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Role of the Tau N-terminal region in microtubule stabilization revealed by new endogenous truncated forms.
Derisbourg, Maxime; Leghay, Coline; Chiappetta, Giovanni; Fernandez-Gomez, Francisco-Jose; Laurent, Cyril; Demeyer, Dominique; Carrier, Sébastien; Buée-Scherrer, Valérie; Blum, David; Vinh, Joëlle; Sergeant, Nicolas; Verdier, Yann; Buée, Luc; Hamdane, Malika.
Afiliación
  • Derisbourg M; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Leghay C; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Chiappetta G; ESPCI Biological Mass Spectrometry and Proteomics USR 3149 CNRS/ESPCI ParisTech, Paris, France.
  • Fernandez-Gomez FJ; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France.
  • Laurent C; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France.
  • Demeyer D; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Carrier S; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Buée-Scherrer V; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Blum D; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Vinh J; ESPCI Biological Mass Spectrometry and Proteomics USR 3149 CNRS/ESPCI ParisTech, Paris, France.
  • Sergeant N; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Verdier Y; ESPCI Biological Mass Spectrometry and Proteomics USR 3149 CNRS/ESPCI ParisTech, Paris, France.
  • Buée L; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
  • Hamdane M; 1] Inserm, UMR-S 1172, Alzheimer &Tauopathies, Jean-Pierre Aubert Research Centre, Faculté de Médecine, IMPRT, F-59045, Lille, France [2] Université de Lille, F-59045, Lille, France [3] CHRU-Lille, F-59037, Lille, France.
Sci Rep ; 5: 9659, 2015 May 14.
Article en En | MEDLINE | ID: mdl-25974414
Tau is a central player in Alzheimer's disease (AD) and related Tauopathies, where it is found as aggregates in degenerating neurons. Abnormal post-translational modifications, such as truncation, are likely involved in the pathological process. A major step forward in understanding the role of Tau truncation would be to identify the precise cleavage sites of the several truncated Tau fragments that are observed until now in AD brains, especially those truncated at the N-terminus, which are less characterized than those truncated at the C-terminus. Here, we optimized a proteomics approach and succeeded in identifying a number of new N-terminally truncated Tau species from the human brain. We initiated cell-based functional studies by analyzing the biochemical characteristics of two N-terminally truncated Tau species starting at residues Met11 and Gln124 respectively. Our results show, interestingly, that the Gln124-Tau fragment displays a stronger ability to bind and stabilize microtubules, suggesting that the Tau N-terminal domain could play a direct role in the regulation of microtubule stabilization. Future studies based on our new N-terminally truncated-Tau species should improve our knowledge of the role of truncation in Tau biology as well as in the AD pathological process.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tubulina (Proteína) / Proteínas tau / Enfermedad de Alzheimer / Microtúbulos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2015 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tubulina (Proteína) / Proteínas tau / Enfermedad de Alzheimer / Microtúbulos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2015 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido