Type V collagen: Heterotypic type I/V collagen interactions in the regulation of fibril assembly

Micron

Volumn 32, Issue 3, 2001, Pages 223-237

  Birk, D E ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

Collagen fibril; Cornea; Development; Fibril formation; Matrix assembly; Regulation of fibril assembly; Type V collagen

Indexed keywords

ALPHA HELIX; BIOLOGICAL FUNCTIONS; COLLAGEN TYPE 5; CORNEA; FIBRIL; GENETIC REGULATION; GROWTH; ISOFORM; PROTEIN DOMAIN; TISSUE DISTRIBUTION; TISSUE SPECIFICITY; TYROSINE;

COLLAGEN; CORNEA; GENE EXPRESSION REGULATION; HUMANS; MICROSCOPY, ELECTRON; PROTEIN STRUCTURE, TERTIARY;

EID: 0035219340     PISSN: 09684328     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-4328(00)00043-3     Document Type: Review

References (71)

1. In vitro formation of hybrid fibrils of type V collagen and type I collagen. Limited growth of type I collagen into thick fibrils by type V collagen
2. Targeted mutation in the co15a2 gene reveals a regulatory role for type V collagen during matrix assembly
3. Collagen fibril assembly, depostion, and organization into tissue-specific matrices
4. Localization of collagen types I, III and V during tendon development. Changes in collagen types I and III are correlated with changes in fibril diameter
5. Collagen type I and type V are present in the same fibril in the avian corneal stroma
6. Collagen fibrillogenesis in situ: Fibril segments are intermediates in matrix assembly
7. Collagen fibrillogenesis in vitro: Interaction of types I and V collagen regulates fibril diameter
8. Collagen fibrillogenesis in situ. Discontinuous segmental assembly in extracellular compartments
9. Collagen fibrillogenesis in situ: Fibril segments undergo post-depositional modifications resulting in linear and lateral growth during matrix development
10. Characterization of fibril segments from chicken embryo cornea, dermis and tendon
11. Collagen fibrillogenesis in situ: Fibril segments become long fibrils as the developing tendon matures
12. Characterization of the tissue form of type V collagen from chick bone
13. The gene encoding collagen 1(V) (COL5A1) is linked to mixed Ehlers-Danlos syndrome type I/II
14. Lumican regulates collagen fibril assembly: Skin fragility and corneal opacity in the absence of lumican
15. Targeted disruption of decorin leads to abnormal collagen fibril morphology and skin fragility
16. Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II
17. Type XII collagen is expressed in embryonic chick tendons
18. Type XIV collagen, a new homotrimeric molecule extracted from fetal bovine skin and tendon, with a triple helical disulfide-bonded domain homologous to type IX and XII collagens
19. Intracellular transport and tyrosine sulfation of procollagens V
20. Tyrosine sulfation in precursors of collagen V
21. Another look at collagen V and XI molecules
22. Organization of collagen types I and V in the embryonic chicken cornea: Monoclonal antibody studies
23. Corneal collagen fibrils: Dissection with specific collagenases and monoclonal antibodies
24. Type I and Type III collagen interactions during fibrillogenesis
25. Assembly of cartilage collagen fibrils is disrupted by overexpression of normal type II collagen in transgenic mice
26. Type V collagen and Bowman's membrane: Quantitation of mRNA in epithelium and stroma
27. Covalent crosslinking between molecules of type I and type III collagen
28. The biology of the small leucine-rich proteoglycans. Functional network of interactive proteins
29. Collagen fibril formation
30. Type III collagen can be present on banded collagen fibrils regardless of fibril diameter
31. Two type XII-like collagens localize to the surface of banded collagen fibrils
32. The human rhabdomyosarcoma cell line A204 lays down a highly insoluble matrix composed mainly of alpha 1 type-XI and alpha 2 type-V collagen chains
33. Fetal response to injury in the rabbit
34. A fibrillar collagen gene, COL11A1, is essential for skeletal morphogenesis
35. Collagen
36. Heterotypic collagen fibrils and stabilizing collagens. Controlling elements in corneal morphogenesis?
37. Development and roles of collagenous matrices in the embryonic avian cornea
38. Type V collagen: Molecular structure and fibrillar organization of the chicken alpha 1(V) NH2-terminal domain, a putative regulator of corneal fibrillogenesis
39. Type V collagens of the human placenta: Trimer alpha-chain composition, ultrastructural morphology and peptide analysis
40. Polymorphism of sickle cell hemoglobin aggregates: Structural basis for limited radial growth
41. Reduction of type V collagen using a dominant-negative strategy alters the regulation of fibrillogenesis and results in the loss of corneal-specific fibril morphology
42. New members of the collagen superfamily
43. Isolation and characterization of the chains of type V/type XI collagen present in bovine vitreous
44. Characterization of type V/XI collagen present in the embryonic chick tendon
45. Type V collagen synthesis and deposition by chicken embryo corneal fibroblasts in vitro
46. Cartilage contains mixed fibrils of collagen types II, IX, and XI
47. Mutations of the alpha2(V) chain of type V collagen impair matrix assembly and produce ehlers-danlos syndrome type I
48. Type V collagen in human amnion is a 12 nm fibrillar component of the pericellular interstitium
49. An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome
50. Identification of the cartilage alpha 1(XI) chain in type V collagen from bovine bone
51. Human placenta type V collagens. Evidence for the existence of an alpha 1(V) alpha 2(V) alpha 3(V) collagen molecule
52. Alternative exon splicing within the amino-terminal nontriple-helical domain of the rat pro-alpha 1(XI) collagen chain generates multiple forms of the mRNA transcript which exhibit tissue-dependent variation
53. Enzymes converting procollagens to collagens
54. Ultrastructural organization of type XI collagen in fetal bovine epiphyseal cartilage
55. Collagens: Molecular biology, diseases, and potentials for therapy
56. Differences in the microfibrillar arrangement of collagen fibrils. Distribution and possible significance
57. Copolymerization of pNcollagen III and collagen I. pNcollagen III decreases the rate of incorporation of collagen I into fibrils, the amount of collagen I incorporated, and the diameter of the fibrils formed
58. Collagen fibrils with straight and helicoidal microfibrils: A freeze-fracture and thin-section study
59. Characterization of a novel collagen chain in human placenta and its relation to AB collagen
60. Alternatively spliced type II procollagen mRNAs define distinct populations of cells during vertebral development: Differential expression of the amino-propeptide
61. Proteoglycan-fibrillar collagen interactions
62. FACIT collagens: Diverse molecular bridges in extracellular matrices
63. Biosynthesis of collagen crosslinks: Increased activity of purified lysyl oxidase with reconstituted fibrils
64. Molecular structure of collagen in solution: Comparison of types I, II, III and V
65. Fibromodulin-null mice have abnormal collagen fibrils, tissue organization, and altered lumican deposition in tendon
66. Differential expression of an acidic domain in the amino-terminal propeptide of mouse pro-(2(XI) collagen by complex alternative splicing
67. Glycosaminoglycans and proteoglycans
68. Tissue-specific expression of the fibril-associated collagens XII and XIV
69. Twisting of fibrin fibers limits their radial growth
70. Mutations in the COL1A2 gene of type I collagen that result in nonlethal forms of osteogenesis in perfecta
71. Expression of type XIV collagen in developing chicken tendons: Association with assembly and growth of collagen fibrils