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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. 4 — Cytoskeleton-associated proteins were protected by saxagliptin after podocyte injuries by ADR. a In the control and ADR + saxagliptin group, synaptopodin and stress fibers were observed in the cytoplasm. In the ADR group, synaptopodin and stress fibers were not observed in the cytoplasm. b Area of synaptopodin/cell and stress fibers/cell in the saxagliptin group was maintained compared to that in the ADR group. c Levels of synaptopodin and RhoA in the ADR group was significantly lower than that in the control and ADR + saxagliptin group. *: P < 0.05, ***: P < 0.001