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. 2016 Feb 4;23:24. doi: 10.1186/s12929-016-0242-7

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© Chen et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 7 — Neither elastase nor cathepsin G mediated cleavage of the soluble urokinase-type plasminogen activator (uPA) receptor (suPAR) in a focal segmental glomerulosclerosis (FSGS) mouse model. Plasma activities of elastase (a) and cathepsin G (b) were determined in the wild-type (WT) and uPA^−/− groups during the course of the experiment until 4 weeks after Adriamycin treatment. ^# p < 0.05 vs. week 0 (W0); *p < 0.05 vs. the WT