeSH terms
- Animals, Cell Separation, Intestinal Mucosa, Intestines, Mesoderm, Organoids, Regeneration, Stem Cells, Gene Expression Regulation, Developmental, Cell Culture Techniques, Cell Lineage, Paneth Cells, Multipotent Stem Cells, Receptors, G-Protein-Coupled, Mice, Receptors, Notch, Stem Cell Niche
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