The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.
Redundant Sources of Wnt Regulate Intestinal Stem Cells and Promote Formation of Paneth Cells
Open accessAbstract
Background & aims Wnt signaling regulates multiple aspects of intestinal physiology, including stem cell maintenance. Paneth cells support stem cells by secreting Wnt, but little is known about the exact sources and primary functions of individual Wnt family members.Methods We analyzed intestinal tissues and cultured epithelial cells from adult mice with conditional deletion of Wnt3 (Vil-CreERT2;Wnt3fl/fl mice). We also analyzed intestinal tissues and cells from Atoh1 mutant mice, which lack secretory cells.Results Unexpectedly, Wnt3 was dispensable for maintenance of intestinal stem cells in mice, indicating a redundancy of Wnt signals. By contrast, cultured crypt organoids required Paneth cell-derived Wnt3. Addition of exogenous Wnt, or coculture with mesenchymal cells, restored growth of Vil-CreERT2;Wnt3fl/fl crypt organoids. Intestinal organoids from Atoh1 mutant mice did not grow or form Paneth cells; addition of Wnt3 allowed growth in the absence of Paneth cells. Wnt signaling had a synergistic effect with the Lgr4/5 ligand R-spondin to induce formation of Paneth cells. Mosaic expression of Wnt3 in organoids using a retroviral vector promoted differentiation of Paneth cells in a cell-autonomous manner.Conclusions Wnt is part of a signaling loop that affects homeostasis of intestinal stem and Paneth cells in mice. Wnt3 signaling is required for growth and development of organoid cultures, whereas nonepithelial Wnt signals could provide a secondary physiological source of Wnt.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Quantitative real-time RT-PCR analyses for expression of Wnt1, 2, 2b, 3, 3a, 8a, 8b, 10a, and 10b (Farin et al., 2012) in ISCs demonstrated reduced Wnt3 (Figure 3C) levels in aged ISCs.”
From Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells (2017) · cites this paper as Farin et al., 2012
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
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., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204
Self-citationIdentification 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
Sato, T., Stange, D. E., Ferrante, M., Vries, R. G. J., van Es, J. H., van den Brink, S., van Houdt, W. J., Pronk, A., van Gorp, J., Siersema, P. D., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.050 · Cited by 3,753
Self-citationPaneth cells constitute the niche for Lgr5 stem cells in intestinal crypts
Sato, T., van Es, J. H., Snippert, H. J., Stange, D. E., Vries, R. G., van den Born, M., Barker, N., Shroyer, N. F., van de Wetering, M., & Clevers, H. (2011) · Nature · doi:10.1038/nature09637 · Cited by 2,510
Self-citationThe β-Catenin/TCF-4 Complex Imposes a Crypt Progenitor Phenotype on Colorectal Cancer Cells
van de Wetering, M., Sancho, E., Verweij, C., de Lau, W., Oving, I., Hurlstone, A., van der Horn, K., Batlle, E., Coudreuse, D., Haramis, A.-P., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01014-0 · Cited by 2,030
Self-citationStem Cells, Self-Renewal, and Differentiation in the Intestinal Epithelium
van der Flier, L. G., & Clevers, H. C. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163145 · Cited by 1,994
Self-citationDepletion 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-citationLgr5 homologues associate with Wnt receptors and mediate R-spondin signalling
de Lau, W., Barker, N., Low, T. Y., Koo, B., Li, V. S. W., Teunissen, H., Kujala, P., Haegebarth, A., Peters, P. J., van de Wetering, M., et al. (2011) · Nature · doi:10.1038/nature10337 · Cited by 1,302
Self-citationBmi1 is expressed in vivo in intestinal stem cells
Sangiorgi, E., & Capecchi, M. R. (2008) · Nature Genetics · doi:10.1038/ng.165 · Cited by 1,245
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 656
Intestinal stromal cells in mucosal immunity and homeostasis
Owens, B. M. J., & Simmons, A. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.125 · Cited by 117
