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KMID : 0620920170490050012
Experimental & Molecular Medicine
2017 Volume.49 No. 5 p.12 ~ p.12
Transcriptome analyses of chronic traumatic encephalopathy show alterations in protein phosphatase expression associated with tauopathy
Seo Jeong-Sun

Lee Seung-Bok
Shin Jong-Yeon
Hwang Yu-Jin
Cho Hye-Sun
Yoo Seong-Keun
Kim Yun-Ha
Lim Sung-Su
Kim Yun-Kyung
Hwang Eun-Mi
Kim Su-Hyun
Kim Chong-Hyun
Hyeon Seung-Jae
Yun Ji-Young
Kim Ji-Hye
Kim Yo-Na
Alvarez Victor E
Stein Thor D
Lee Jung-Hee
Kim Dong-Jin
Kim Dong-Il
Kowall Neil W
Ryu Hoon
McKee Ann C
Abstract
Chronic traumatic encephalopathy (CTE) is a progressive neurodegenerative disorder that is associated with repetitive head injury and has distinctive neuropathological features that differentiate this disease from other neurodegenerative diseases. Intraneuronal tau aggregates, although they occur in different patterns, are diagnostic neuropathological features of CTE, but the precise mechanism of tauopathy is not known in CTE. We performed whole RNA sequencing analysis of post-mortem brain tissue from patients with CTE and compared the results to normal controls to determine the transcriptome signature changes associated with CTE. The results showed that the genes related to the MAP kinase and calcium-signaling pathways were significantly downregulated in CTE. The altered expression of protein phosphatases (PPs) in these networks further suggested that the tauopathy observed in CTE involves common pathological mechanisms similar to Alzheimer¡¯s disease (AD). Using cell lines and animal models, we also showed that reduced PPP3CA/PP2B phosphatase activity is directly associated with increases in phosphorylated (p)-tau proteins. These findings provide important insights into PP-dependent neurodegeneration and may lead to novel therapeutic approaches to reduce the tauopathy associated with CTE.
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