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Collagen fibrillogenesis in situ: Fibril segments undergo post‐depositional modifications resulting in linear and lateral growth during matrix development

https://doi.org/10.1002/aja.1002020303
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Outgoing claims: the papers this work cites, builds on, or argues with.

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A study of the growth of normal and iodinated collagen fibrils in vitro using electron microscope autoradiography
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The regulation of size and form in the assembly of collagen fibrils in vivo
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A series of normal stages in the development of the chick embryo
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Growth and development of collagen fibrils in connective tissue
inferredcites →https://doi.org/10.1007/978-1-4615-3770-0_2openalex-snapshot
Collagen
inferredcites →https://doi.org/10.1007/978-1-4615-3770-0_8openalex-snapshot
Matrix Assembly
inferredcites →https://doi.org/10.1016/0003-9861(92)90562-bopenalex-snapshot
cDNA clone to chick corneal chondroitin/dermatan sulfate proteoglycan reveals identity to decorin
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Complete nucleotide sequence of the messenger RNA coding for chicken muscle glyceraldehyde-3-phosphate dehydrogenase
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Collagen fibril assembly by corneal fibroblasts in three-dimensional collagen gel cultures: Small-diameter heterotypic fibrils are deposited in the absence of keratan sulfate proteoglycan
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Multistep assembly of type I collagen fibrils
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Collagen fibril morphology in developing chick metatarsal tendoms: 1. X-ray diffraction studies
inferredcites →https://doi.org/10.1016/0141-8130(82)90082-4openalex-snapshot
Collagen fibril morphology in developing chick metatarsal tendon: 2. Electron microscope studies
inferredcites →https://doi.org/10.1016/0141-8130(85)90034-0openalex-snapshot
Morphological characterization of tendon development during chick embryogenesis: measurement of birefringence retardation
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Structural and mechanical assessment of developing chick tendon
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Site-directed mutagenesis by overlap extension using the polymerase chain reaction
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Collagen fibril assembly and deposition in the developing dermis: Segmental deposition in extracellular compartments
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Fundamentals of Interstitial Collagen Self-Assembly
inferredcites →https://doi.org/10.1016/b978-0-12-775170-2.50009-3openalex-snapshot
Collagen Fibril Assembly, Deposition, and Organization into Tissue-Specific Matrices
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The Extracellular Matrix in Development
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Axial mass distributions of collagen fibrils grown in vitro: Results for the end regions of early fibrils
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Type V collagen and Bowman's membrane. Quantitation of mRNA in corneal epithelium and stroma.
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Assembly of collagen fibrils de novo by cleavage of the type I pC-collagen with procollagen C-proteinase. Assay of critical concentration demonstrates that collagen self-assembly is a classical example of an entropy-driven process.
inferredcites →https://doi.org/10.1016/s0022-2836(05)80015-4openalex-snapshot
Native collagen fibrils from echinoderms are molecularly bipolar
inferredcites →https://doi.org/10.1016/s0022-2836(05)80016-6openalex-snapshot
Vertebrate (chick) collagen fibrils formed in Vivo can exhibit a reversal in molecular polarity
inferredcites →https://doi.org/10.1016/s0889-1605(86)80023-4openalex-snapshot
Topographies of extracytoplasmic compartments in developing chick tendon fibroblasts
inferredcites →https://doi.org/10.1042/bj1950229openalex-snapshot
Absence of the iron-containing superoxide dismutase in mitochondria from mustard (Brassica campestris)
inferredcites →https://doi.org/10.1042/bj2180229openalex-snapshot
The periphery of the developing collagen fibril. Quantitative relationships with dermatan sulphate and other surface-associated species
inferredcites →https://doi.org/10.1042/bj2680339openalex-snapshot
Collagen fibrils in vitro grow from pointed tips in the C- to N-terminal direction
inferredcites →https://doi.org/10.1073/pnas.81.10.3014openalex-snapshot
Synthesis and characterization of cDNA encoding a cartilage-specific short collagen.
inferredcites →https://doi.org/10.1073/pnas.86.12.4549openalex-snapshot
Collagen fibrillogenesis in situ: fibril segments are intermediates in matrix assembly.
