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HERC1 Ubiquitin Ligase Is Required for Normal Axonal Myelination in the Peripheral Nervous System
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- المؤلفون: Universidad de Sevilla. Departamento de Bioquímica y Biología Molecular; Universidad de Sevilla. Departamento de Fisiología Médica y Biofísica; Dirección General de Investigación Científica y Técnica (DGICYT). España; Fundación Ramón Areces; Ministerio de Economía y Competitividad (MINECO). España; Junta de Andalucía; Bachiller, Sara; Roca Ceballos, María Angustias; García Domínguez, Irene; Pérez Villegas, Eva María; Martos Carmona, David; Pérez Castro, Miguel Ángel; Real Navarrete, Luis Miguel; Rosa, José Luis; Tabares, Lucía; Venero Recio, José Luis; Armengol, José Ángel; Carrión, Ángel Manuel; Ruiz Laza, Rocío
- نوع التسجيلة:
Electronic Resource
- الدخول الالكتروني :
https://hdl.handle.net/11441/155144
Molecular Neurobiology, 55 (112), 8856-8868.
BFU2011-27207
BFU2015-64536-R
SAF2015-64171-R
C-0009-2015
https://dx.doi.org/10.1007/s12035-018-1021-0
- معلومة اضافية
- Publisher Information:
Springer 2018-03-30
- نبذة مختصرة :
A missense mutation in HERC1 provokes loss of cerebellar Purkinje cells, tremor, and unstable gait in tambaleante (tbl) mice. Recently, we have shown that before cerebellar degeneration takes place, the tbl mouse suffers from a reduction in the number of vesicles available for release at the neuromuscular junction (NMJ). The aim of the present work was to study to which extent the alteration in HERC1 may affect other cells in the nervous system and how this may influence the motor dysfunction observed in these mice. The functional analysis showed a consistent delay in the propagation of the action potential in mutant mice in comparison with control littermates. Morphological analyses of glial cells in motor axons revealed signs of compact myelin damage as tomacula and local hypermyelination foci. Moreover, we observed an alteration in non-myelinated terminal Schwann cells at the level of the NMJ. Additionally, we found a significant increment of phosphorylated Akt-2 in the sciatic nerve. Based on these findings, we propose a molecular model that could explain how mutated HERC1 in tbl mice affects the myelination process in the peripheral nervous system. Finally, since the myelin abnormalities found in tbl mice are histological hallmarks of neuropathic periphery diseases, tbl mutant mice could be considered as a new mouse model for this type of diseases.
- الموضوع:
- Availability:
Open access content. Open access content
info:eu-repo/semantics/openAccess
- Note:
English
- Other Numbers:
SUE oai:idus.us.es:11441/155144
Bachiller, S., Roca Ceballos, M.A., García Domínguez, I., Pérez Villegas, E.M., Martos Carmona, D., Pérez Castro, M.Á.,...,Ruiz Laza, R. (2018). HERC1 Ubiquitin Ligase Is Required for Normal Axonal Myelination in the Peripheral Nervous System. Molecular Neurobiology, 55 (112), 8856-8868. https://doi.org/10.1007/s12035-018-1021-0.
0893-7648
1559-1182
10.1007/s12035-018-1021-0
1457930672
- Contributing Source:
UNIV DE SEVILLA
From OAIster®, provided by the OCLC Cooperative.
- الرقم المعرف:
edsoai.on1457930672
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