CXCR4 regulates macrophage M1 polarization by altering glycolysis to promote prostate fibrosis.

ABSTRACT:

Background

C-X-C receptor 4(CXCR4) is widely considered to be a highly conserved G protein-coupled receptor, widely involved in the pathophysiological processes in the human body, including fibrosis. However, its role in regulating macrophage-related inflammation in the fibrotic process of prostatitis has not been confirmed. Here, we aim to describe the role of CXCR4 in modulating macrophage M1 polarization through glycolysis in the development of prostatitis fibrosis.

Methods

Use inducible experimental chronic prostatitis as a model of prostatic fibrosis. Reduce CXCR4 expression in immortalized bone marrow-derived macrophages using lentivirus. In the fibrotic mouse model, use adenovirus carrying CXCR4 agonists to detect the silencing of CXCR4 and assess the in vivo effects.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC11426013 | biostudies-literature | 2024 Sep

REPOSITORIES: biostudies-literature