Current perspective of pathophysiological and interventional effects on endothelial progenitor cell biology: focus on
Bert R Everaert1, Emeline M Van Craenenbroeck, Vicky Y Hoymans
1Laboratory of Cell Biology and Histology, University of Antwerp, Antwerp, Belgium.
Insights
Cardiovascular risk factors impair endothelial progenitor cells (EPCs), crucial for blood vessel repair. Interventions targeting the PI3K/Akt/eNOS pathway may restore EPC function and aid cardiovascular disease recovery.
Area of Science:
- Cardiovascular Biology
- Regenerative Medicine
- Cellular Biology
Background:
- Endothelial progenitor cells (EPCs) are vital for maintaining cardiovascular health.
- EPCs originate in bone marrow and migrate to sites of vascular injury.
- Their function can be compromised by cardiovascular risk factors.
Purpose of the Study:
- To review the impact of cardiovascular risk factors on EPC biology.
- To explore interventions that restore EPC function.
- To highlight the role of the PI3K/Akt/eNOS pathway in EPCs.
Main Methods:
- Literature review focusing on EPCs and cardiovascular disease.
- Analysis of the PI3K/Akt/eNOS pathway's role in EPCs.
- Examination of pharmacological, dietary, and lifestyle interventions.
Main Results:
- Cardiovascular risk factors negatively affect EPC mobilization, differentiation, and homing.
- The PI3K/Akt/eNOS pathway is central to EPC function.
- Various interventions show potential to improve EPC biology.
Conclusions:
- Restoring EPC function is a promising strategy for cardiovascular disease treatment.
- Targeting the PI3K/Akt/eNOS pathway offers therapeutic potential.
- Lifestyle and pharmacological interventions can enhance EPC regenerative capacity.
Abstract:
For more than a decade, endothelial progenitor cells (EPCs) have been implicated in cardiovascular homeostasis. EPCs are believed to reside within the bone marrow in close contact with surrounding stromal cells, and, under stimulation of pro-inflammatory cytokines, EPCs are mobilized out of the bone marrow. Hereafter circulating EPCs home to peripheral tissues, undergoing further proliferation and differentiation. Under certain pathophysiologic conditions this process seems to be blunted, resulting in a reduced capacity of EPCs to engage in vasculogenesis at sites of endothelial injury or tissue ischemia. In this review, we focus on the effects of traditional cardiovascular risk factors on EPC biology and we explore whether pharmacological, dietary and lifestyle interventions can favorably restore EPC mobilization, differentiation, homing and angiogenic properties. Because the PI3K/Akt/eNOS pathway plays a pivotal role in the process of EPC mobilization, migration and homing, we specifically emphasize the involvement of PI3K, Akt and eNOS in EPC biology under these different (patho)physiologic conditions. (Pre)clinically used drugs or lifestyle interventions that have been shown to ameliorate EPC biology are reviewed. These treatment strategies remain attractive targets to restore the regenerative capacity of EPCs in cardiovascular diseases.
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