inferredcites →https://doi.org/10.1073/pnas.87.7.2725openalex-snapshot
Analysis of cytokine mRNA and DNA: detection and quantitation by competitive polymerase chain reaction.
inferredcites →https://doi.org/10.1073/pnas.89.20.9855openalex-snapshot
Growing tips of type I collagen fibrils formed in vitro are near-paraboloidal in shape, implying a reciprocal relationship between accretion and diameter.
inferredcites →https://doi.org/10.1083/jcb.103.1.231openalex-snapshot
Extracellular compartments in tendon morphogenesis: collagen fibril, bundle, and macroaggregate formation.
inferredcites →https://doi.org/10.1083/jcb.110.4.1457openalex-snapshot
The spatial organization of Descemet's membrane-associated type IV collagen in the avian cornea.
inferredcites →https://doi.org/10.1083/jcb.99.6.2024openalex-snapshot
Extracellular compartments in matrix morphogenesis: collagen fibril, bundle, and lamellar formation by corneal fibroblasts.
inferredcites →https://doi.org/10.1111/j.1749-6632.1985.tb51159.xopenalex-snapshot
The Structure of the Chicken α2 Collagen Genea
inferredcites →https://doi.org/10.1111/j.1749-6632.1990.tb17928.xopenalex-snapshot
Collagen Fibrillogenesis in Situ
inferredcites →https://doi.org/10.1146/annurev.bi.59.070190.004201openalex-snapshot
THE FAMILY OF COLLAGEN GENES
inferredcites →https://doi.org/10.1242/dev.107.3.437openalex-snapshot
Collagen fibril bundles: a branching assembly unit in tendon morphogenesis
inferredcites →https://doi.org/10.1242/dev.115.2.383openalex-snapshot
β-D xyloside alters dermatan sulfate proteoglycan synthesis and the organization of the developing avian corneal stroma
inferredcites →https://doi.org/10.2172/7015892openalex-snapshot
Electron microscope studies

What points at this work

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

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Use of Synergistic Effect of Mechanical Stimulation and Crimped Topography to Simulate Natural Collagen Development for Tendon Engineering
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Collagen fibrillogenesis in situ: Fibril segments become long fibrils as the developing tendon matures
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Expression of type XIV collagen in developing chicken tendons: Association with assembly and growth of collagen fibrils
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Collagen
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Biotechnological Valorization of Marine Collagens
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Decorin regulates assembly of collagen fibrils and acquisition of biomechanical properties during tendon development
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Arrangement and fine structure of collagen fibrils in the decidualized mouse endometrium
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Collagen types I, III, and V constitute the thick collagen fibrils of the mouse decidua
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The pentapeptide NKISK affects collagen fibril interactions in a vertebrate tissue
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Effect of dermatan sulfate glycosaminoglycans on the quasi‐static material properties of the human medial collateral ligament
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Altered Corneal Stromal Matrix Organization is Associated with Mucopolysaccharidosis I, III and VI
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Collagen fibrils forming in developing tendon show an early and abrupt limitation in diameter at the growing tips
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Echinoderm collagen fibrils grow by surface-nucleation-and-propagation from both centers and ends
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Dependence of Tendon Multiscale Mechanics on Sample Gauge Length is Consistent with Discontinuous Collagen Fibrils
