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자료유형
학술저널
저자정보
Hyun Ju Cha (Hallym University) Won Sik Eum (Hallym University) Gi Soo Youn (Hallym University) Jung Hwan Park (Hallym University) Hyeon Ji Yeo (Hallym University) Eun Ji Yeo (Hallym University) Hyun Jung Kwon (Hallym University) Lee Re Lee (Hallym University) Na Yeon Kim (Hallym University) Su Yeon Kwon (Hallym University) Yong-Jun Cho (Hallym University Medical Center) Sung-Woo Cho (University of Ulsan College of Medicine) Oh-Shin Kwon (College of Natural Sciences Kyungpook National University) Eun Jeong Sohn (Hallym University) Dae Won Kim (Gangneung-Wonju National University) Duk-Soo Kim (Soonchunhyang University) Yu Ran Lee (Soonchunhyang University) Min Jea Shin (Hallym University) Soo Young CHOI (Hallym University)
저널정보
대한생화학·분자생물학회 BMB Reports BMB Reports 제56권 제4호
발행연도
2023.4
수록면
234 - 239 (6page)

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Thioredoxin-like protein 1 (TXNL1), one of the thioredoxin superfamilyknown as redox-regulator, plays an essential in maintainingcell survival via various antioxidant and anti-apoptoticmechanisms. It is well known that relationship between ischemiaand oxidative stress, however, the role of TXNL1 protein inischemic damage has not been fully investigated. In the presentstudy, we aimed to determine the protective role of TXNL1against on ischemic injury in vitro and in vivo using cellpermeable Tat-TXNL1 fusion protein. Transduced Tat-TXNL1inhibited ROS production and cell death in H2O2-exposedhippocampal neuronal (HT-22) cells and modulated MAPKsand Akt activation, and pro-apoptotic protein expression levelsin the cells. In an ischemia animal model, Tat-TXNL1 markedlydecreased hippocampal neuronal cell death and the activationof astrocytes and microglia. These findings indicate thatcell permeable Tat-TXNL1 protects against oxidative stress invitro and in vivo ischemic animal model. Therefore, we suggestTat-TXNL1 can be a potential therapeutic protein for ischemicinjury.

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