TY - JOUR
T1 - Specific induction of adhesion molecules in human vascular endothelial cells by rat experimental pancreatitis-associated ascitic fluids
AU - Masamune, Atsushi
AU - Shimosegawa, Tooru
AU - Kimura, Kenji
AU - Fujita, Motokazu
AU - Sato, Akihiko
AU - Koizumi, Masaru
AU - Toyota, Takayoshi
PY - 1999/3
Y1 - 1999/3
N2 - The molecular mechanisms that link acute pancreatitis (AP) and multiple organ failure remain unknown. To clarify the role of endothelial activation, we examined the effects of ascitic fluids from rats with experimental pancreatitis on the expression of adhesion molecules in human umbilical vein endothelial cells (HUVECs). Necrotizing hemorrhagic pancreatitis was induced with sodium taurocholate. Six and 24 h later, peritoneal exudates were collected, centrifuged and HUVECs were treated with the supernatants. The expression of E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) was quantified by enzyme-linked immunosorbent assay. Induction of mRNA was assessed by reverse-transcriptase polymerase chain reaction. The activation of transcription factors was examined by electrophoretic mobility shift assay. The expression of ICAM-1 in the tissues was examined immunohistochemically. ICAM-1 and VCAM-1, but not E- selectin expression was upregulated with comparable mRNA induction. Nuclear factor κB was activated, while activator protein-1 binding activity was not altered. Immunohistochemically, enhanced ICAM-1 expression was observed in the pancreas and lung, but not in the liver. Ascitic fluids may contain soluble factors responsible for the transcriptional activation of endothelial adhesion molecules, and ICAM-1 may play roles in the pathogenesis of complicated AP.
AB - The molecular mechanisms that link acute pancreatitis (AP) and multiple organ failure remain unknown. To clarify the role of endothelial activation, we examined the effects of ascitic fluids from rats with experimental pancreatitis on the expression of adhesion molecules in human umbilical vein endothelial cells (HUVECs). Necrotizing hemorrhagic pancreatitis was induced with sodium taurocholate. Six and 24 h later, peritoneal exudates were collected, centrifuged and HUVECs were treated with the supernatants. The expression of E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) was quantified by enzyme-linked immunosorbent assay. Induction of mRNA was assessed by reverse-transcriptase polymerase chain reaction. The activation of transcription factors was examined by electrophoretic mobility shift assay. The expression of ICAM-1 in the tissues was examined immunohistochemically. ICAM-1 and VCAM-1, but not E- selectin expression was upregulated with comparable mRNA induction. Nuclear factor κB was activated, while activator protein-1 binding activity was not altered. Immunohistochemically, enhanced ICAM-1 expression was observed in the pancreas and lung, but not in the liver. Ascitic fluids may contain soluble factors responsible for the transcriptional activation of endothelial adhesion molecules, and ICAM-1 may play roles in the pathogenesis of complicated AP.
KW - Acute pancreatitis
KW - Endothelial cell
KW - Experimental pancreatitis
KW - Intercellular adhesion molecule-1
KW - Nuclear factor-κB
UR - http://www.scopus.com/inward/record.url?scp=0032928757&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032928757&partnerID=8YFLogxK
U2 - 10.1097/00006676-199903000-00005
DO - 10.1097/00006676-199903000-00005
M3 - Article
C2 - 10090411
AN - SCOPUS:0032928757
SN - 0885-3177
VL - 18
SP - 141
EP - 150
JO - Pancreas
JF - Pancreas
IS - 2
ER -