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Incorporating plasticity of the interfibrillar matrix in shear lag models is necessary to replicate the multiscale mechanics of tendon fascicles
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Ultrastructural response of tendon to excessive level or duration of tensile load supports that collagen fibrils are mechanically continuous
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Decorin expression is important for age-related changes in tendon structure and mechanical properties
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Structure–function relationships of postnatal tendon development: A parallel to healing
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Collagen V localizes to pericellular sites during tendon collagen fibrillogenesis
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inferred← citeshttps://doi.org/10.1016/s0091-679x(08)00417-2openalex-snapshot
Chapter 17 Electron Microscopy of Collagen Fibril Structure In Vitro and In Vivo Including Three-Dimensional Reconstruction
inferred← citeshttps://doi.org/10.1016/s0736-0266(00)00075-9openalex-snapshot
The effect of NKISK on tendon in an in vivo model
inferred← citeshttps://doi.org/10.1016/s0736-0266(02)00084-0openalex-snapshot
Development‐associated differences in integrative cartilage repair: Roles of biosynthesis and matrix
inferred← citeshttps://doi.org/10.1016/s0921-0423(03)80005-9openalex-snapshot
Chapter V Collagen and gelatin
inferred← citeshttps://doi.org/10.1016/s0923-1811(02)00023-3openalex-snapshot
Size control of decorin dermatan sulfate during remodeling of collagen fibrils in healing skin
inferred← citeshttps://doi.org/10.1016/s0928-4931(00)00137-5openalex-snapshot
Microstructural evolution in external callus of human long bone
inferred← citeshttps://doi.org/10.1016/s0945-053x(00)00082-2openalex-snapshot
Tip-mediated fusion involving unipolar collagen fibrils accounts for rapid fibril elongation, the occurrence of fibrillar branched networks in skin and the paucity of collagen fibril ends in vertebrates
inferred← citeshttps://doi.org/10.1016/s0945-053x(96)90152-3openalex-snapshot
Characterization of collagen fibril segments from chicken embryo cornea, dermis and tendon
inferred← citeshttps://doi.org/10.1016/s0968-4328(00)00040-8openalex-snapshot
STEM/TEM studies of collagen fibril assembly
inferred← citeshttps://doi.org/10.1016/s0968-4328(00)00042-1openalex-snapshot
Collagen structure and functional implications
inferred← citeshttps://doi.org/10.1016/s0968-4328(00)00043-3openalex-snapshot
Type V collagen: heterotypic type I/V collagen interactions in the regulation of fibril assembly
inferred← citeshttps://doi.org/10.1016/s1065-6995(03)00099-4openalex-snapshot
Cellular aspects of elastogenesis in the elastic tendon of the chicken wing
inferred← citeshttps://doi.org/10.1016/s1095-6433(02)00212-xopenalex-snapshot
Collagen fibril biosynthesis in tendon: a review and recent insights
inferred← citeshttps://doi.org/10.1016/s1440-2440(99)80173-xopenalex-snapshot
Optimisation of the biology of soft tissue repair
inferred← citeshttps://doi.org/10.1017/s1431927603030277openalex-snapshot
Analysis of Orientations of Collagen Fibers by Novel Fiber-Tracking Software
inferred← citeshttps://doi.org/10.1021/acs.biomac.1c00013openalex-snapshot
Diverse and Productive Source of Biopolymer Inspiration: Marine Collagens
inferred← citeshttps://doi.org/10.1021/acsnano.5b07756openalex-snapshot
Flow-Induced Crystallization of Collagen: A Potentially Critical Mechanism in Early Tissue Formation
inferred← citeshttps://doi.org/10.1023/a:1019896210320openalex-snapshot
Boundary conditions during biaxial testing of planar connective tissues. Part 1: Dynamic Behavior
inferred← citeshttps://doi.org/10.1038/srep31998openalex-snapshot
Nanochips of Tantalum Oxide Nanodots as artificial-microenvironments for monitoring Ovarian cancer progressiveness
