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Induction of Endothelial Differentiation in Cardiac Progenitor Cells Under Low Serum Conditions
Published on: January 7, 2019
Regenerative cell therapy and pharmacotherapeutic intervention in heart failure: Part 1: Cardiovascular progenitor
C Qian1, R G Schoemaker, W H van Gilst
1Department of Experimental Cardiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Insights
Bone marrow-derived endothelial progenitor cells (BM-EPCs) are crucial for blood vessel repair. Understanding their biology and microenvironment is key to developing effective cell therapies for neovascularization and heart failure.
Area of Science:
- Cardiovascular Biology
- Regenerative Medicine
- Cell Therapy
Background:
- Endothelial progenitor cells (EPCs) from bone marrow (BM-EPCs) are implicated in neovascularization and endothelial repair.
- Their role in pharmacological treatments and as therapeutic targets is under investigation.
- The precise biology of EPCs and their niche microenvironments remains poorly understood.
Purpose of the Study:
- To review the involvement of progenitor cells in chronic heart failure.
- To focus on factors that positively influence BM-EPCs.
- To emphasize pharmacological pathways in BM-EPC-mediated neovascularization.
Main Methods:
- Literature review focusing on progenitor cell involvement in heart failure.
- Analysis of factors influencing BM-EPC function.
- Emphasis on pharmacological molecular pathways driving BM-EPC-induced neovascularization.
Main Results:
- Progenitor cells may play a role in chronic heart failure.
- Specific factors can beneficially affect BM-EPCs.
- Pharmacological pathways are crucial for BM-EPC-mediated neovascularization.
Conclusions:
- A deeper understanding of EPC biology and niche signaling is essential for successful angiogenic cell therapy.
- Rational pharmacotherapy targeting BM-EPCs can enhance vascular repair.
- Optimizing BM-EPC function is critical for clinical improvement in vascular repair and angiogenic therapies.
Abstract:
It has been postulated that bone marrow derived endothelial progenitor cells (BM-EPCs) are essential for neovascularisation and endothelial repair and are involved in pharmacological treatment, and even its potential targets. There is no doubt that the ultimate success of angiogenic cell therapy will be determined by an appropriate stimulation of certain angiogenic progenitor cell subpopulations. Unfortunately, the biology of EPCs is still poorly understood. In particular, the understanding of endogenous microenvironments within the progenitor cell niches is critical, and will provide us with information about the signalling systems that supply a basis to develop rational pharmacotherapy to enhance the functional activity of endogenous or transplanted progenitor cells. The final success of clinical improvement of progenitor cell-mediated vascular repair and angiogenic therapy depends on a better understanding of EPC biology and a smart therapeutic design. In the first part of this review we first briefly discuss the possible involvement of progenitor cells in chronic heart failure. In part 2 we focus on factors that beneficially affect BMEPCs, with an emphasis on pharmacological molecular pathways involved in BM-EPC-induced neovascularisation. (Neth Heart J 2008;16:305-9.).
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