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A Dynamic WNT/β-CATENIN Signaling Environment Leads to WNT-Independent and WNT-Dependent Proliferation of Embryonic Intestinal Progenitor Cells

https://doi.org/10.1016/j.stemcr.2016.09.004

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvg.20596openalex-snapshot

Generation of mice with a conditional null allele for Tbx2

inferredcites →https://doi.org/10.1002/dvg.20651openalex-snapshot

Generation of mice with a conditional null allele for Wntless

inferredcites →https://doi.org/10.1002/gene.20042openalex-snapshot

Tissue‐specific and inducible Cre‐mediated recombination in the gut epithelium

inferredcites →https://doi.org/10.1002/j.1460-2075.1988.tb03249.xopenalex-snapshot

Cell binding function of E‐cadherin is regulated by the cytoplasmic domain.

inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb03563.xopenalex-snapshot

The cytoplasmic domain of the cell adhesion molecule uvomorulin associates with three independent proteins structurally related in different species.

inferredcites →https://doi.org/10.1002/jcb.23324openalex-snapshot

Lrp5 and Lrp6 play compensatory roles in mouse intestinal development

inferredcites →https://doi.org/10.1006/dbio.1999.9601openalex-snapshot

Anterior Endoderm Is Sufficient to Rescue Foregut Apoptosis and Heart Tube Morphogenesis in an Embryo Lacking Retinoic Acid

inferredcites →https://doi.org/10.1016/0092-8674(92)90404-zopenalex-snapshot

Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain

inferredcites →https://doi.org/10.1016/j.bbaexp.2003.10.009openalex-snapshot

R-spondin, a novel gene with thrombospondin type 1 domain, was expressed in the dorsal neural tube and affected in Wnts mutants

inferredcites →https://doi.org/10.1016/j.cell.2004.07.024openalex-snapshot

Evidence for an Expansion-Based Temporal Shh Gradient in Specifying Vertebrate Digit Identities

inferredcites →https://doi.org/10.1016/j.cell.2015.03.041openalex-snapshot

Bending Gradients: How the Intestinal Stem Cell Gets Its Home

inferredcites →https://doi.org/10.1016/j.celrep.2016.03.088openalex-snapshot

Wnt Ligands Secreted by Subepithelial Mesenchymal Cells Are Essential for the Survival of Intestinal Stem Cells and Gut Homeostasis

inferredcites →https://doi.org/10.1016/j.cub.2012.08.002openalex-snapshot

Cancer Biology: A New RING to Wnt Signaling

inferredcites →https://doi.org/10.1016/j.devcel.2007.12.003openalex-snapshot

The Retromer Complex Influences Wnt Secretion by Recycling Wntless from Endosomes to the Trans-Golgi Network

inferredcites →https://doi.org/10.1016/j.devcel.2009.05.012openalex-snapshot

Sox17 Regulates Organ Lineage Segregation of Ventral Foregut Progenitor Cells

inferredcites →https://doi.org/10.1016/j.devcel.2009.06.016openalex-snapshot

Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases

inferredcites →https://doi.org/10.1016/j.jcmgh.2015.11.010openalex-snapshot

GATA4 Regulates Epithelial Cell Proliferation to Control Intestinal Growth and Development in Mice

inferredcites →https://doi.org/10.1016/j.stem.2015.09.019openalex-snapshot

Polycomb Complex PRC1 Preserves Intestinal Stem Cell Identity by Sustaining Wnt/β-Catenin Transcriptional Activity

inferredcites →https://doi.org/10.1016/j.stemcr.2013.12.012openalex-snapshot

Wnt Secretion from Epithelial Cells and Subepithelial Myofibroblasts Is Not Required in the Mouse Intestinal Stem Cell Niche In Vivo

inferredcites →https://doi.org/10.1016/j.ydbio.2010.09.010openalex-snapshot

Fibroblast growth factor 10 represses premature cell differentiation during establishment of the intestinal progenitor niche

inferredcites →https://doi.org/10.1016/j.ydbio.2012.06.005openalex-snapshot

E-cadherin is required for intestinal morphogenesis in the mouse

inferredcites →https://doi.org/10.1016/j.ydbio.2013.03.010openalex-snapshot

Wntless is required for peripheral lung differentiation and pulmonary vascular development

