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. 2023 Apr 18;6:403. doi: 10.1038/s42003-023-04640-5

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© The Author(s) 2023

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a, b Expression of TYRP1, but not TYR or TYRP2, was substantially decreased in Mewo-Z5Z7-DKO cells. Immunoblotting (a) and immunofluorescence staining (b). c, d Expression of TYRP1 in Mewo-Z5Z7-DKO cells was reversed by stable re-expression of ZNT7. Immunoblotting (c) and immunofluorescence staining (d). e Effects of zinc status on the expression of TYRP1. Wild-type (WT) Mewo and Mewo-Z5Z7-DKO cells were cultured in normal medium (N), normal medium supplemented with ZnSO₄ (75 μM), or in zinc-deficient medium (CX) generated using Chelex-treated FCS for 24 h. f TYRP1 mRNA levels were not decreased in Mewo-Z5Z7-DKO cells. In a, c, and e, Tubulin or CNX was detected as a loading control. Each experiment was performed at least three times, and representative results from independent experiments are shown.