| Literature DB >> 34498916 |
Yubin Wang1, James Brazdzionis2, Fanglong Dong1, Tye Patchana2, Hammad Ghanchi2, Stacey Podkovik2, James G Wiginton2, Maxwell Marino2, Jason Duong3, Margaret Wacker3, Dan E Miulli3, Michael Neeki3, Xiaoning Bi1, Michel Baudry1.
Abstract
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.Entities:
Keywords: PTPN13; blood biomarker; calpain; traumatic brain injury
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Year: 2021 PMID: 34498916 DOI: 10.1089/neu.2021.0229
Source DB: PubMed Journal: J Neurotrauma ISSN: 0897-7151 Impact factor: 5.269