inferredcites →https://doi.org/10.1016/j.ydbio.2013.11.018openalex-snapshot

Sox17 is required for normal pulmonary vascular morphogenesis

inferredcites →https://doi.org/10.1016/j.ydbio.2014.05.017openalex-snapshot

GATA4 and GATA6 regulate intestinal epithelial cytodifferentiation during development

inferredcites →https://doi.org/10.1016/s0092-8674(03)00002-3openalex-snapshot

Twist Regulates Cytokine Gene Expression through a Negative Feedback Loop that Represses NF-κB Activity

inferredcites →https://doi.org/10.1016/s0925-4773(02)00090-4openalex-snapshot

E-cadherin is a survival factor for the lactating mouse mammary gland

inferredcites →https://doi.org/10.1038/1270openalex-snapshot

Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4

inferredcites →https://doi.org/10.1038/35035117openalex-snapshot

LDL-receptor-related proteins in Wnt signal transduction

inferredcites →https://doi.org/10.1038/35077108openalex-snapshot

LDL-receptor-related protein 6 is a receptor for Dickkopf proteins

inferredcites →https://doi.org/10.1038/35083081openalex-snapshot

Novel mechanism of Wnt signalling inhibition mediated by Dickkopf-1 interaction with LRP6/Arrow

inferredcites →https://doi.org/10.1038/nature07602openalex-snapshot

Crypt stem cells as the cells-of-origin of intestinal cancer

inferredcites →https://doi.org/10.1038/ncb1678openalex-snapshot

Wingless secretion requires endosome-to-Golgi retrieval of Wntless/Evi/Sprinter by the retromer complex

inferredcites →https://doi.org/10.1038/sj.onc.1210057openalex-snapshot

Transgenic Wnt/TCF pathway reporters: all you need is Lef?

inferredcites →https://doi.org/10.1053/j.gastro.2007.04.072openalex-snapshot

Phases of Canonical Wnt Signaling During the Development of Mouse Intestinal Epithelium

inferredcites →https://doi.org/10.1053/j.gastro.2012.08.031openalex-snapshot

Redundant Sources of Wnt Regulate Intestinal Stem Cells and Promote Formation of Paneth Cells

inferredcites →https://doi.org/10.1073/pnas.1205669109openalex-snapshot

Hedgehog-responsive mesenchymal clusters direct patterning and emergence of intestinal villi

inferredcites →https://doi.org/10.1073/pnas.1311760110openalex-snapshot

Lung epithelial branching program antagonizes alveolar differentiation

inferredcites →https://doi.org/10.1073/pnas.1311847110openalex-snapshot

Sox9 plays multiple roles in the lung epithelium during branching morphogenesis

inferredcites →https://doi.org/10.1073/pnas.87.11.4246openalex-snapshot

Uvomorulin-catenin complex formation is regulated by a specific domain in the cytoplasmic region of the cell adhesion molecule.

inferredcites →https://doi.org/10.1074/jbc.m204935200openalex-snapshot

cis Elements of the Villin Gene Control Expression in Restricted Domains of the Vertical (Crypt) and Horizontal (Duodenum, Cecum) Axes of the Intestine

inferredcites →https://doi.org/10.1083/jcb.200311021openalex-snapshot

SOX9 is an intestine crypt transcription factor, is regulated by the Wnt pathway, and represses the CDX2 and MUC2 genes

inferredcites →https://doi.org/10.1083/jcb.200704152openalex-snapshot

Sox9 regulates cell proliferation and is required for Paneth cell differentiation in the intestinal epithelium

inferredcites →https://doi.org/10.1091/mbc.e08-02-0187openalex-snapshot

R-Spondin Family Members Regulate the Wnt Pathway by a Common Mechanism

inferredcites →https://doi.org/10.1093/jnci/djt444openalex-snapshot

KRAS and Cancer Stem Cells in APC-Mutant Colorectal Cancer

inferredcites →https://doi.org/10.1101/gad.267103openalex-snapshot

Canonical Wnt signals are essential for homeostasis of the intestinal epithelium

inferredcites →https://doi.org/10.1126/science.1238842openalex-snapshot

Villification: How the Gut Gets Its Villi

inferredcites →https://doi.org/10.1126/science.275.5307.1784openalex-snapshot

Constitutive Transcriptional Activation by a β-Catenin-Tcf Complex in APC −/− Colon Carcinoma

