Authors
Hyo-Jin Kim, Jeong-Hyung Lee, Cheol Hwangbo
Published in
Aging cell. Volume 25. Issue 10. Pages e70757.
Abstract
Traditionally viewed as a classic sentinel of innate immunity, Toll-like receptor 4 (TLR4) has emerged as a crucial pathological driver within the vascular endothelium, with its identity dictated by cell-type specificity, microenvironmental context, and fluctuating expression levels. This review critically examines the dual functional nature of endothelial TLR4, delineating how it transitions into a primary driver of vascular aging and organ-specific vascular pathologies. The profound spatial, temporal, and cellular heterogeneities of TLR4 signaling expose the fundamental inadequacies of conventional systemic pan-TLR4 blockade, which has repeatedly failed in clinical trials due to severe immunosuppression and metabolic disruptions. To bypass these limitations, we propose a precision senotherapeutic framework utilizing advanced drug delivery systems-such as Vascular cell adhesion molecule-1 (VCAM-1) or E-selectin-targeted nanoparticles and genetically engineered plant-derived exosomes-to compartmentalize TLR4 inhibition within pathologically altered endothelial sub-populations. By shifting the clinical paradigm from indiscriminate receptor suppression to spatiotemporal fine-tuning, this conceptual framework provides a rational blueprint for next-generation anti-aging therapies aimed at restoring vascular homeostasis throughout the aging process.
PMID:
42834845
Bibliographic data and abstract were imported from PubMed on 06 Oct 2026.
Read full publication at:
Please sign in
to see all details.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 11
- Comments 0