inferred← citeshttps://doi.org/10.1039/9781839161124-00001openalex-snapshot
The Mutable Collagenous Tissue of Echinoderms: From Biology to Biomedical Applications
inferred← citeshttps://doi.org/10.1039/d5tb01841bopenalex-snapshot
Molecular versatility of polyproline II helices: from natural proteins to biomimetic materials
inferred← citeshttps://doi.org/10.1042/bj3160001openalex-snapshot
Collagen fibril formation
inferred← citeshttps://doi.org/10.1042/bj3170785openalex-snapshot
Differential expression of fibromodulin mRNA associated with tendon fibril growth: isolation and characterization of a chicken fibromodulin cDNA
inferred← citeshttps://doi.org/10.1046/j.1440-169x.1997.t01-4-00003.xopenalex-snapshot
Alterations in sarcomere structure, collagen organization, mitochondrial activity, and protein metabolism in the avian low score normal muscle weakness
inferred← citeshttps://doi.org/10.1046/j.1440-169x.1999.00422.xopenalex-snapshot
Myotube morphology, and expression and distribution of collagen type I during normal and low score normal avian satellite cell myogenesis
inferred← citeshttps://doi.org/10.1053/joca.2001.0502openalex-snapshot
Integrative articular cartilage repair: dependence on developmental stage and collagen metabolism
inferred← citeshttps://doi.org/10.1073/pnas.0502718103openalex-snapshot
Microfibrillar structure of type I collagen in situ
inferred← citeshttps://doi.org/10.1073/pnas.1300135110openalex-snapshot
Characterization of mechanical and biochemical properties of developing embryonic tendon
inferred← citeshttps://doi.org/10.1074/jbc.m101613200openalex-snapshot
Production of Human Type I Collagen in Yeast Reveals Unexpected New Insights into the Molecular Assembly of Collagen Trimers
inferred← citeshttps://doi.org/10.1074/jbc.m111.223693openalex-snapshot
Regulation of Collagen Fibril Nucleation and Initial Fibril Assembly Involves Coordinate Interactions with Collagens V and XI in Developing Tendon
inferred← citeshttps://doi.org/10.1074/jbc.m409622200openalex-snapshot
Type V Collagen Controls the Initiation of Collagen Fibril Assembly
inferred← citeshttps://doi.org/10.1074/jbc.m511528200openalex-snapshot
Murine Model of the Ehlers-Danlos Syndrome
inferred← citeshttps://doi.org/10.1074/jbc.m805582200openalex-snapshot
Type XIV Collagen Regulates Fibrillogenesis
inferred← citeshttps://doi.org/10.1074/jbc.m806590200openalex-snapshot
Genetic Evidence for the Coordinated Regulation of Collagen Fibrillogenesis in the Cornea by Decorin and Biglycan
inferred← citeshttps://doi.org/10.1080/02664763.2011.596193openalex-snapshot
Two-stage hierarchical modeling for analysis of subpopulations in conditional distributions
inferred← citeshttps://doi.org/10.1080/03008200490278070openalex-snapshot
Collagen Fibrillogenesis and mRNA Levels in the Maturing Rabbit Medial Collateral Ligament and Patellar Tendon
inferred← citeshttps://doi.org/10.1080/03008200490522997openalex-snapshot
Biochemical and Biomechanical Analysis of Tendons of Caged and Penned Chickens
inferred← citeshttps://doi.org/10.1080/03008200600846606openalex-snapshot
Structural Change in Decorin with Skin Aging
inferred← citeshttps://doi.org/10.1080/03008200802325250openalex-snapshot
Structural and Biochemical Analysis of the Effect of Immobilization Followed by Stretching on the Calcaneal Tendon of Rats
inferred← citeshttps://doi.org/10.1080/03008207.2017.1306059openalex-snapshot
Effect of carboxymethylcellulose on fibril formation of collagenin vitro
inferred← citeshttps://doi.org/10.1080/03008207.2018.1511710openalex-snapshot
Roadmap of molecular, compositional, and functional markers during embryonic tendon development
inferred← citeshttps://doi.org/10.1080/03008207.2024.2432324openalex-snapshot
Tendon-targeted knockout of collagen XI disrupts patellar and Achilles tendon structure and mechanical properties during murine postnatal development