Intestinal Stem Cells and Their Defining Niche
Tan, D. W., & Barker, N. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00003-2 · Cited by 119
The regulatory niche of intestinal stem cells
Sailaja, B. S., He, X., & Li, L. (2016) · The Journal of Physiology · doi:10.1113/jp271931 · Cited by 121
Ex vivo culture of the intestinal epithelium: strategies and applications
Leushacke, M., & Barker, N. (2014) · Gut · doi:10.1136/gutjnl-2014-307204 · Cited by 117
Yu, M. S., Qin, K. H., Fan, J., Zhao, G., Zhao, P., Zeng, W., Chen, C., Wang, A., Wang, Y., Zhong, J., et al. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2023.04.042 · Cited by 125
Brügger, M. D., Valenta, T., Fazilaty, H., Hausmann, G., & Basler, K. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3001032 · Cited by 107
Kraiczy, J., McCarthy, N., Malagola, E., Tie, G., Madha, S., Boffelli, D., Wagner, D. E., Wang, T. C., & Shivdasani, R. A. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.03.004 · Cited by 112
Fafílek, B., Krausová, M., Vojtěchová, M., Pospíchalová, V., Tůmová, L., Šloncová, E., Huranová, M., Stančíková, J., Hlavatá, A., Švec, J., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.10.048 · Cited by 109
mTOR disruption causes intestinal epithelial cell defects and intestinal atrophy postinjury in mice
Sampson, L. L., Davis, A. K., Grogg, M. W., & Zheng, Y. (2015) · The FASEB Journal · doi:10.1096/fj.15-278606 · Cited by 112
Kessler, M., Hoffmann, K., Fritsche, K., Brinkmann, V., Mollenkopf, H., Thieck, O., da Costa, A. R. T., Braicu, E. I., Sehouli, J., Mangler, M., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09144-7 · Cited by 108
Seidlitz, T., Koo, B., & Stange, D. E. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-00662-2 · Cited by 112
Schneeberger, K., Spee, B., Costa, P., Sachs, N., Clevers, H., & Malda, J. (2017) · Biofabrication · doi:10.1088/1758-5090/aa6121 · Cited by 100
Self-citationReynolds, 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
Enteroendocrine and tuft cells support Lgr5 stem cells on Paneth cell depletion
van Es, J. H., Wiebrands, K., López‐Iglesias, C., van de Wetering, M., Zeinstra, L. M., van den Born, M., Korving, J., Sasaki, N., Peters, P. J., van Oudenaarden, A., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801888117 · Cited by 112
Self-citationKim, J., Fei, L., Yin, W.-C., Coquenlorge, S., Rao‐Bhatia, A., Zhang, X., Shi, S. S. W., Lee, J. H., Hahn, N. A., Rizvi, W., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14058-5 · Cited by 111
Essential role of IFN-γ in T cell–associated intestinal inflammation
Eriguchi, Y., Nakamura, K., Yokoi, Y., Sugimoto, R., Takahashi, S., Hashimoto, D., Teshima, T., Ayabe, T., Selsted, M. E., & Ouellette, A. J. (2018) · JCI Insight · doi:10.1172/jci.insight.121886 · Cited by 108
Stem cells and origins of cancer in the upper gastrointestinal tract
Hayakawa, Y., Nakagawa, H., Rustgi, A. K., Que, J., & Wang, T. C. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.05.012 · Cited by 103
Lymphatics and fibroblasts support intestinal stem cells in homeostasis and injury
Goto, N., Goto, S., Imada, S., Hosseini, S., Deshpande, V., & Yilmaz, Ö. H. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.06.013 · Cited by 106
Colonic CD90+ Crypt Fibroblasts Secrete Semaphorins to Support Epithelial Growth
Karpus, O. N., Westendorp, B. F., Vermeulen, J. L. M., Meisner, S., Köster, J., Muncan, V., Wildenberg, M. E., & van den Brink, G. R. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.02.101 · Cited by 95
Wnt Signalling in Gastrointestinal Epithelial Stem Cells
Flanagan, D. J., Austin, C. R., Vincan, E., & Phesse, T. J. (2018) · Genes · doi:10.3390/genes9040178 · Cited by 110
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
Zhang, T., Ding, C., Chen, H., Zhao, J., Chen, Z., Chen, B., Mao, K., Hao, Y., Roulis, M., Xu, H. Y., et al. (2022) · Science Advances · doi:10.1126/sciadv.abl5723 · Cited by 103
Dclk1-expressing tuft cells: critical modulators of the intestinal niche?
