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. 2020 Sep 18;21:402. doi: 10.1186/s12882-020-02060-9

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 3 — DPP-4 activity in human cultured podocytes with or without ADR treatment. a DPP-4 activity in injured podocytes was significantly higher than that in controls. b, c DPP-4 activity in podocytes using saxagliptin (100 nM) was significantly lower than that in podocytes using 1 nM saxagliptin at days 2 and 4. DPP-4 activity was not significantly reduced in control podocytes by treatment with saxagliptin. **: P < 0.01, ***: P < 0.001, ****: P < 0.0001