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. 2021 Sep 10;12:501. doi: 10.1186/s13287-021-02570-9

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© The Author(s) 2021

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. 7 — A model of the anti-hyperpigmentation of hAMSC-CM. Upon UV radiation, keratinocytes secrete α-MSH to induce MITF expression and promote melanogenesis in melanocyte. hAMSC-CM and hAMSCs-derived exosomes reduce excessive melanin deposition by suppressing melanogenesis and promoting melanosome degradation. Furthermore, exosomes-derived miR-181a-5p and miR-199a reduce MITF expression to suppress melanin content and regulating autophagy flux to promote melanosome degradation, respectively