Laminin assembles into separate basement membrane and fibrillar matrices in Schwann cells

Journal of Cell Science

Volumn 115, Issue 5, 2002, Pages 1005-1015

  Tsiper, Maria V ^a   Yurchenco, Peter D ^a  

^a RUTGERS ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

Author keywords

Collagen; Dystroglycan; Integrin; Laminin; Schwann cell; Utrophin

Indexed keywords

BETA1 INTEGRIN; BLOCKING ANTIBODY; CELL RECEPTOR; COLLAGEN TYPE 4; DYSTROGLYCAN; HEPARIN; LAMININ; LAMININ 1; MEROSIN; PEPTIDE FRAGMENT; UTROPHIN;

ANIMAL CELL; ARTICLE; BASEMENT MEMBRANE; CELL ANCHORAGE; CELL FUNCTION; CELL MEMBRANE; CELL STRUCTURE; CELL SURFACE; CELL ULTRASTRUCTURE; COMPLEX FORMATION; CONTROLLED STUDY; CYTOSKELETON; EXTRACELLULAR MATRIX; NERVE FIBER; NEUROMUSCULAR SYSTEM; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN POLYMERIZATION; RAT; RETICULUM CELL; SCHWANN CELL;

ANIMALS; ANIMALS, NEWBORN; AXONS; BASEMENT MEMBRANE; CELLS, CULTURED; COLLAGEN TYPE IV; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; EXTRACELLULAR MATRIX; LAMININ; MEMBRANE GLYCOPROTEINS; MICROSCOPY, ELECTRON; POLYMERS; PROTEIN BINDING; RATS; RATS, SPRAGUE-DAWLEY; RETICULIN; SCHWANN CELLS;

ANIMALIA;

EID: 0036500536     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (44)

1. Skin and hair follicle integrity is crucially dependent on beta1 integrin expression on keratinocytes
2. Neuron-Schwann cell interaction in basal lamina formation
3. Self-assembly of laminin isoforms
4. Schwann cell extracellular matrix molecules and their receptors
5. Schwann cells use a novel collagen-dependent mechanism for fibronectin fibril assembly
6. Cultured Schwann cells assemble normal-appearing basal lamina only when they ensheathe axons
7. The laminin alpha2 expressed by dystrophic dy(2J) mice is defective in its ability to form polymers
8. Form and function: The laminin family of heterotrimers
9. The laminin alpha2-chain short arm mediates cell adhesion through both the alpha1beta1 and alpha2beta1 integrins
10. Laminin polymerization induces a receptor-cytoskeleton network
11. Chimeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses
12. alpha3beta1 integrin is required for normal development of the epidermal basement membrane
13. Axonal regulation of Schwann cell integrin expression suggests a role for alpha 6 beta 4 in myelination
14. Anti-beta 1 integrin antibody inhibits Schwann cell myelination
15. Regulation of the fibronectin receptor affinity by divalent cations
16. Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: From identification of mutations to prenatal diagnosis
17. Dystroglycan: A extracellular matrix receptor linked to the cytoskeleton
18. A role for dystroglycan in basement membrane assembly
19. Basement membranes during development of human nerve: Schwann cells and perineurial cells display marked changes in their expression profiles for laminin subunits and beta 1 and beta 4 integrins
20. Control of extracellular matrix assembly by syndecan-2 proteoglycan
21. Merosin-deficient Congenital Muscular Dystrophy. Partial genetic correction in two mouse models
22. Assembly of laminin polymers is dependent on beta1-integrins
23. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse
24. Differential heparin inhibition of skeletal muscle alpha-dystroglycan binding to laminins
25. Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice
26. Laminin binds specifically to sulfated glycolipids
27. Deficiency of beta 1 integrins in teratoma interferes with basement membrane assembly and laminin-1 expression
28. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy
29. Laminin receptor on platelets is the integrin VLA-6
30. Expression and regulation of alpha1beta1 integrin in Schwann cells
31. Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice
32. Localization of heparin binding activity in recombinant laminin G domain
33. Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins
34. Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin
35. Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene
36. Characterization of dystroglycan-laminin interaction in peripheral nerve
37. Assembly of laminin and type IV collagen into basement membrane networks
38. Self-assembly and calcium-binding sites in laminin. A three-arm interaction model
39. Self-assembly of basement membrane collagen
40. Basement membrane assembly
41. Laminin forms an independent network in basement membranes
42. Recombinant laminin G domain mediates myoblast adhesion and heparin binding
43. The alpha chain of laminin-1 is independently secreted and drives secretion of its beta- and gamma-chain partners
44. Rho-mediated contractility exposes a cryptic site in fibronectin and induces fibronectin matrix assembly