Endothelial toll‐like receptor 4 maintains lung integrity via epigenetic suppression of p16INK4a. Issue 3 (20th February 2019)

• Record Type: Journal Article
• Authors: Kim, So‐Jin; Shan, Peiying; Hwangbo, Cheol; Zhang, Yi; Min, Jin‐Na; Zhang, Xuchen; Ardito, Taylor; Li, Alfred; Peng, Tien; Sauler, Maor; Lee, Patty J.
• Is Part Of: Aging cell. Volume 18:Issue 3(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-02-20
• Subjects: aging -- cellular senescence -- emphysema -- HDAC2 -- p16INK4a -- toll‐like receptor 4; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.12914
• Languages: English
• ISSNs: 1474-9718

Abstract

Abstract: We previously reported that the canonical innate immune receptor toll‐like receptor 4 (TLR4) is critical in maintaining lung integrity. However, the molecular mechanisms via which TLR4 mediates its effect remained unclear. In the present study, we identified distinct contributions of lung endothelial cells (Ec) and epithelial cells TLR4 to pulmonary homeostasis using genetic‐specific, lung‐ and cell‐targeted in vivo methods. Emphysema was significantly prevented via the reconstituting of human TLR4 expression in the lung Ec of TLR4−/− mice. Lung Ec‐silencing of TLR4 in wild‐type mice induced emphysema, highlighting the specific and distinct role of Ec‐expressed TLR4 in maintaining lung integrity. We also identified a previously unrecognized role of TLR4 in preventing expression of p16 INK4a, a senescence‐associated gene. Lung Ec‐p16 INK4a ‐silencing prevented TLR4−/− induced emphysema, revealing a new functional role for p16 INK4a in lungs. TLR4 suppressed endogenous p16 INK4a expression via HDAC2‐mediated deacetylation of histone H4. These findings suggest a novel role for TLR4 in maintaining of lung homeostasis via epigenetic regulation of senescence‐related gene expression.