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In Situ Blood Vessel Regeneration Using SP (Substance P) and SDF (Stromal Cell-Derived Factor)-1α Peptide Eluting Vascular Grafts.
- Source :
-
Arteriosclerosis, thrombosis, and vascular biology [Arterioscler Thromb Vasc Biol] 2018 Jul; Vol. 38 (7), pp. e117-e134. Date of Electronic Publication: 2018 May 31. - Publication Year :
- 2018
-
Abstract
- Objective: The objective of this study was to develop small-diameter vascular grafts capable of eluting SDF (stromal cell-derived factor)-1α-derived peptide and SP (substance P) for in situ vascular regeneration.<br />Approach and Results: Polycaprolactone (PCL)/collagen grafts containing SP or SDF-1α-derived peptide were fabricated by electrospinning. SP and SDF-1α peptide-loaded grafts recruited significantly higher numbers of mesenchymal stem cells than that of the control group. The in vivo potential of PCL/collagen, SDF-1, and SP grafts was assessed by implanting them in a rat abdominal aorta for up to 4 weeks. All grafts remained patent as observed using color Doppler and stereomicroscope. Host cells infiltrated into the graft wall and the neointima was formed in peptides-eluting grafts. The lumen of the SP grafts was covered by the endothelial cells with cobblestone-like morphology, which were elongated in the direction of the blood flow, as discerned using scanning electron microscopy. Moreover, SDF-1α and SP grafts led to the formation of a confluent endothelium as evaluated using immunofluorescence staining with von Willebrand factor antibody. SP and SDF-1α grafts also promoted smooth muscle cell regeneration, endogenous stem cell recruitment, and blood vessel formation, which was the most prominent in the SP grafts. Evaluation of inflammatory response showed that 3 groups did not significantly differ in terms of the numbers of proinflammatory macrophages, whereas SP grafts showed significantly higher numbers of proremodeling macrophages than that of the control and SDF-1α grafts.<br />Conclusions: SDF-1α and SP grafts can be potential candidates for in situ vascular regeneration and are worthy for future investigations.<br /> (© 2018 American Heart Association, Inc.)
- Subjects :
- Angiogenesis Inducing Agents chemistry
Animals
Aorta, Abdominal diagnostic imaging
Aorta, Abdominal pathology
Aorta, Abdominal physiopathology
Cell Movement drug effects
Cell Proliferation drug effects
Cells, Cultured
Chemokine CXCL12 chemistry
Humans
Male
Mesenchymal Stem Cells drug effects
Neointima
Peptide Fragments chemistry
Prosthesis Design
Rats, Sprague-Dawley
Substance P chemistry
Time Factors
Ultrasonography, Doppler, Color
Vascular Patency
Vascular Remodeling
Angiogenesis Inducing Agents pharmacology
Aorta, Abdominal surgery
Blood Vessel Prosthesis
Blood Vessel Prosthesis Implantation instrumentation
Chemokine CXCL12 pharmacology
Coated Materials, Biocompatible
Collagen Type I chemistry
Neovascularization, Physiologic drug effects
Peptide Fragments pharmacology
Polyesters chemistry
Substance P pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1524-4636
- Volume :
- 38
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Arteriosclerosis, thrombosis, and vascular biology
- Publication Type :
- Academic Journal
- Accession number :
- 29853570
- Full Text :
- https://doi.org/10.1161/ATVBAHA.118.310934