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. 2024 Jan 4;21:8. doi: 10.1186/s12974-023-02993-6

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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 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. 2 — MIF in AD. Activated glia and especially neurons are the main sources of MIF in AD. Dysregulated glucose metabolism and AGE promote MIF conformational changes leading to disrupted ERK signaling in glia cells. In AD increased CD74 has been found in microglia, neurofibrillary tangles, amyloid β plaques and neurons