Function of tetraspan proteins in the myelin sheath

Current Opinion in Neurobiology

Volumn 10, Issue 5, 2000, Pages 552-557

  Bronstein, Jeff M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32; MYELIN PROTEIN; PROTEOLIPID PROTEIN;

CELL ADHESION; CELL MEMBRANE TRANSPORT; CELL MIGRATION; GROWTH REGULATION; HUMAN; MYELIN SHEATH; NONHUMAN; OLIGODENDROGLIA; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; REVIEW; SCHWANN CELL;

EID: 0033739691     PISSN: 09594388     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-4388(00)00125-2     Document Type: Review

References (59)

1. Redefining the lipophilin family of proteolipid proteins
2. Oligodendrocyte-specific protein (OSP) is a major component of CNS myelin
3. Identification of a new exon in the myelin proteolipid protein gene encoding novel protein isoforms that are restricted to the somata of oligodendrocytes and neurons
4. Assembly of CNS myelin in the absence of proteolipid protein
5. Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice
6. Proteolipid protein is necessary in peripheral as well as central myelin
7. Peripheral neuropathy caused by proteolipid protein gene mutations
8. Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage
9. Distinct phenotypes associated with increasing dosage of the PLP gene: Implications for CMT1A due to PMP22 gene duplication
10. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease
11. Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: Molecular mechanism and phenotypic manifestations
12. Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2)
13. The molecular pathogenesis of Pelizaeus-Merzbacher disease
14. Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease
15. Pelizaeus-Merzbacher disease: X-linked proteolipid protein deficiency in human central nervous system
16. PMP-22 expression in the central nervous system of the embryonic mouse defines potential transverse segments and longitudinal columns
17. Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
18. The peripheral myelin protein 22 and epithelial membrane protein family
19. Involvement of OSP/claudin-11 in oligodendrocyte membrane interactions: Role in biology and disease
20. SEMP1, a senescence-associated cDNA isolated from human mammary epithelial cells, is a member of an epithelial membrane protein superfamily
21. Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth
22. Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines
23. Immunoreactivity of PMP-22, PO, and other 19 to 28 kDa glycoproteins in peripheral nerve myelin of mammals and fish with HNK1 and related antibodies
24. Peripheral myelin protein 22 and protein zero: A novel association in peripheral nervous system myelin
25. Tetraspan myelin protein PMP22 and demyelinating peripheral neuropathies: New facts and hypotheses
26. Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients
27. Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): Normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs
28. A transgenic rat model of Charcot-Marie-Tooth disease
29. Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage
30. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
31. Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22
32. Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies
33. Isolation and characterization of a novel oligodendrocyte-specific protein
34. Developmental expression of OSP/claudin-11
35. Claudin-11/OSP-based tight junctions of myelin sheaths in brain and sertoli cells in testis
36. CNS myelin and sertoli cell tight junction strands are absent in Osp/claudin-11 null mice
37. Chromosomal localization of murine and human oligodendrocyte-specific protein genes
38. The tight junction: Morphology to molecules
39. Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin
40. Occludin-deficient embryonic stem cells can differentiate into polarized epithelial cells bearing tight junctions
41. Structural and signalling molecules come together at tight junctions
42. Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption
43. Characterization of a rat gene, rMAL, encoding a protein with four hydrophobic domains in central and peripheral myelin
44. Myelin and lymphocyte protein (MAL/MVP17/VIP17) and plasmolipin are members of an extended gene family
45. Assignment of the T-cell differentiation gene MAL to human chromosome 2, region cen-q13
46. Developmental expression pattern of the myelin proteolipid MAL indicates different functions of MAL for immature Schwann cells and in a late step of CNS myelinogenesis
47. MAL, a proteolipid in glycosphingolipid enriched domains: Functional implications in myelin and beyond
48. VIP17/MAL, a lipid raft-associated protein, is involved in apical transport in MDCK cells
49. The role of the gap junction protein connexin32 in the myelin sheath
50. Connexin32 is a myelin-related protein in the PNS and CNS
51. Functional gap junctions in the Schwann cell myelin sheath
52. Putative gap junctional communication between axon and regenerating Schwann cells during mammalian peripheral nerve regeneration
53. Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice
54. The tetraspanin superfamily: Molecular facilitators
55. Sequences and expression of six new members of the tetraspanin/TM4SF family
56. Sequence and expression of seven new tetraspans
57. An antibody to the tetraspan membrane protein CD9 promotes neurite formation in a partially alpha3beta1 integrin-dependent manner
58. A novel rat tetraspan protein in cells of the oligodendrocyte lineage
59. The evolution of lipophilin genes from invertebrates to tetrapods: DM-20 cannot replace proteolipid protein in CNS myelin