Glomerular Outgrowth as an Ex Vivo Assay to Analyze Pathways Involved in Parietal Epithelial Cell Activation

Author(s):  
Jennifer Eymael ◽  
Laura Miesen ◽  
Fieke Mooren ◽  
Jitske Jansen ◽  
Jack Wetzels ◽  
...  
2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Hua Su ◽  
Shan Chen ◽  
Fang-Fang He ◽  
Yu-Mei Wang ◽  
Philip Bondzie ◽  
...  

The glomerular parietal epithelial cells (PECs) have aroused an increasing attention recently. The proliferation of PECs is the main feature of crescentic glomerulonephritis; besides that, in the past decade, PEC activation has been identified in several types of noninflammatory glomerulonephropathies, such as focal segmental glomerulosclerosis, diabetic glomerulopathy, and membranous nephropathy. The pathogenesis of PEC activation is poorly understood; however, a few studies delicately elucidate the potential mechanisms and signaling pathways implicated in these processes. In this review we will focus on the latest observations and concepts about PEC activation in glomerular diseases and the newest identified signaling pathways in PEC activation.


2013 ◽  
Vol 83 (6) ◽  
pp. 988-990 ◽  
Author(s):  
Mariya T. Sweetwyne ◽  
Katalin Susztak

2013 ◽  
Vol 183 (6) ◽  
pp. 1769-1778 ◽  
Author(s):  
Paola Rizzo ◽  
Norberto Perico ◽  
Elena Gagliardini ◽  
Rubina Novelli ◽  
Malcolm R. Alison ◽  
...  

2012 ◽  
Vol 7 (11) ◽  
pp. 1852-1858 ◽  
Author(s):  
Huma Fatima ◽  
Marcus J. Moeller ◽  
Bart Smeets ◽  
Hai-Chun Yang ◽  
Vivette D. D’Agati ◽  
...  

2017 ◽  
Vol 28 (12) ◽  
pp. 3563-3578 ◽  
Author(s):  
Yosu Luque ◽  
Olivia Lenoir ◽  
Philippe Bonnin ◽  
Lise Hardy ◽  
Anna Chipont ◽  
...  

2014 ◽  
Vol 95 (3) ◽  
pp. 273-282 ◽  
Author(s):  
Alexander Holderied ◽  
Simone Romoli ◽  
Jonathan Eberhard ◽  
Lukas A Konrad ◽  
Satish K Devarapu ◽  
...  

1977 ◽  
Vol 37 (01) ◽  
pp. 154-161 ◽  
Author(s):  
B. A Janik ◽  
S. E Papaioannou

SummaryUrokinase, streptokinase, Brinase, trypsin, and SN 687, a bacterial exoprotease, have been evaluated in an ex vivo assay system. These enzymes were injected into rabbits and the fibrinolytic activity as well as other coagulation parameters were measured by in vitro techniques. Dose-response correlations have been made using the euglobulin lysis time as a measure of fibrinolytic activity and the 50% effective dose has been determined for each enzyme. Loading doses, equal to four times the 50% effective dose, were administered to monitor potential toxicity revealing that Brinase, trypsin, and SN 687 were very toxic at this concentration.Having established the 50% effective dose for each enzyme, further testing was conducted where relevant fibrinolytic and coagulation parameters were measured for up to two days following a 50% effective dose bolus injection of each enzyme. Our results have demonstrated that urokinase and streptokinase are plasminogen activators specifically activating the rabbit fibrinolytic system while Brinase, trypsin and SN 687 increase the general proteolytic activity in vivo.The advantages of this ex vivo assay system for evaluating relative fibrinolytic potencies and side effects for plasminogen activators and fibrinolytic proteases have been discussed.


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