卡尔帕因
创伤性脑损伤
神经保护
生物标志物
神经退行性变
医学
神经学
神经科学
药理学
疾病
病理
生物
精神科
生物化学
酶
作者
Yubin Wang,James Brazdzionis,Fanglong Dong,Tye Patchana,Hammad Ghanchi,Stacey Podkovik,James Wiginton,Maxwell A Marino,Jason Duong,Margaret Rose Wacker,Dan E Miulli,Michael Neeki,Xiaoning Bi,Michel Baudry
标识
DOI:10.1089/neu.2021.0229
摘要
Biomarkers play an increasing role in medicinal biology. They are used for diagnosis, management, drug target identification, drug responses, and disease prognosis. We have discovered that calpain-1 and calpain-2 play opposite functions in neurodegeneration, with calpain-1 activation being neuroprotective, while prolonged calpain-2 activation is neurodegenerative. This notion has been validated in several mouse models of acute neuronal injury, in particular in mouse models of traumatic brain injury (TBI) and repeated concussions. We have identified a selective substrate of calpain-2, the tyrosine phosphatase, PTPN13, which is cleaved in brain after TBI. One of the fragments generated by calpain-2, referred to as P13BP, is also found in the blood after TBI both in mice and humans. In humans, P13BP blood levels are significantly correlated with the severity of TBI, as measured by Glasgow Coma Scale scores and loss of consciousness. The results indicate that P13BP represents a novel blood biomarker for TBI.
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