inferred← citeshttps://doi.org/10.1080/15419060701755552openalex-snapshot
A Novel Subcellular Collagen Organization Process Visualized by Total Internal Reflection Fluorescence Microscopy
inferred← citeshttps://doi.org/10.1081/e-ebpp-120019340openalex-snapshot
Collagen Processing
inferred← citeshttps://doi.org/10.1083/jcb.136.3.729openalex-snapshot
Targeted Disruption of Decorin Leads to Abnormal Collagen Fibril Morphology and Skin Fragility
inferred← citeshttps://doi.org/10.1083/jcb.142.1.285openalex-snapshot
Cartilage Fibrils of Mammals are Biochemically Heterogeneous: Differential Distribution of Decorin and Collagen IX
inferred← citeshttps://doi.org/10.1083/jcb.151.4.779openalex-snapshot
Differential Expression of Lumican and Fibromodulin Regulate Collagen Fibrillogenesis in Developing Mouse Tendons
inferred← citeshttps://doi.org/10.1083/jcb.200203069openalex-snapshot
Slow local movements of collagen fibers by fibroblasts drive the rapid global self-organization of collagen gels
inferred← citeshttps://doi.org/10.1083/jcb.201108062openalex-snapshot
Matrix nanotopography as a regulator of cell function
inferred← citeshttps://doi.org/10.1089/10763270360696969openalex-snapshot
Tissue-Engineering Approach to the Repair and Regeneration of Tendons and Ligaments
inferred← citeshttps://doi.org/10.1089/ten.tea.2009.0014openalex-snapshot
Collagen-Binding Peptidoglycans: A Biomimetic Approach to Modulate Collagen Fibrillogenesis for Tissue Engineering Applications
inferred← citeshttps://doi.org/10.1089/ten.tea.2012.0347openalex-snapshot
Human Recombinant Type I Collagen Produced in Plants
inferred← citeshttps://doi.org/10.1089/ten.teb.2019.0243openalex-snapshot
Mechanical Roles in Formation of Oriented Collagen Fibers
inferred← citeshttps://doi.org/10.1089/wound.2021.0069openalex-snapshot
Small Leucine-Rich Proteoglycans in Tendon Wound Healing
inferred← citeshttps://doi.org/10.1093/ps/76.3.506openalex-snapshot
Identification of decorin and chondroitin sulfate proteoglycans in turkey skeletal muscle
inferred← citeshttps://doi.org/10.1093/ps/76.6.878openalex-snapshot
Decorin and collagen type I gene expression in avian low score normal pectoral muscle
inferred← citeshttps://doi.org/10.1093/ps/77.3.464openalex-snapshot
Transforming growth factor-beta gene expression in avian Low Score Normal pectoral muscle
inferred← citeshttps://doi.org/10.1096/fj.202501618ropenalex-snapshot
Collagen XII Plays a More Prominent Cell‐Mediated Role in Tendon Organization Compared to Matrix Assembly During Postnatal Development
inferred← citeshttps://doi.org/10.1097/01.prs.0000070180.62037.fcopenalex-snapshot
Is the Tendon Embryogenesis Process Resurrected during Tendon Healing?
inferred← citeshttps://doi.org/10.1097/brs.0b013e31805931d8openalex-snapshot
Cell Polarity in the Anulus of the Human Intervertebral Disc
inferred← citeshttps://doi.org/10.1098/rsfs.2015.0043openalex-snapshot
Collagen V-heterozygous and -null supraspinatus tendons exhibit altered dynamic mechanical behaviour at multiple hierarchical scales
inferred← citeshttps://doi.org/10.1098/rspb.2005.3173openalex-snapshot
Influence of fibril taper on the function of collagen to reinforce extracellular matrix
inferred← citeshttps://doi.org/10.1100/tsw.2007.92openalex-snapshot
Collagen Structure of Tendon Relates to Function
inferred← citeshttps://doi.org/10.1101/2023.08.25.554314openalex-snapshot
Structural Determinants of Tendon Function During Development and Their Sensitivity to Mechanical Stimulation
inferred← citeshttps://doi.org/10.1111/febs.12136openalex-snapshot
The regulatory roles of small leucine‐rich proteoglycans in extracellular matrix assembly
inferred← citeshttps://doi.org/10.1111/iep.12027openalex-snapshot
The role of the non‐collagenous matrix in tendon function
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2009.01170.xopenalex-snapshot
Collagen fibril organization in the pregnant endometrium of decorin‐deficient mice
