Thrombospondins Differentially Regulate Proteins Involved in Arterial Remodeling
Language English Country Czech Republic Media print-electronic
Document type Journal Article
Grant support
R01 HL133577
NHLBI NIH HHS - United States
PubMed
31647293
DOI
10.33549/physiolres.934148
PII: 934148
Knihovny.cz E-resources
- MeSH
- Arteries metabolism MeSH
- Cartilage Oligomeric Matrix Protein biosynthesis MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Myocytes, Smooth Muscle metabolism MeSH
- Vascular Remodeling physiology MeSH
- Muscle, Smooth, Vascular metabolism MeSH
- Thrombospondin 1 biosynthesis MeSH
- Thrombospondins biosynthesis MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cartilage Oligomeric Matrix Protein MeSH
- Thrombospondin 1 MeSH
- thrombospondin 2 MeSH Browser
- Thrombospondins MeSH
- TSP5 protein, human MeSH Browser
Thrombospondins (TSPs) are matricellular glycoproteins expressed in response to vascular injury. TSP-1 and TSP-2 are promotors of arterial remodeling while TSP-5 is believed to be protective. The current study assessed the differential effect of TSPs on protein expression in vascular smooth muscle cells (VSMCs). We hypothesized that TSP-1, TSP-2 and TSP-5 would regulate VSMC proteins involved in arterial remodeling. Human VSMCs were exposed to TSP-1, -2, -5 or serum free media (24 hours). Cell lysates were used to assess the targets TSP-1, TSP-2, TSP-5 and CD44), while the culture media was used to detect TGF-ß1, PDGF-BB, ANGPTL-4 and IL-8. Statistical analysis was performed by t-test and p< 0.05 was considered significant. All TSPs increased their own expression and TSP-5 increased TSP-2. TSP-1 and TSP-2 increased production of ANGPTL-4 and PDGF-BB, while TSP-5 only increased ANGPTL-4. TSP-1 increased exclusively TGF-ß1 and CD44 production. TSP-2 increased TSP-1 expression. All TSPs decreased IL-8. The findings suggest that TSP-1 and TSP-2 may promote vascular remodeling, in part, by increasing ANGPTL-4, PDGF-BB and their own expression. TSP-5 did not upregulate the inflammatory mediators TSP-1, PDGF-BB or TGF-ß1, but upregulated its own expression, which could be a protective mechanism against the response to vascular injury.
References provided by Crossref.org