inferredcites →https://doi.org/10.1126/science.275.5307.1787openalex-snapshot

Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC

inferredcites →https://doi.org/10.1128/mcb.13.4.2235openalex-snapshot

Mouse GATA-4: a Retinoic Acid-Inducible GATA-Binding Transcription Factor Expressed in Endodermally Derived Tissues and Heart

inferredcites →https://doi.org/10.1128/mcb.22.4.1184-1193.2002openalex-snapshot

Negative Feedback Loop of Wnt Signaling through Upregulation of Conductin/Axin2 in Colorectal and Liver Tumors

inferredcites →https://doi.org/10.1186/1471-230x-8-57openalex-snapshot

Wnt-reporter expression pattern in the mouse intestine during homeostasis

inferredcites →https://doi.org/10.1242/dev.065789openalex-snapshot

Cell dynamics in fetal intestinal epithelium: implications for intestinal growth and morphogenesis

inferredcites →https://doi.org/10.1242/dev.121046openalex-snapshot

Rab8a vesicles regulate Wnt ligand delivery and Paneth cell maturation at the intestinal stem cell niche

inferredcites →https://doi.org/10.1242/dev.127.16.3457openalex-snapshot

Abnormal gastrointestinal development in PDGF-A and PDGFR-α deficient mice implicates a novel mesenchymal structure with putative instructive properties in villus morphogenesis

inferredcites →https://doi.org/10.1242/dev.128.8.1253openalex-snapshot

Inactivation of the β-catenin gene by Wnt1-Cre -mediated deletion results in dramatic brain malformation and failure of craniofacial development

inferredcites →https://doi.org/10.1242/dev.130112openalex-snapshot

Villification in the mouse: Bmp signals control intestinal villus patterning

inferredcites →https://doi.org/10.1242/jcs.015958openalex-snapshot

In vivo role of lipid adducts on Wingless

inferredcites →https://doi.org/10.1242/jcs.107.12.3569openalex-snapshot

Regulation of cell number in the mammalian gastrointestinal tract: the importance of apoptosis

inferredcites →https://doi.org/10.1371/journal.pone.0023139openalex-snapshot

Contrasting Expression of Canonical Wnt Signaling Reporters TOPGAL, BATGAL and Axin2LacZ during Murine Lung Development and Repair

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4661071openalex-extracted

Dual States of Bmi1-Expressing Intestinal Stem Cells Drive Epithelial Development

inferred← citeshttps://doi.org/10.1002/wdev.317openalex-snapshot

Blueprint for an intestinal villus: Species‐specific assembly required

inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11178-xopenalex-snapshot

LRPs in Bone Homeostasis and Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00007-4openalex-snapshot

WNT Signaling in the Intestine: Development, Homeostasis, Disease

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.12.001openalex-snapshot

Signals and forces shaping organogenesis of the small intestine

inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102116openalex-snapshot

Stand by me: Fibroblasts regulation of the intestinal epithelium during development and homeostasis

inferred← citeshttps://doi.org/10.1016/j.chphi.2026.101128openalex-snapshot

Benzoylated α-mangostin derivatives targeting the allosteric pocket of β-Catenin: An integrated pharmacophore modeling and molecular simulation study

inferred← citeshttps://doi.org/10.1016/j.devcel.2018.06.011openalex-snapshot

Radial WNT5A-Guided Post-mitotic Filopodial Pathfinding Is Critical for Midgut Tube Elongation

inferred← citeshttps://doi.org/10.1016/j.devcel.2020.11.010openalex-snapshot

Single-Cell Sequencing of Developing Human Gut Reveals Transcriptional Links to Childhood Crohn’s Disease

inferred← citeshttps://doi.org/10.1016/j.devcel.2025.03.014openalex-snapshot

Dual states of murine Bmi1-expressing intestinal stem cells drive epithelial development utilizing non-canonical Wnt signaling