Middelhoff, M. A., Westphalen, C. B., Hayakawa, Y., Yan, K. S., Gershon, M. D., Wang, T. C., & Quante, M. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00073.2017 · Cited by 97
Wnt ligands influence tumour initiation by controlling the number of intestinal stem cells
Huels, D. J., Bruens, L., Hodder, M. C., Cammareri, P., Campbell, A. D., Ridgway, R. A., Gay, D. M., Solar-Abboud, M., Faller, W. J., Nixon, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03426-2 · Cited by 103
Gracz, A. D., Fuller, M. K., Wang, F., Li, L., Stelzner, M. G., Dunn, J., Martı́n, M. G., & Magness, S. T. (2013) · Stem Cells · doi:10.1002/stem.1391 · Cited by 101
The cellular niche for intestinal stem cells: a team effort
Zhu, G., Hu, J., & Xi, R. (2021) · Cell Regeneration · doi:10.1186/s13619-020-00061-5 · Cited by 102
Inflation-collapse dynamics drive patterning and morphogenesis in intestinal organoids
Tallapragada, N. P., Cambra, H. M., Wald, T., Jalbert, S. K., Abraham, D. M., Klein, O. D., & Klein, A. M. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.04.002 · Cited by 95
Workshop meeting report Organs-on-Chips: human disease models
van de Stolpe, A., & den Toonder, J. M. J. (2013) · Lab on a Chip · doi:10.1039/c3lc50248a · Cited by 99
Type I Interferons Link Viral Infection to Enhanced Epithelial Turnover and Repair
Sun, L., Miyoshi, H., Origanti, S. S., Nice, T. J., Barger, A. C., Manieri, N. A., Fogel, L. A., French, A. R., Piwnica-Worms, D. R., Piwnica-Worms, H. M., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.11.004 · Cited by 97
Rezza, A., Sennett, R., & Rendl, M. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00012-3 · Cited by 99
Li, B., Lee, C. M., Cadete, M., Zhu, H., Koike, Y., Hock, A., Wu, R., Botts, S. R., Minich, A., Alganabi, M., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1987-1 · Cited by 95
Lin, X., Gaudino, S. J., Jang, K. K., Bahadur, T., Singh, A. A., Banerjee, A., Beaupre, M., Chu, T. H., Wong, H. T., Kim, C.-K., et al. (2022) · Immunity · doi:10.1016/j.immuni.2021.12.016 · Cited by 96
Stem Cells in Repair of Gastrointestinal Epithelia
Andersson-Rolf, A., Zilbauer, M., Koo, B., & Clevers, H. C. (2017) · Physiology · doi:10.1152/physiol.00005.2017 · Cited by 93
Self-citationHallmarks of stemness in mammalian tissues
Beumer, J., & Clevers, H. C. (2024) · Cell stem cell · doi:10.1016/j.stem.2023.12.006 · Cited by 92
Self-citationModeling human development in 3D culture
Ader, M., & Tanaka, E. M. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.06.013 · Cited by 89
Ovary and fimbrial stem cells: biology, niche and cancer origins
Ng, A., & Barker, N. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4056 · Cited by 94
Extrinsic control of Wnt signaling in the intestine
Koch, S. (2017) · Differentiation · doi:10.1016/j.diff.2017.08.003 · Cited by 95
Human colon organoids reveal distinct physiologic and oncogenic Wnt responses
Michels, B. E., Mosa, M. H., Grebbin, B. M., Yepes, D., Darvishi, T., Hausmann, J., Urlaub, H., Zeuzem, S., Kvasnicka, H. M., Oellerich, T., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20180823 · Cited by 92
Self-citationUnraveling intestinal stem cell behavior with models of crypt dynamics
Carulli, A. J., Samuelson, L. C., & Schnell, S. D. (2014) · Integrative Biology · doi:10.1039/c3ib40163d · Cited by 82
Secretory Sorcery: Paneth Cell Control of Intestinal Repair and Homeostasis
Cray, P. L., Sheahan, B. J., & Dekaney, C. M. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.06.006 · Cited by 87
Hypoxic macrophages impair autophagy in epithelial cells through Wnt1: relevance in IBD
Ortiz-Masiá, D., Cosín-Roger, J., Calatayud, S., Hernández, C., Alós, R., Hinojosa, J., Apostolova, N., Álvarez, Á., & Barrachina, M. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.108 · Cited by 78
Dissecting the stem cell niche with organoid models: an engineering-based approach
Murrow, L. M., Weber, R. J., & Gartner, Z. J. (2017) · Development · doi:10.1242/dev.140905 · Cited by 85
Hierarchy and Plasticity in the Intestinal Stem Cell Compartment
Yousefi, M., Li, L., & Lengner, C. J. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.06.006 · Cited by 87
