Signal transduction pathway of p66shc through -amyloid peptides

Increased oxidative stress is the leading mechanism of Abeta induced cell death. P66Shc, the growth factor adaptor protein has been implicated as a major regulator of reactive oxygen species (ROS) production hence apoptotic signalling cascade. Accordingly, better understanding of p66Shc signalling pathway through the mediation of Abeta may provide clues as to how to protect brain cells from the toxic effects of Abeta. Abeta leads to progressive cell death in a concentration dependent manner. Abeta phosphorylates p66Shc at S36 residue in a dose dependent and time dependent application of Abeta. Similarly, Abeta mediates the activation of MKK6 by mediating phosphorylation at S207 residue at the same concentrations and time points. Ectopic expression of p66ShcS36A and MKK6 (TM) protected cells against Abeta induced death, suggesting that p66Shc and MKK6 phosphorylation critically influences the toxicity of C6 cells induced by Abeta. Finally, ROS scavengers and knock-down against p66Shc and MKK6 significantly decreased ROS production and cell death.

Autorentext

A Dra. Muneesa Bashir é doutorada em Biotecnologia pela Universidade de Caxemira, Índia. Atualmente trabalha como Professora Assistente, Biotecnologia, Departamento de Ensino Superior, JK, Índia. Tem cerca de 6 artigos de investigação publicados em revistas internacionais de renome.

Klappentext

Increased oxidative stress is the leading mechanism of Aß induced cell death. P66Shc, the growth factor adaptor protein has been implicated as a major regulator of reactive oxygen species (ROS) production hence apoptotic signalling cascade. Accordingly, better understanding of p66Shc signalling pathway through the mediation of Aß may provide clues as to how to protect brain cells from the toxic effects of Aß. Aß leads to progressive cell death in a concentration dependent manner. Aß phosphorylates p66Shc at S36 residue in a dose dependent and time dependent application of Aß. Similarly, Aß mediates the activation of MKK6 by mediating phosphorylation at S207 residue at the same concentrations and time points. Ectopic expression of p66ShcS36A and MKK6 (TM) protected cells against Aß induced death, suggesting that p66Shc and MKK6 phosphorylation critically influences the toxicity of C6 cells induced by Aß. Finally, ROS scavengers and knock-down against p66Shc and MKK6 significantly decreased ROS production and cell death.