Restoration of angiogenic capacity in senescent endothelial cells by a pharmacological reprogramming approach

Senescent endothelial cells (EC) are key players in the pathophysiology of cardiovascular diseases and are characterized by a reduced angiogenic and regenerative potential. Therefore, targeting these cells has been suggested as an effective therapeutic strategy to reduce vascular disease burden and potentially improve health and lifespan of humans. Here, we aimed to establish a pharmacological, partial reprogramming strategy to improve replicative senescent endothelial cell function in the context of angiogenesis. We demonstrate that our treatment improves tube formation and sprouting capacity but also increases proliferation and migration capacity in vitro. Further, inflammation and DNA damage were reduced in the replicative senescent cells. These processes were initiated by a short and timely-restricted overexpression of the Yamanaka-factors induced by our pharmacological strategy. The advantage of these compounds is that they are FDA approved in their respective concentrations which could pave the way for use in a clinical setting.

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Publication Details

Journal
PLoS ONE
Published
2025-02-28
DOI
https://doi.org/10.1371/journal.pone.0319381
Citations
1
Primary Topic
Telomeres, Telomerase, and Senescence
Type
article
Field-Weighted Citation Impact
1.16
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Restoration of angiogenic capacity in senescent endothelial cells by a pharmacological reprogramming approach

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1 citations
PLoS ONE
Telomeres, Telomerase, and Senescence
1.16
article

Restoration of angiogenic capacity in senescent endothelial cells by a pharmacological reprogramming approach

Susanne Koch, Daniel Sedding, Kai Knöpp, Katrin Kalies, Claudia Pilowski, Leonie Wurmbrand
article en
1 citations

Abstract

Senescent endothelial cells (EC) are key players in the pathophysiology of cardiovascular diseases and are characterized by a reduced angiogenic and regenerative potential. Therefore, targeting these cells has been suggested as an effective therapeutic strategy to reduce vascular disease burden and potentially improve health and lifespan of humans. Here, we aimed to establish a pharmacological, partial reprogramming strategy to improve replicative senescent endothelial cell function in the context of angiogenesis. We demonstrate that our treatment improves tube formation and sprouting capacity but also increases proliferation and migration capacity in vitro. Further, inflammation and DNA damage were reduced in the replicative senescent cells. These processes were initiated by a short and timely-restricted overexpression of the Yamanaka-factors induced by our pharmacological strategy. The advantage of these compounds is that they are FDA approved in their respective concentrations which could pave the way for use in a clinical setting.

PLoS ONEVol. 20(2)
Martin Luther University Halle-Wittenberg (DE)
Openalex Percentile: Top 25%
Telomeres, Telomerase, and Senescence
1.16
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