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In brain death, cerebral injury contributes to systemic biological dysregulation, causing significant cellular stress in donor kidneys adversely impacting the quality of grafts. Here, we hypothesized that DBD kidneys undergo proteolytic processes that may deem grafts susceptible to post-transplant dysfunction. Using mass spectrometry and immunoblotting, we mapped degradation profiles of cytoskeletal proteins in deceased and living donor kidney biopsies. We found that key cytoskeletal proteins in DBD kidneys were proteolytically cleaved, generating peptide fragments, predominantly in grafts with suboptimal posttransplant function. Interestingly, α-actinin-4 and Talin-1 proteolytic fragments were detected in brain-death but not in circulatory-death or living-donor kidneys with similar donor characteristics. As Talin-1 is a specific proteolytic target of Calpain-1, we investigated a potential trigger of Calpain activation and Talin-1 degradation using human ex-vivo precision-cut kidney slices and in-vitro podocytes. Notably, we showed that activation of Calpain-1 by Transforming-Growth Factor-β generated proteolytic fragments of Talin-1 that matched the degradation fragments detected in DBD preimplantation kidneys, also causing dysregulation of the actin cytoskeleton in human podocytes; events that were reversed by Calpain-1 inhibition. Our data provide initial evidence that brain death donor kidneys are more susceptible to cytoskeletal protein degradation. Correlation to posttransplant outcomes may be established by future studies.

Original publication




Journal article


Am J Transplant

Publication Date