TY - JOUR
T1 - Expression and Cellular Localization of 15-Hydroxy-Prostaglandin-Dehydrogenase in Abdominal Aortic Aneurysm
AU - Solà-Villà, David
AU - Dilme, Jaime
AU - Rodríguez, Cristina
AU - Soto Carricas, Begoña
AU - Vila, Luis
AU - Escudero, José-Román
AU - Martínez-González, José
AU - Camacho, Mercedes
PY - 2015
Y1 - 2015
N2 - PGE has been implicated in abdominal aortic aneurysm (AAA) associated hypervascularization. PGE-metabolism involves 15-hydroxyprostaglandin-dehydrogenase (15-PGDH) the expression of which in AAA is unknown. The aim of this study was to examine the expression and cell distribution of 15-PGDH in AAA. Here, we show that 15-PGDH mRNA levels were significantly higher in aorta samples from patients undergoing AAA repair than in those from healthy multiorgan donors. Consequently, the ratio of metabolized PGE secreted by aortic samples was significantly higher in AAA. AAA production of total PGE and PGE metabolites correlated positively with PGI production, while the percentage of metabolized PGE correlated negatively with the total amount of PGE and with PGI. Transcript levels of 15-PGDH were statistically associated with leukocyte markers but did not correlate with microvascular endothelial cell markers. Immunohistochemistry revealed 15-PGDH in the areas of leukocyte infiltration in AAA samples, mainly associated with CD45-positive cells, but not in normal aorta samples. We provide new data concerning 15-PGDH expression in human AAA, showing that 15-PGDH is upregulated in AAA and mainly expressed in infiltrating leukocytes. Our data suggest that microvasculature was not involved in PGE catabolism, reinforcing the potential role of microvasculature derived PGE in AAA-associated hypervascularization.
AB - PGE has been implicated in abdominal aortic aneurysm (AAA) associated hypervascularization. PGE-metabolism involves 15-hydroxyprostaglandin-dehydrogenase (15-PGDH) the expression of which in AAA is unknown. The aim of this study was to examine the expression and cell distribution of 15-PGDH in AAA. Here, we show that 15-PGDH mRNA levels were significantly higher in aorta samples from patients undergoing AAA repair than in those from healthy multiorgan donors. Consequently, the ratio of metabolized PGE secreted by aortic samples was significantly higher in AAA. AAA production of total PGE and PGE metabolites correlated positively with PGI production, while the percentage of metabolized PGE correlated negatively with the total amount of PGE and with PGI. Transcript levels of 15-PGDH were statistically associated with leukocyte markers but did not correlate with microvascular endothelial cell markers. Immunohistochemistry revealed 15-PGDH in the areas of leukocyte infiltration in AAA samples, mainly associated with CD45-positive cells, but not in normal aorta samples. We provide new data concerning 15-PGDH expression in human AAA, showing that 15-PGDH is upregulated in AAA and mainly expressed in infiltrating leukocytes. Our data suggest that microvasculature was not involved in PGE catabolism, reinforcing the potential role of microvasculature derived PGE in AAA-associated hypervascularization.
U2 - 10.1371/journal.pone.0136201
DO - 10.1371/journal.pone.0136201
M3 - Article
C2 - 26287481
SN - 1932-6203
VL - 10
JO - PLoS ONE
JF - PLoS ONE
ER -