Knockout of phosphatidylethanolamine binding protein4 (PEBP4) promotes chronic non‐bacterial prostatitis by mediating the activation of NF‐κB signaling

Abstract

AbstractBackgroundThe etiology of chronic prostatitis remains unclear; consequently, this disease is associated with recurrence and ineffective clinical therapy. Therefore, there is an urgent need to investigate the underlying pathogenesis of chronic prostatitis in order to develop more efficacious treatments.ObjectiveThe previous study found that knocking out of PEBP4 leads to chronic prostatitis in the male mice. This research aimed to identify the role of PEBP4 in prostatitis, determine the molecular pathogenic mechanisms associated with chronic prostatitis, and provide guidelines for the development of new treatment strategies for chronic prostatitis.Materials and methodsA PEBP4 exon knockout strain (PEBP4−/−) was established in C57BL/6 mice via the Cre‐loxP system. Hematoxylin‐eosin (H&E) staining was used to investigate histological changes. RNA‐sequencing was used to investigate the gene expression signature of the prostate and the levels of inflammatory cytokines were determined by real‐time polymerase chain reaction (RT‐PCR). The expression of PEBP4 protein in prostate tissue was determined by immunohistochemistry in specimens from patients with BPH and BPH combined with chronic prostatitis. Finally, we used a CRISPR‐Cas9 plasmid to knockout PEBP4 in RWPE‐1 cells; western blotting was subsequently used to measure the level of activation in the NF‐κB signaling pathway after activating with TNF‐α.ResultsHemorrhage and inflammatory cell infiltration were incidentally observed in the seminal vesicles and prostate glands of PEBP4−/− mice after being fed with a normal diet for 1 year. In addition, we found significantly lower (p < 0.001) expression levels of PEBP4 protein in prostate tissues from patients with benign prostate hyperplasia (BPH) and chronic and non‐bacterial prostatitis (CNP) when compared to those with BPH only. The reduced expression of PEBP4 led to a higher risk of prostatitis recurrence in patients after 2 years of follow‐up. Increased levels of NF‐κB and IκB phosphorylation were observed in PEBP4‐knockout RWPE‐1 cells and prostate glands from PEBP4−/− mice.ConclusionThe knockout of PEBP4 in experimental mice led to chronic prostatitis and the reduced expression of PEBP4 in patients with higher risk of chronic and non‐bacterial prostatitis suggested that PEBP4 might act as a protective factor against chronic prostatitis. The knockout of PEBP4 in RWPE‐1 cells led to the increased activation of NF‐κB and IκB, thus indicating that inhibition of PEBP4 faciliated the NF‐κB signaling cascade. Our findings provide a new etiology and therapeutic target for chronic prostatitis.