4.4 Article

Activation of the transcription factor c-Jun in acute cellular and antibody-mediated rejection after kidney transplantation

Journal

HUMAN PATHOLOGY
Volume 41, Issue 12, Pages 1682-1693

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.humpath.2010.04.016

Keywords

c-Jun; Acute allograft rejection; Kidney transplantation; JNK

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c-Jun is a transcription factor that belongs to the activator protein-1 family of proteins In human kidney disease, c-Jun is activated in glomerular and tubular cells and plays a major role in renal pathophysiology However, the contribution of this pathway to renal allograft rejection has not been determined We investigated whether c-Jun is activated in acute allograft rejection c-Jun activation was assessed with immunohistochemistry using phospho-specific c-Jun antibodies in control human renal tissue and renal tissue from patients with acute cellular rejection, acute antibody-mediated rejection, and no rejection in the month after transplantation In patients with acute cellular rejection, c-Jun activation was observed primarily in infiltrated T cells associated with tubulitis, interstitial cell infiltration, and endarteritis The number of infiltrated phosphorylated c-Jun positive cells in the tubules and interstitium was correlated with the Banff classification t and 1 scores In patients with acute antibody-mediated rejection, c-Jun activation was observed in Injured endothelial cells as well as in infiltrated cells, including macrophages, in the glomerular and peritubular capillaries Furthermore, the serum creatinine levels and changes in serum creatinine from the previous year were significantly correlated with the total tubulointerstitial phosphorylated c-Jun-positive score (representing the number of positive nuclei in the tubules, interstitium, and peritubular capillaries) In conclusion, c-Jun was activated in acute antibody-mediated rejection and acute cellular rejection and was associated with reduced graft function These findings suggest that c-Jun plays a key role in pathological events and may represent a novel therapeutic target in acute renal allograft rejection (C) 2010 Elsevier Inc All rights reserved

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