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. 2017 Jan 28;8:19. doi: 10.1186/s13287-017-0475-8

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© The Author(s). 2017

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. 10 — Densitometric analysis and immunoblotting of premature senescence markers that behaved differently in IRI + huMSC rats than in IRI + aMSC rats. Immunoblots and densitometric analysis of samples from IRI + huMSC (n = 7) and IRI + aMSC rats (n = 4), on D2. a Klotho. b MnSOD. ^a p < 0.05 vs IRI + huMSC. aMSC adipose-derived mesenchymal stromal cell, huMSC human umbilical cord-derived mesenchymal stromal cell, IRI ischaemia/reperfusion injury, MnSOD manganese superoxide dismutase