Macrophages as an Emerging Source of Wnt Ligands: Relevance in Mucosal Integrity
Cosín‐Roger, J., Ortiz‐Masiá, D., & Barrachina, M. D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02297 · Cited by 80
Jabaji, Z. B., Sears, C. M., Brinkley, G. J., Lei, N., Joshi, V. S., Wang, J., Lewis, M. S., Stelzner, M. G., Martı́n, M. G., & Dunn, J. (2013) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2012.0710 · Cited by 82
Intestinal epithelium in early life
Frazer, L. C., & Good, M. L. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00579-8 · Cited by 80
The Intestinal Stem Cell Niche: A Central Role for Foxl1-Expressing Subepithelial Telocytes
Kaestner, K. H. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.04.001 · Cited by 83
Establishment of 3D Intestinal Organoid Cultures from Intestinal Stem Cells
Sugimoto, S., & Sato, T. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7021-6_7 · Cited by 79
Holmberg, F., Seidelin, J. B., Yin, X., Mead, B. E., Tong, Z., Li, Y., Karp, J. M., & Nielsen, O. H. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201607260 · Cited by 81
Stem cells in tissues, organoids, and cancers
Wang, X. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03199-x · Cited by 80
Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
Meyer, A. R., Brown, M. E., McGrath, P. S., & Dempsey, P. J. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.12.005 · Cited by 77
Plasticity of Paneth cells and their ability to regulate intestinal stem cells
Mei, X., Gu, M., & Li, M. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01857-7 · Cited by 81
Paneth Cells during Viral Infection and Pathogenesis
Holly, M. K., & Smith, J. G. (2018) · Viruses · doi:10.3390/v10050225 · Cited by 75
Stem Cell Signaling Pathways in the Small Intestine
Takahashi, T., & Shiraishi, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062032 · Cited by 83
Wnt proteins synergize to activate β-catenin signaling
Alok, A., Lei, Z., Jagannathan, N. S., Kaur, S., Harmston, N., Rozen, S., Tucker-Kellogg, L., & Virshup, D. (2017) · Journal of Cell Science · doi:10.1242/jcs.198093 · Cited by 59
Epithelial WNT ligands are essential drivers of intestinal stem cell activation
Zou, W. Y., Blutt, S. E., Zeng, X.-L., Chen, M.-S., Lo, Y.-H., Castillo-Azofeifa, D., Klein, O. D., Shroyer, N. F., Donowitz, M., & Estes, M. K. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.093 · Cited by 73
Lipid-mediated Wnt protein stabilization enables serum-free culture of human organ stem cells
Tüysüz, N., van Bloois, L., van den Brink, S., Begthel, H., Verstegen, M. M. A., Cruz, L. J., Hui, L., van der Laan, L. J. W., de Jonge, J., Vries, R. G. J., et al. (2017) · Nature Communications · doi:10.1038/ncomms14578 · Cited by 74
Self-citationStem cells in homeostasis and cancer of the gut
van der Heijden, M., & Vermeulen, L. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0962-x · Cited by 80
Yun, J., Hansen, S., Morris, O., Madden, D. T., Libeu, C. P., Kumar, A. J., Wehrfritz, C., Nile, A. H., Zhang, Y., Zhou, L., et al. (2023) · Nature Communications · doi:10.1038/s41467-022-35487-9 · Cited by 75
Selenoproteins and oxidative stress-induced inflammatory tumorigenesis in the gut
Barrett, C. W., Short, S. P., & Williams, C. S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2339-2 · Cited by 73
Wnt, RSPO and Hippo Signalling in the Intestine and Intestinal Stem Cells
Kříž, V., & Kořínek, V. (2018) · Genes · doi:10.3390/genes9010020 · Cited by 77
Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine
Ziegler, A. N., Feng, Q., Chidambaram, S., Testai, J. M., Kumari, E., Rothbard, D. E., Constância, M., Sandovici, I., Cominski, T. P., Pang, K. C. H., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.02.011 · Cited by 72
Establishment of Pancreatic Organoids from Normal Tissue and Tumors
Driehuis, E., Gracanin, A., Vries, R. G. J., Clevers, H. C., & Boj, S. F. (2020) · STAR Protocols · doi:10.1016/j.xpro.2020.100192 · Cited by 77
Self-citationXiao, L., Li, X.-X., Chung, H. K., Kalakonda, S., Cai, J., Cao, S., Chen, N., Liu, Y., Rao, J. N., Wang, H., et al. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.05.010 · Cited by 70
