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PMID:11456309

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Citation

Nobbio, L, Mancardi, G, Grandis, M, Levi, G, Suter, U, Nave, KA, Windebank, AJ, Abbruzzese, M and Schenone, A (2001) PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. Ann. Neurol. 50:47-55

Abstract

Charcot-Marie-Tooth 1A (CMT1A) neuropathy is caused by duplication of the peripheral myelin protein 22 (PMP22) gene, leading to protein overexpression. Although this protein has a role in regulating Schwann cell growth and peripheral myelin compaction, how altered concentrations of PMP22 impair myelination is unknown. We established dorsal root ganglia (DRG) cultures from a transgenic rat overexpressing PMP22 (PMP22tg) to study the behavior of PMP22tg Schwann cells in early stages of development and myelination. We used reverse transcriptase-polymerase chain reaction and light and electron microscopy to study PMP22 expression and myelin formation. Myelin ultrastructure was evaluated in sural nerves from CMT1A patients to compare experimental and human findings. PMP22tg DRG cultures contained a greater number of internodes devoid of myelin, in the absence of remyelination, and increased periodicity of myelin lamellae compared with normal cultures. Widening of myelin lamellae was also observed in CMT1A biopsy specimens. Our results suggest that both functions of PMP22, in regulating Schwann cell differentiation and contributing to peripheral myelin compaction, are affected by its overexpression. The presence of similar myelin abnormalities in PMP22tg cultures and human nerves emphasizes the importance of developing in vitro models of hereditary neuropathies to study their underlying pathomechanisms.

Links

PubMed

Keywords

Animals; Animals, Genetically Modified; Cell Culture Techniques; Ganglia, Spinal/metabolism; Ganglia, Spinal/ultrasonography; Humans; Male; Microscopy, Electron; Myelin Proteins/genetics; Myelin Proteins/metabolism; Myelin Sheath/metabolism; RNA, Messenger/metabolism; Rats; Rats, Sprague-Dawley/genetics; Sural Nerve/ultrastructure; Tetracycline/metabolism

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

RAT:PMP22

involved_in

GO:0030154: cell differentiation

ECO:0000314: direct assay evidence used in manual assertion

P

Seeded From UniProt

complete

RAT:PMP22

involved_in

GO:0042552: myelination

ECO:0000314: direct assay evidence used in manual assertion

P

Seeded From UniProt

complete

RAT:PMP22

involved_in

GO:0042552: myelination

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete


See also

References

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