inferred← citeshttps://doi.org/10.1016/j.diff.2019.01.001openalex-snapshot

Stromal control of intestinal development and the stem cell niche

inferred← citeshttps://doi.org/10.1016/j.jphs.2018.07.012openalex-snapshot

Butyrate suppresses abnormal proliferation in colonic epithelial cells under diabetic state by targeting HMGB1

inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.01.011openalex-snapshot

Morphogenesis and maturation of the embryonic and postnatal intestine

inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.01.004openalex-snapshot

Regulation and functions of cell division in the intestinal tissue

inferred← citeshttps://doi.org/10.1016/j.stemcr.2017.11.012openalex-snapshot

In Vitro Induction and In Vivo Engraftment of Lung Bud Tip Progenitor Cells Derived from Human Pluripotent Stem Cells

inferred← citeshttps://doi.org/10.1016/j.tcb.2020.11.010openalex-snapshot

Mesenchymal Niches for Digestive Organ Development, Homeostasis, and Disease

inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.08.009openalex-snapshot

Proliferation in the developing intestine is regulated by the endosomal protein Endotubin

inferred← citeshttps://doi.org/10.1038/s41418-020-00665-zopenalex-snapshot

Organoid-based modeling of intestinal development, regeneration, and repair

inferred← citeshttps://doi.org/10.1038/s41467-022-28369-7openalex-snapshot

Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling

inferred← citeshttps://doi.org/10.1038/s41467-023-36228-2openalex-snapshot

Epigenetic control of cellular crosstalk defines gastrointestinal organ fate and function

inferred← citeshttps://doi.org/10.1038/s42003-022-03079-4openalex-snapshot

Ret kinase-mediated mechanical induction of colon stem cells by tumor growth pressure stimulates cancer progression in vivo

inferred← citeshttps://doi.org/10.1101/2022.09.30.509798openalex-snapshot

Dual states of Bmi1-expressing intestinal stem cells drive epithelial development and tissue regeneration

inferred← citeshttps://doi.org/10.1186/s12915-023-01667-2openalex-snapshot

A stromal lineage maintains crypt structure and villus homeostasis in the intestinal stem cell niche

inferred← citeshttps://doi.org/10.1186/s41232-024-00355-0openalex-snapshot

Regulation of intestinal epithelial homeostasis by mesenchymal cells

inferred← citeshttps://doi.org/10.1242/dev.182675openalex-snapshot

Hallmarks of intestinal stem cells

inferred← citeshttps://doi.org/10.1242/dev.200693openalex-snapshot

Stable iPSC-derived NKX2-1+ lung bud tip progenitor organoids give rise to airway and alveolar cell types

inferred← citeshttps://doi.org/10.12717/dr.2019.23.4.305openalex-snapshot

Epithelial-Mesenchymal Interactions for the Development of Intestinal Villi

inferred← citeshttps://doi.org/10.15252/embj.201694959openalex-snapshot

Id2 controls specification of Lgr5+ intestinal stem cell progenitors during gut development

inferred← citeshttps://doi.org/10.3390/biomedicines12030668openalex-snapshot

Subepithelial Stromal Cells: Their Roles and Interactions with Intestinal Epithelial Cells during Gut Mucosal Homeostasis and Regeneration

inferred← citeshttps://doi.org/10.3390/cancers11081162openalex-snapshot

A Role for the WNT Co-Receptor LRP6 in Pathogenesis and Therapy of Epithelial Cancers

inferred← citeshttps://doi.org/10.5306/wjco.v13.i3.168openalex-snapshot

Intestinal Wnt in the transition from physiology to oncology

inferred← citeshttps://doi.org/10.6084/m9.figshare.23908727openalex-snapshot

Additional file 1 of A stromal lineage maintains crypt structure and villus homeostasis in the intestinal stem cell niche

inferred← citeshttps://doi.org/10.6084/m9.figshare.23908730openalex-snapshot

Additional file 2 of A stromal lineage maintains crypt structure and villus homeostasis in the intestinal stem cell niche

inferred← citeshttps://doi.org/10.70675/298c6b66z88a6z4a34z9437zf6ee84c0f295openalex-snapshot

Cell mechanics contribution to crypt-villus axis development and maintenance

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