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Bone marrow cell-mediated cardiovascular repair: potential of combined therapies
Claudio Napoli1, Ciro Maione, Concetta Schiano
1Department of General Pathology, Division of Clinical Pathology and Excellence Research Center on Cardiovascular Diseases, 1st School of Medicine, II University of Naples, Italy. claunap@tin.it
Insights
Bone-marrow cell (BMC) transplantation shows promise for cardiovascular healing. Combined therapies with antioxidants, L-arginine, and gene therapy may enhance BMC efficacy for restoring vascularization and organ function.
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Cell Therapy
Background:
- Bone-marrow cells (BMCs) show potential in cardiovascular repair via specific molecular pathways.
- Ischemia generates harmful oxygen radicals, suggesting antioxidant and L-arginine (nitric oxide precursor) treatments could be beneficial.
- Previous studies indicate enhanced neovascularization with BMCs when co-treated with vitamins E and C, and L-arginine.
Purpose of the Study:
- To discuss the clinical potential of BMC transplantation alone and in combined therapies for cardiovascular diseases.
- To explore mechanisms of BMC mobilization, differentiation, and incorporation.
- To evaluate strategies for restoring organ vascularization and function using BMCs.
Main Methods:
- Review of recent evidence on BMCs and cardiovascular healing.
- Analysis of molecular pathways involved (CXCR4/SDF-1, thymosin beta(4), integrin alpha(4)beta(1)).
- Discussion of combined therapeutic approaches including antioxidants, L-arginine, and gene therapy.
Main Results:
- BMCs contribute to cardiovascular healing through specific molecular pathways.
- Antioxidants and L-arginine may augment BMC therapy benefits.
- Combined BMC therapy with vitamins and L-arginine shows enhanced neovascularization capacity.
- Clinical trials with BMCs for cardiovascular diseases have yielded mixed to positive results, with ongoing studies.
Conclusions:
- BMC transplantation holds clinical potential for cardiovascular disease treatment.
- Combined therapies, including antioxidants and L-arginine, may improve outcomes.
- Further research into BMC mechanisms and combined strategies is warranted to restore vascularization and organ function.
Abstract:
Recent evidence indicates that bone-marrow cells (BMCs) can contribute to the healing process of the injured cardiovascular system via the chemokine receptor CXCR4/SDF-1, thymosin beta(4) and integrin alpha(4)beta(1) molecular pathways. During tissue ischemia overwhelming numbers of detrimental oxygen radicals are generated, and therefore treatment with antioxidants and L-arginine, the precursor of nitric oxide (NO), could induce beneficial effects beyond those achieved by BMC transplantation alone. Recent studies have reported that BMCs have enhanced neovascularization capacity in cotreatment with alpha-tocopherol (vitamin E), ascorbic acid (vitamin C) and L-arginine. Moreover, BMC therapy can be combined with gene therapy. Clinical trials employing BMCs in the treatment of cardiovascular diseases have been completed with mixed or positive results, and several trials are ongoing. Here, we discuss the clinical potential of BMC transplantation alone and in combined therapy that aims to restore organ vascularization and function. We also consider the mechanisms of mobilization, differentiation and incorporation of BMCs.
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