Identification, isolation and characterization of human LGR5-positive colon adenoma cells
Dame, M. K., Attili, D., McClintock, S. D., Dedhia, P. H., Ouillette, P. D., Hardt, O., Chin, A. M., Xue, X., Laliberté, J., Katz, E. L., et al. (2018) · Development · doi:10.1242/dev.153049 · Cited by 69
Complexity of the Wnt/β‑catenin pathway: Searching for an activation model
Tortelote, G. G., dos Reis, R. R., Mendes, F. A., & Abreu, J. G. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.08.008 · Cited by 71
Gastrointestinal organoids: How they gut it out
Merker, S. R., Weitz, J., & Stange, D. E. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.08.010 · Cited by 76
Bioengineered Systems and Designer Matrices That Recapitulate the Intestinal Stem Cell Niche
Wang, Y., Kim, R., Hinman, S. S., Zwarycz, B., Magness, S. T., & Allbritton, N. L. (2018) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.01.008 · Cited by 73
Boonekamp, K. E., Dayton, T. L., & Clevers, H. C. (2020) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjaa034 · Cited by 73
Self-citationRees, W. D., Tandun, R., Yau, E., Zachos, N. C., & Steiner, T. S. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.583919 · Cited by 72
Telocytes: An Emerging Component of Stem Cell Niche Microenvironment
Rosa, I., Marini, M., & Manetti, M. (2021) · Journal of Histochemistry & Cytochemistry · doi:10.1369/00221554211025489 · Cited by 70
Crohn's disease-derived monocytes fail to induce Paneth cell defensins
Courth, L. F., Ostaff, M. J., Mailänder‐Sánchez, D., Malek, N. P., Stange, E. F., & Wehkamp, J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510084112 · Cited by 73
Yu, J., & Virshup, D. M. (2014) · Bioscience Reports · doi:10.1042/bsr20140119 · Cited by 72
Kandasamy, J., Huda, S. A., Ambalavanan, N., & Jilling, T. (2014) · Pathophysiology · doi:10.1016/j.pathophys.2014.01.001 · Cited by 70
Anti-LRP5/6 VHHs promote differentiation of Wnt-hypersensitive intestinal stem cells
Fenderico, N., van Scherpenzeel, R. C., Goldflam, M., Proverbio, D., Jordens, I., Kralj, T., Stryeck, S., Bass, T. Z., Hermans, G., Ullman, C. G., et al. (2019) · Nature Communications · doi:10.1038/s41467-018-08172-z · Cited by 64
Reactive Oxygen Species in intestinal stem cell metabolism, fate and function
Morris, O., & Jasper, H. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.02.015 · Cited by 70
Aging of intestinal stem cells
Nalapareddy, K., Zheng, Y., & Geiger, H. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.02.003 · Cited by 70
The ErbB4 Ligand Neuregulin-4 Protects against Experimental Necrotizing Enterocolitis
McElroy, S. J., Castle, S. L., Bernard, J. K., Almohazey, D., Hunter, C. J., Bell, B. A., Alam, D. A., Wang, L. W., Ford, H. R., & Frey, M. R. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.06.015 · Cited by 68
Epithelial stem cells and intestinal cancer
Tan, S., & Barker, N. (2014) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2014.02.005 · Cited by 66
Hallmarks of intestinal stem cells
Baulies, A., Angelis, N., & Li, V. S. W. (2020) · Development · doi:10.1242/dev.182675 · Cited by 71
Fatehullah, A., Appleton, P. L., & Näthke, I. S. (2013) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0014 · Cited by 65
Source and Impact of the EGF Family of Ligands on Intestinal Stem Cells
Abud, H. E., Chan, W. H., & Jardé, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.685665 · Cited by 71
Jang, B. G., Lee, B. L., & Kim, W. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082390 · Cited by 64
Intestinal commensal microbiota and cytokines regulate Fut2 + Paneth cells for gut defense
Kamioka, M., Goto, Y., Nakamura, K., Yokoi, Y., Sugimoto, R., Ohira, S., Kurashima, Y., Umemoto, S., Sato, S., Kunisawa, J., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2115230119 · Cited by 62
Abo, H., Chassaing, B., Harusato, A., Quirós, M., Brazil, J. C., Ngo, V. L., Viennois, É., Merlin, D., Gewirtz, A. T., Nusrat, A., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14258-z · Cited by 63
Mammalian Intestinal Development and Differentiation—The State of the Art
Kolev, H. M., & Kaestner, K. H. (2023) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2023.07.011 · Cited by 63