inferred← citeshttps://doi.org/10.1111/joa.12485openalex-snapshot
Distribution of proteins within different compartments of tendon varies according to tendon type
inferred← citeshttps://doi.org/10.1111/joa.13125openalex-snapshot
Age‐related changes of tendon fibril micro‐morphology and gene expression
inferred← citeshttps://doi.org/10.1111/joa.70006openalex-snapshot
Characterisation of spinal ligaments in the embryonic chick
inferred← citeshttps://doi.org/10.1115/1.4006538openalex-snapshot
Examining Differences in Local Collagen Fiber Crimp Frequency Throughout Mechanical Testing in a Developmental Mouse Supraspinatus Tendon Model
inferred← citeshttps://doi.org/10.1115/1.4038745openalex-snapshot
Multiscale Poroviscoelastic Compressive Properties of Mouse Supraspinatus Tendons Are Altered in Young and Aged Mice
inferred← citeshttps://doi.org/10.1115/1.4066570openalex-snapshot
Regulatory Role of Collagen XI in the Establishment of Mechanical Properties of Tendons and Ligaments in Mice Is Tissue Dependent
inferred← citeshttps://doi.org/10.1128/mcb.25.2.699-705.2005openalex-snapshot
Tenomodulin Is Necessary for Tenocyte Proliferation and Tendon Maturation
inferred← citeshttps://doi.org/10.1134/s0006350907050065openalex-snapshot
Collagen type I fibril packing in vivo and in vitro
inferred← citeshttps://doi.org/10.1146/annurev-bioeng-071811-150122openalex-snapshot
Tendon Healing: Repair and Regeneration
inferred← citeshttps://doi.org/10.1146/annurev.biochem.67.1.609openalex-snapshot
MATRIX PROTEOGLYCANS: From Molecular Design to Cellular Function
inferred← citeshttps://doi.org/10.1152/japplphysiol.00328.2016openalex-snapshot
Effect of aging and exercise on the tendon
inferred← citeshttps://doi.org/10.1152/japplphysiol.00340.2002openalex-snapshot
Hindlimb unloading alters ligament healing
inferred← citeshttps://doi.org/10.1159/000063713openalex-snapshot
Decorin Expression during Development of Bovine Skeletal Muscle and Its Role in Morphogenesis of the Intramuscular Connective Tissue
inferred← citeshttps://doi.org/10.11606/d.42.2009.tde-09062009-103722openalex-snapshot
Estudo ultraestrutural e imunohistoquímico do estroma uterino durante a gestação de camundongos deficientes em decorim.
inferred← citeshttps://doi.org/10.1167/iovs.02-0783openalex-snapshot
Ocular and Scleral Alterations in Gene-Targeted Lumican-Fibromodulin Double-Null Mice
inferred← citeshttps://doi.org/10.1167/iovs.04-1253openalex-snapshot
Changes in Collagen Orientation and Distribution in Keratoconus Corneas
inferred← citeshttps://doi.org/10.1172/jci2131openalex-snapshot
Altered wound healing in mice lacking a functional osteopontin gene (spp1).
inferred← citeshttps://doi.org/10.1177/002215549904701212openalex-snapshot
Development and Aging of the Articular Cartilage of the Rabbit Knee Joint: Distribution of Biglycan, Decorin, and Matrilin-1
inferred← citeshttps://doi.org/10.1186/1472-6793-7-2openalex-snapshot
Systemic administration of IGF-I enhances healing in collagenous extracellular matrices: evaluation of loaded and unloaded ligaments
inferred← citeshttps://doi.org/10.1201/9780203909720.ch11openalex-snapshot
Corneal Proteoglycans
inferred← citeshttps://doi.org/10.1201/b13733-4openalex-snapshot
Tendon and Ligament Biomechanics
inferred← citeshttps://doi.org/10.1201/b13733-7openalex-snapshot
Musculoskeletal Structures
inferred← citeshttps://doi.org/10.1242/jcs.01731openalex-snapshot
Procollagen trafficking, processing and fibrillogenesis
inferred← citeshttps://doi.org/10.1292/jvms.67.855openalex-snapshot
Control of the Collagen Fibril Diameter in the Equine Superficial Digital Flexor Tendon in Horses by Decorin
inferred← citeshttps://doi.org/10.12935/jvma.63.38openalex-snapshot
A Preliminary Study of the Administrative Effect of Collagen Peptides Derived from Salmon Skin on Dermis Around Bovine Hooves
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