Journal Article

DZNE-2026-00206

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Forebrain-specific loss of erythropoietin provokes compensatory upregulation of different EPO receptors.

Butt, U. J. ; Çakır, U. ; Wildenburg, A.-F. ; Curto, Y. ; Ye, L. ; Bansal, V.DZNE* ; Boretius, S. ; Nave, K.-A. ; Singh, M. ; Ehrenreich, H.

2026
Springer Nature [London]

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Please use a persistent id in citations: doi:10.1038/s41380-025-03230-7

Abstract: The procognitive growth factor erythropoietin (EPO) and its canonical receptor, EPOR, have long been recognized to be expressed by most cell types in the brain. Cognitive domains, improved by injections of exogenous EPO or by endogenous, hypoxia-stimulated EPO, include important forebrain functions, namely attention, working memory, drive, and executive performance. To gain mechanistic insight into the involvement of forebrain-expressed EPO, we deleted EPO in mice using as specific cre-driver Emx1. Here, we report that these mutant mice act comparably to their wildtype littermates in a comprehensive behavioral test battery. Importantly, we find that the transcripts of both EPOR and a novel, brain-expressed EPO receptor, EphB4, respond to EPO deletion with compensatory upregulation. EphB4 expression in brain and its increase upon forebrain erasure of EPOR are confirmed by in situ hybridization and immunohistochemistry. The augmented expression of both EPOR and EphB4 and their regulatory intercorrelation may explain why EmxEPO mutants show an even superior performance in the most challenging working memory task. Using the previously published single-nuclei-RNA-seq dataset, we further confirm the suggested compensatory mechanism, wherein EPO loss or reduction drives elevated EPOR expression, adding another layer to the intricate regulation of EPO signaling in hippocampal pyramidal neurons. Collectively, these data may explain the lack of behavioral and negative cognitive consequences upon forebrain-wide EPO elimination.

Keyword(s): Animals (MeSH) ; Erythropoietin: metabolism (MeSH) ; Erythropoietin: genetics (MeSH) ; Prosencephalon: metabolism (MeSH) ; Receptors, Erythropoietin: metabolism (MeSH) ; Receptors, Erythropoietin: genetics (MeSH) ; Mice (MeSH) ; Memory, Short-Term: physiology (MeSH) ; Up-Regulation (MeSH) ; Receptor, EphB4: metabolism (MeSH) ; Receptor, EphB4: genetics (MeSH) ; Male (MeSH) ; Hippocampus: metabolism (MeSH) ; Signal Transduction (MeSH) ; Brain: metabolism (MeSH) ; Mice, Inbred C57BL (MeSH) ; Mice, Transgenic (MeSH) ; Mice, Knockout (MeSH) ; Cognition: physiology (MeSH) ; Erythropoietin ; Receptors, Erythropoietin ; Receptor, EphB4 ; Epo protein, mouse

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Contributing Institute(s):

1. Biomedical Data Science (AG Bansal)

Research Program(s):

1. 354 - Disease Prevention and Healthy Aging (POF4-354) (POF4-354)

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Database coverage:
; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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