Citations 3

Vascular protection by young circulating extracellular vesicles ameliorates aging-related pulmonary fibrosis

American Journal of Physiology-Cell Physiology | May 24, 2025 | Volume: 329 | Issue: 1 | Pages: C159-C169

10.1152/ajpcell.00022.2025 | PMID 40411768

This study demonstrates that circulating extracellular vesicles (cEVs) isolated from young mice reverse the transcriptional alterations of the aged mouse pulmonary vasculature, leading to a more youthful endothelial transcriptional phenotype. As a result of this vascular phenotype, aged mice are protected from bleomycin-induced pulmonary fibrosis. These findings highlight the therapeutic potential of targeting vascular aging to alleviate pulmonary fibrosis.
Circulating Extracellular Vesicles Isolated From Young Mice Protect Endothelial Cells and Exert Anti-fibrotic Effects In Vivo and Ex Vivo

B65. IMMUNE AND ENDOTHELIAL CELLS HIT BACK AT LUNG REPAIR | May 1, 2023 | Volume: No volume available | Issue: No issue available | Pages: A3959-A3959

10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a3959

Pim-1 kinase is a positive feedback regulator of the senescent lung fibroblast inflammatory secretome

American Journal of Physiology-Lung Cellular and Molecular Physiology | October 12, 2022 | Volume: 323 | Issue: 6 | Pages: L685-L697

10.1152/ajplung.00023.2022 | PMID 36223640

Cellular senescence is emerging as a driver of idiopathic pulmonary fibrosis (IPF), a progressive and fatal disease with limited effective therapies. The senescence-associated secretory phenotype (SASP), involving the release of inflammatory cytokines and profibrotic growth factors by senescent cells, is thought to be a product of multiple cell types in IPF, including lung fibroblasts. NF-κB is a master regulator of the SASP, and its activity depends on the phosphorylation of p65/RelA. The purpose of this study was to assess the role of Pim-1 kinase as a driver of NF-κB-induced production of inflammatory cytokines from low-passage IPF fibroblast cultures displaying markers of senescence. Our results demonstrate that Pim-1 kinase phosphorylates p65/RelA, activating NF-κB activity and enhancing IL-6 production, which in turn amplifies the expression of PIM1, generating a positive feedback loop. In addition, targeting Pim-1 kinase with a small molecule inhibitor dramatically inhibited the expression of a broad array of cytokines and chemokines in IPF-derived fibroblasts. Furthermore, we provide evidence that Pim-1 overexpression in low-passage human lung fibroblasts is sufficient to drive premature senescence, in vitro. These findings highlight the therapeutic potential of targeting Pim-1 kinase to reprogram the secretome of senescent fibroblasts and halt IPF progression.