TMPRSS11E-mediated TFR1 cleavage influences IFN-gammaR2 internalization and the macrophage innate response #MMPMID41339525
Wang T; Chen Z; Jiang Y; Wang N; Zhang W; Wang X; Ding J; Liu L; Hua Z; Fang L; Li S
Commun Biol 2025[Dec]; 8 (1): 1741 PMID41339525show ga
TMPRSS11E is a serine protease whose expression is upregulated in macrophages during inflammation. Here, we identify TFR1 as an interacting protein of TMPRSS11E via LC-MS/MS. In vitro experiments reveal that TMPRSS11E cleaves TFR1 and releases soluble TFR1 (sTFR1). In alveolar macrophages isolated from pneumonia patients and inflammatory animal models or cultured LPS-challenged cell lines, upregulated TMPRSS11E expression and significantly increased sTFR1 release are observed. Moreover, THP-1 cells stably expressing TMPRSS11E present decreased iron uptake, increased cell surface IFN-gammaR2 accumulation, and a stronger response to IFN-gamma stimulation. During M0 macrophage differentiation to the pro-inflammatory M1 phenotype, the specific induction of TMPRSS11E, decreased cell surface TFR1, and increased IFN-gammaR2 cell membrane localization are also observed. Taken together, our results suggest that TMPRSS11E contributes to M1 macrophage differentiation by regulating iron uptake and affecting IFN-gammaR2 internalization through TFR1 cleavage, indicating that TMPRSS11E plays an important role in iron homeostasis and the innate immune response.
Commun+Biol 2025 ; 8 (1): 1741
