| Literature DB >> 34939225 |
Lulu Liu1,2, Jinjin Zhong1, Bilin Chen1, Weiping Wang3, Haiyan Xi3, Xin Su1,3.
Abstract
Given the increasing incidence of pulmonary aspergillosis, it is important to understand the natural defense mechanisms by which the body can kill Aspergillus fumigatus conidia. Pentraxin 3 (PTX3) plays a nonredundant role in resistance to A. fumigatus. Here, we found that the key predicted PTX3 transcription factor, CCAAT/enhancer-binding protein δ (CEBPD), was up-regulated during A. fumigatus conidia infection. Functionally, CEBPD significantly promoted the expression of PTX3 and the phagocytic ability of macrophages. Mechanistically, CEBPD activated the PTX3 by directly binding to the promoter region of the PTX3 gene. We also showed that the RNA-binding protein human antigen R promoted CEBPD expression. These findings provide new insights into the crucial role of CEBPD in the phagocytosis of A. fumigatus conidia by macrophages and highlight this protein as a potential therapeutic target for invasive pulmonary aspergillosis. ©2021 Society for Leukocyte Biology.Entities:
Keywords: A. fumigatus; CEBPD; HuR; PTX3; pulmonary aspergillosis
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Year: 2021 PMID: 34939225 DOI: 10.1002/JLB.4MA1121-451RR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 6.011