Progesterone attenuates thrombin-induced endothelial barrier disruption in the brain endothelial cell line bEnd.3: The role of tight junction proteins and the endothelial protein C receptor

• Published in: Brain research 2015-07, Vol.1613, p.73-80
• Main Authors: Hun Lee, Jeong, Won, Soonmi, Stein, Donald G
• Format: Article
• Language: English
• Subjects: Animals; bEnd.3 endothelial cell; Blood-Brain Barrier - drug effects; Blood-Brain Barrier - metabolism; Blood–brain barrier; Brain Ischemia - metabolism; Cell Line; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Endothelial Protein C Receptor; Mice; Neurology; Permeability; Progesterone; Progesterone - pharmacology; Rats, Sprague-Dawley; Receptors, Cell Surface; Stroke - metabolism; Thrombin; Thrombin - toxicity; Tight junction protein; Tight Junction Proteins - drug effects; Tight Junction Proteins - metabolism
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/j.brainres.2015.04.002

Abstract This study examines the effects of progesterone on blood-brain barrier (BBB) integrity following thrombin administration. Thrombin is expressed in many diseases which affect neural tissue and is associated with breakdown of the BBB. Progesterone has shown protective effects on the BBB in stroke and traumatic brain injury. Methods Mouse brain endothelial (bEnd.3) cells were treated with progesterone (20 μmol/l) for 24 h before thrombin administration (60 U/ml). BBB permeability was measured by transendothelial electrical resistance (TEER), because TEER decrease is associated with BBB compromise. Tight junction (TJ) proteins (occludin, claudin-5, and zonula occludens-1) and endothelial protein C receptor (EPCR) were analyzed. Results Thrombin decreased TEER and progesterone prevented that decrease. TJ proteins and EPCR were also decreased after thrombin treatment and progesterone treatment blocked that effect. Conclusion: Progesterone can attenuate thrombin-induced BBB disruption by blocking the degradation of TJ proteins and EPCR in bEnd.3 cells.