Snai1 regulates cell lineage allocation and stem cell maintenance in the mouse intestinal epithelium
Horvay, K., Jardé, T., Casagranda, F., Perreau, V. M., Haigh, K., Nefzger, C. M., Akhtar, R., Gridley, T., Berx, G., Haigh, J. J., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201490881 · Cited by 60
Wnt Signaling in Stem Cells and Cancer Stem Cells: A Tale of Two Coactivators
Kahn, M. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.11.007 · Cited by 62
CCN1 interacts with integrins to regulate intestinal stem cell proliferation and differentiation
Won, J. H., Choi, J. S., & Jun, J.-I. (2022) · Nature Communications · doi:10.1038/s41467-022-30851-1 · Cited by 62
Tissue Engineering the Small Intestine
Spurrier, R. G., & Grikscheit, T. C. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.01.028 · Cited by 59
CDC42 Inhibition Suppresses Progression of Incipient Intestinal Tumors
Sakamori, R., Yu, S., Zhang, X., Hoffman, A., Sun, J., Das, S., Vedula, P., Li, G., Fu, J., Walker, F., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-14-0267 · Cited by 58
Wnt Signaling Mediates the Aging-Induced Differentiation Impairment of Intestinal Stem Cells
Cui, H., Tang, D., Garside, G. B., Zeng, T., Wang, Y., Tao, Z., Zhang, L., & Tao, S. (2019) · Stem Cell Reviews and Reports · doi:10.1007/s12015-019-09880-9 · Cited by 57
The role of the Wnt signaling pathway in cancer stem cells: prospects for drug development
Kahn, M., & Kim, Y. (2014) · Research and Reports in Biochemistry · doi:10.2147/rrbc.s53823 · Cited by 59
Quiescence Exit of Tert+ Stem Cells by Wnt/β-Catenin Is Indispensable for Intestinal Regeneration
Suh, H. N., Kim, M. J., Jung, Y., Lien, E. M., Jun, S., & Park, J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.118 · Cited by 57
Wu, A., Yu, B., Zhang, K., Xu, Z., Wu, D., He, J., Luo, J., Luo, Y., Yu, J., Zheng, P., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2233-6 · Cited by 57
Das, S., Yu, S., Sakamori, R., Vedula, P., Feng, Q., Flores, J., Hoffman, A., Fu, J., Stypulkowski, E., Rodriguez, A., et al. (2015) · Development · doi:10.1242/dev.121046 · Cited by 54
Id2 controls specification of Lgr5+ intestinal stem cell progenitors during gut development
Nigmatullina, L., Norkin, M. N., Dzama, M. M., Messner, B., Sayols, S., & Soshnikova, N. V. (2017) · The EMBO Journal · doi:10.15252/embj.201694959 · Cited by 55
Smooth muscle contributes to the development and function of a layered intestinal stem cell niche
McCarthy, N., Tie, G., Madha, S., He, R., Kraiczy, J., Maglieri, A., & Shivdasani, R. A. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.02.012 · Cited by 55
Wnt Signalling in Intestinal Stem Cells: Lessons from Mice and Flies
Perochon, J., Carroll, L. R., & Cordero, J. B. (2018) · Genes · doi:10.3390/genes9030138 · Cited by 55
Liang, S., Li, X., & Wang, X. (2019) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x14666190429143734 · Cited by 54
Metadata
- Authors
- Farin, H. F., Van Es, J. H., & Clevers, H.
- Affiliations
- University Medical Center Utrecht (NL)
- Corresponding author
- Clevers, Hans
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2012-12
- Volume
- 143
- Issue
- 6
- Pages
- 1518-1529.e7
- ISSN
- 0016-5085 (ISSN-L)
- OpenAlex
- W2038714514
- Cited by
- 655
- References
- 55
- Citations by year
- 2026: 25 · 2025: 38 · 2024: 39 · 2023: 54 · 2022: 48 · 2021: 68 · 2020: 56 · 2019: 55 · 2018: 57 · 2017: 57 · 2016: 34 · 2015: 41 · 2014: 37 · 2013: 41 · 2012: 4
- FWCI
- 15.80
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (submittedVersion)
- Funders
- European Molecular Biology Organization
- Top Institute Pharma
- Topics
- 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
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Keywords
- Wnt signaling, Wnt3, intestinal stem cells, Paneth cells, R-spondin, Atoh1, mesenchymal cells, intestinal homeostasis
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Epithelial Cells, Homeostasis, Intestine, Small, Mice, Transgenic, Stem Cells, Signal Transduction, Paneth Cells, Models, Animal, Mice, Wnt3 Protein, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review