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Wnt/β-Catenin Signaling Controls Spatio-Temporal Elasticity Patterns in Extracellular Matrix during Hydra Morphogenesis

https://doi.org/10.1101/214718
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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/bies.1101openalex-snapshot
Hydra and Niccolo Paganini (1782–1840)—two peas in a pod? The molecular basis of extracellular matrix structure in the invertebrate, Hydra
inferredcites →https://doi.org/10.1002/bies.200800183openalex-snapshot
Hydra and the evolution of stem cells
inferredcites →https://doi.org/10.1002/jez.1402000311openalex-snapshot
Budding inHydra attenuata:Bud stages and fate map
inferredcites →https://doi.org/10.1007/bf00335643openalex-snapshot
An ultrastructural examination of the mesoglea of Hydra
inferredcites →https://doi.org/10.1007/s00427-005-0038-3openalex-snapshot
Gastrulation in the sea anemone Nematostella vectensis occurs by invagination and immigration: an ultrastructural study
inferredcites →https://doi.org/10.1007/s12551-019-00528-zopenalex-snapshot
Frustrated differentiation of mesenchymal stem cells
inferredcites →https://doi.org/10.1016/0012-1606(67)90039-5openalex-snapshot
Tissue dynamics of steady state growth in Hydra littoralis
inferredcites →https://doi.org/10.1016/0012-1606(91)90277-aopenalex-snapshot
Pattern of epithelial cell cycling in hydra
inferredcites →https://doi.org/10.1016/bs.ctdb.2018.03.006openalex-snapshot
Extracellular Matrix (ECM) and the Sculpting of Embryonic Tissues
inferredcites →https://doi.org/10.1016/j.cell.2014.09.038openalex-snapshot
Genome-wide RNA Tomography in the Zebrafish Embryo
inferredcites →https://doi.org/10.1016/j.cub.2020.02.027openalex-snapshot
Cellular Heterogeneity in Pressure and Growth Emerges from Tissue Topology and Geometry
inferredcites →https://doi.org/10.1016/j.ejcb.2006.05.007openalex-snapshot
Genetic screen for signal peptides in Hydra reveals novel secreted proteins and evidence for non-classical protein secretion
inferredcites →https://doi.org/10.1016/j.immuni.2006.12.007openalex-snapshot
Wnt Signaling Induces Matrix Metalloproteinase Expression and Regulates T Cell Transmigration
inferredcites →https://doi.org/10.1016/j.semcdb.2009.09.008openalex-snapshot
Immortality and the base of multicellular life: Lessons from cnidarian stem cells
inferredcites →https://doi.org/10.1016/j.stem.2013.06.005openalex-snapshot
A Role for Matrix Metalloproteinases in Regulating Mammary Stem Cell Function via the Wnt Signaling Pathway
inferredcites →https://doi.org/10.1016/j.ydbio.2006.04.003openalex-snapshot
Dickkopf related genes are components of the positional value gradient in Hydra
inferredcites →https://doi.org/10.1016/j.ydbio.2017.09.005openalex-snapshot
β-Catenin acts in a position-independent regeneration response in the simple eumetazoan Hydra
inferredcites →https://doi.org/10.1016/j.zool.2007.11.004openalex-snapshot
The extracellular matrix of hydra is a porous sheet and contains type IV collagen
inferredcites →https://doi.org/10.1016/s0006-3495(02)75620-8openalex-snapshot
Determination of Elastic Moduli of Thin Layers of Soft Material Using the Atomic Force Microscope
inferredcites →https://doi.org/10.1016/s0006-3495(04)74375-1openalex-snapshot
Dynamic Elastic Modulus of Porcine Articular Cartilage Determined at Two Different Levels of Tissue Organization by Indentation-Type Atomic Force Microscopy
inferredcites →https://doi.org/10.1016/s0022-2836(95)80065-4openalex-snapshot
Type I collagen packing, conformation of the triclinic unit cell
inferredcites →https://doi.org/10.1016/s1534-5807(02)00197-1openalex-snapshot
Convergent Extension
inferredcites →https://doi.org/10.1021/la9037414openalex-snapshot
Spatially Resolved Investigation of Solution Cast Nanoparticle Films by X-ray Scattering and Multidimensional Data Set Classification
inferredcites →https://doi.org/10.1038/282878a0openalex-snapshot
Quasi-hexagonal molecular packing in collagen fibrils
inferredcites →https://doi.org/10.1038/nature25742openalex-snapshot
Tissue stiffening coordinates morphogenesis by triggering collective cell migration in vivo
inferredcites →https://doi.org/10.1038/nmeth.2089openalex-snapshot
NIH Image to ImageJ: 25 years of image analysis
inferredcites →https://doi.org/10.1038/nn.4394openalex-snapshot
Mechanosensing is critical for axon growth in the developing brain
inferredcites →https://doi.org/10.1038/nrm3904openalex-snapshot
Remodelling the extracellular matrix in development and disease
inferredcites →https://doi.org/10.1038/nrneph.2015.88openalex-snapshot
Wnt/β-catenin signalling and podocyte dysfunction in proteinuric kidney disease
inferredcites →https://doi.org/10.1038/sj.leu.2405030openalex-snapshot
Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes
inferredcites →https://doi.org/10.1038/srep24264openalex-snapshot
Frequent mechanical stress suppresses proliferation of mesenchymal stem cells from human bone marrow without loss of multipotency
inferredcites →https://doi.org/10.1039/c9sm01893jopenalex-snapshot
A subtle relationship between substrate stiffness and collective migration of cell clusters
inferredcites →https://doi.org/10.1042/ebc20190021openalex-snapshot
Extracellular matrix and morphogenesis in cnidarians: a tightly knit relationship
inferredcites →https://doi.org/10.1063/1.2776850openalex-snapshot
In situ observation of nanoparticle ordering at the air-water-substrate boundary in colloidal solutions using x-ray nanobeams
inferredcites →https://doi.org/10.1073/pnas.0502718103openalex-snapshot
Microfibrillar structure of type I collagen in situ
inferredcites →https://doi.org/10.1073/pnas.0812847106openalex-snapshot
Wnt/β-Catenin and noncanonical Wnt signaling interact in tissue evagination in the simple eumetazoan Hydra
inferredcites →https://doi.org/10.1073/pnas.1018109108openalex-snapshot
Autoregulatory and repressive inputs localize Hydra Wnt3 to the head organizer
inferredcites →https://doi.org/10.1073/pnas.1115083109openalex-snapshot
Tissue inhibitor of metalloproteinase-1 (TIMP-1) regulates mesenchymal stem cells through let-7f microRNA and Wnt/β-catenin signaling
inferredcites →https://doi.org/10.1074/jbc.m111.229427openalex-snapshot
Matrix Metalloproteinase (MMP)-9 Induced by Wnt Signaling Increases the Proliferation and Migration of Embryonic Neural Stem Cells at Low O2 Levels
inferredcites →https://doi.org/10.1074/jbc.m401460200openalex-snapshot
Unique Catabolic Pathway of Glycosphingolipids in a Hydrozoan, Hydra magnipapillata, Involving Endoglycoceramidase
inferredcites →https://doi.org/10.1074/jbc.m500374200openalex-snapshot
Wnt-7a Up-regulates Matrix Metalloproteinase-12 Expression and Promotes Cell Proliferation in Corneal Epithelial Cells during Wound Healing
inferredcites →https://doi.org/10.1083/jcb.201207148openalex-snapshot
Substrate stiffness regulates cadherin-dependent collective migration through myosin-II contractility
inferredcites →https://doi.org/10.1088/1748-0221/6/01/c01069openalex-snapshot
MAXIPIX, a fast readout photon-counting X-ray area detector for synchrotron applications
inferredcites →https://doi.org/10.1093/molbev/msv079openalex-snapshot
A Comprehensive Transcriptomic and Proteomic Analysis of Hydra Head Regeneration
inferredcites →https://doi.org/10.1115/1.2893754openalex-snapshot
Regular Pyramid Punch Problem
inferredcites →https://doi.org/10.1164/rccm.201204-0754ocopenalex-snapshot
Acellular Normal and Fibrotic Human Lung Matrices as a Culture System for In Vitro Investigation
inferredcites →https://doi.org/10.1242/dev.01848openalex-snapshot
Formation of the head organizer in hydra involves the canonical Wnt pathway
inferredcites →https://doi.org/10.1242/dev.02265openalex-snapshot
An ancient Wnt-Dickkopf antagonism inHydra
inferredcites →https://doi.org/10.1242/dev.127.21.4669openalex-snapshot
Molecular, biochemical and functional analysis of a novel and developmentally important fibrillar collagen (Hcol-I) in hydra
inferredcites →https://doi.org/10.1242/dev.127.4.907openalex-snapshot
A novel hydra matrix metalloproteinase (HMMP) functions in extracellular matrix degradation, morphogenesis and the maintenance of differentiated cells in the foot process
inferredcites →https://doi.org/10.1242/dev.129.6.1521openalex-snapshot
Epithelial morphogenesis in hydra requires de novo expression of extracellular matrix components and matrix metalloproteinases
inferredcites →https://doi.org/10.1242/jcs.087239openalex-snapshot
In vivo imaging of basement membrane movement: ECM patterning shapesHydrapolyps
inferredcites →https://doi.org/10.1258/002367770781036463openalex-snapshot
Mass culture of hydra: an improved method and its application to other aquatic invertebrates
inferredcites →https://doi.org/10.1387/ijdb.113445msopenalex-snapshot
Components, structure, biogenesis and function of the Hydra extracellular matrix in regeneration, pattern formation and cell differentiation
inferredcites →https://doi.org/10.3791/2911openalex-snapshot
Micro-Mechanical Characterization of Lung Tissue Using Atomic Force Microscopy

What points at this work

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

inferred← citeshttps://doi.org/10.1101/2021.02.05.429954openalex-snapshot
Two interconnected patterning loops are required for body axis and head organizer formation in Hydra
inferred← citeshttps://doi.org/10.1101/2021.09.13.460125openalex-snapshot
Mutual Inhibition Model of pattern formation: The role of Wnt-Dickkopf interactions in driving Hydra body axis formation
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