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DOI 10.1093/hmg/ddu066

Медицинская библиотека · Human molecular genetics · 2014

Paeoniflorin eliminates a mutant AR via NF-YA-dependent proteolysis in spinal and bulbar muscular atrophy.

Tohnai Genki, Adachi Hiroaki, Katsuno Masahisa, Doi Hideki, Matsumoto Shinjiro, Kondo Naohide, Miyazaki Yu, Iida Madoka, Nakatsuji Hideaki, Qiang Qiang, Ding Ying, Watanabe Hirohisa, Yamamoto Masahiko, Ohtsuka Kenzo, Sobue Gen

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The accumulation of abnormal proteins is a common characteristic of neurodegenerative diseases. This accumulation reflects a severe disturbance of cellular homeostasis in pathogenic protein clearance. Here, we demonstrated that the activation of the two major proteolytic machineries, the molecular chaperone-ubiquitin proteasome system (UPS) and the autophagy system, were simultaneously enhanced by paeoniflorin (PF), a major component of Paeonia plants, and exerted therapeutic effects in models of spinal and bulbar muscular atrophy (SBMA). PF significantly increased the expression of nuclear factor-YA (NF-YA), which strongly upregulated the molecules involved in the proteolytic machinery [molecular chaperones, carboxyl terminus of Hsc70-interacting protein and transcription factor EB], which thus mitigated the behavioral and pathological impairments in an SBMA mouse model through the upregulation of pathogenic androgen receptor protein clearance in motor neurons and muscles. These findings demonstrated that PF is able to enhance both the UPS and autophagy systems by upregulating the expression of NF-YA, which promotes therapeutic effects in an SBMA model.

Для цитирования: Tohnai Genki, Adachi Hiroaki, Katsuno Masahisa, Doi Hideki, Matsumoto Shinjiro, Kondo Naohide, Miyazaki Yu, Iida Madoka, Nakatsuji Hideaki, Qiang Qiang, Ding Ying, Watanabe Hirohisa, Yamamoto Masahiko, Ohtsuka Kenzo, Sobue Gen. Paeoniflorin eliminates a mutant AR via NF-YA-dependent proteolysis in spinal and bulbar muscular atrophy.. Human molecular genetics. 2014. DOI: 10.1093/hmg/ddu066.

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