Lipocalin-2-expressing red pulp macrophages link ischemic stroke to systemic immune reprogramming in mice and humans
- 1Goethe University Frankfurt, Institute of General Pharmacology and Toxicology, Pharmazentrum Frankfurt, 60590 Frankfurt am Main, Germany
Abstract
Background Acute ischemic stroke (AIS) triggers profound systemic immune alterations that contribute to post-stroke infections. The spleen is a key peripheral immune organ affected by AIS, but the molecular mediators linking cerebral ischemia to splenic immune dysfunction remain incompletely understood. Lipocalin-2 (LCN2) is an acute-phase protein implicated in neuroinflammation and host defense, yet its peripheral regulation, cellular sources and immune-modulatory actions after AIS remain unclear. Methods Male, 10-12-week-old C57BL/6J mice underwent transient middle cerebral artery occlusion (tMCAO) or sham surgery. Spleens were collected 24 hours, 3 days, or 7 days post-stroke for 3-MACE-Seq transcriptomics, multiplex cytokine profiling, RT-qPCR, immunoblotting, and immunofluorescence. Murine T cells and monocytes were magnetically isolated, stimulated with recombinant LCN2 protein or vehicle, and analyzed using (i) RT-qPCR of LPS-induced proinflammatory cytokines (Il1b, Il6, Tnf), (ii) LCN2-driven T cell chemotaxis, (iii) FACS-based phenotyping, (iv) FACS-based phagocytosis of pHrodo-labeled E. coli bioparticles, and (v) FACS-based quantification of reactive oxygen species (ROS) using DHR-123. Human plasma samples and post-mortem spleens from three patients with ischemic stroke and one non-stroke control were analyzed for LCN2 expression and cellular localization. Untouched human monocytes from healthy donors were exposed to recombinant LCN2 and assessed by flow cytometry for antigen-presentation, co-stimulatory markers, phagocytosis and ROS production. Results Transcriptomics revealed robust, biphasic splenic Lcn2 upregulation at 24 hours and 7 days after tMCAO. LCN2 localized predominantly to F4/80+ red pulp macrophages (RPMs), and accumulated at RPM-associated CD3+ contact sites. AIS induced a broad suppression of splenic innate and adaptive cytokine networks. Recombinant LCN2 induced T cell hyporesponsiveness, suppressed Il6 and Tnf induction, and impaired CCL5-directed chemotaxis. In monocytes, LCN2 promoted a shift toward Ly6Clow phenotypes, enhanced phagocytosis of E. coli, and uncoupled phagocytosis from ROS production. In human ischemic stroke spleens, LCN2 was detected in CD68+ RPMs and at RPM-associated immune-cell contact sites, consistent with the murine splenic phenotype. In line with the murine findings, human monocytes exposed to LCN2 displayed increased E. coli uptake but reduced ROS, alongside reduced HLA-DR, CD80, CD206, and CD11b expression. Conclusions AIS induces a conserved splenic LCN2-expressing RPM niche in mice and humans. Recombinant LCN2 is sufficient to reprogram T cells and monocytes toward hyporesponsive, tolerogenic and phagocytosis-ROS-uncoupled states, thereby linking cerebral ischemia to systemic immune dysfunction. These findings identify LCN2-expressing RPMs as a translationally relevant immunoregulatory niche after AIS and nominate receptor-specific LCN2 signaling as a candidate pathway for future studies aimed at mitigating post-stroke immunodepression and infection susceptibility without compromising antimicrobial host defense.
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BibTeX
@misc{lucaciu2026lipocalin2expressing,
title = {{Lipocalin-2-expressing red pulp macrophages link ischemic stroke to systemic immune reprogramming in mice and humans}},
author = {A. Lucaciu and P. Wurzel and S. R. Rasmussen and E. Lueckhoff and F. Mayser and J. Benjamin and R.-I. Kestner and V. Haas and L. S. Huber and D. Bevara and N. Landvogt and M. Glueck and K. Gertz and R. Raspe and S. Subramanian and C. Welsch and J. Bein and P. J. Wild and H. Radbruch and C. Grefkes and A. Strzelczyk and W. Pfeilschifter and M. Sieweke and J. Pfeilschifter and J. Subburayalu and R. Vutukuri},
howpublished = {bioRxiv},
year = {2026},
month = jun,
doi = {10.64898/2026.06.23.733904},
url = {https://www.biorxiv.org/content/10.64898/2026.06.23.733904v2},
note = {CC BY},
}
RIS
TY - UNPB
TI - Lipocalin-2-expressing red pulp macrophages link ischemic stroke to systemic immune reprogramming in mice and humans
AU - A. Lucaciu
AU - P. Wurzel
AU - S. R. Rasmussen
AU - E. Lueckhoff
AU - F. Mayser
AU - J. Benjamin
AU - R.-I. Kestner
AU - V. Haas
AU - L. S. Huber
AU - D. Bevara
AU - N. Landvogt
AU - M. Glueck
AU - K. Gertz
AU - R. Raspe
AU - S. Subramanian
AU - C. Welsch
AU - J. Bein
AU - P. J. Wild
AU - H. Radbruch
AU - C. Grefkes
AU - A. Strzelczyk
AU - W. Pfeilschifter
AU - M. Sieweke
AU - J. Pfeilschifter
AU - J. Subburayalu
AU - R. Vutukuri
PY - 2026
DA - 2026/06/23
PB - bioRxiv
DO - 10.64898/2026.06.23.733904
UR - https://www.biorxiv.org/content/10.64898/2026.06.23.733904v2
AB - Background Acute ischemic stroke (AIS) triggers profound systemic immune alterations that contribute to post-stroke infections. The spleen is a key peripheral immune organ affected by AIS, but the molecular mediators linking cerebral ischemia to splenic immune dysfunction remain incompletely understood. Lipocalin-2 (LCN2) is an acute-phase protein implicated in neuroinflammation and host defense, yet its peripheral regulation, cellular sources and immune-modulatory actions after AIS remain unclear. Methods Male, 10-12-week-old C57BL/6J mice underwent transient middle cerebral artery occlusion (tMCAO) or sham surgery. Spleens were collected 24 hours, 3 days, or 7 days post-stroke for 3-MACE-Seq transcriptomics, multiplex cytokine profiling, RT-qPCR, immunoblotting, and immunofluorescence. Murine T cells and monocytes were magnetically isolated, stimulated with recombinant LCN2 protein or vehicle, and analyzed using (i) RT-qPCR of LPS-induced proinflammatory cytokines (Il1b, Il6, Tnf), (ii) LCN2-driven T cell chemotaxis, (iii) FACS-based phenotyping, (iv) FACS-based phagocytosis of pHrodo-labeled E. coli bioparticles, and (v) FACS-based quantification of reactive oxygen species (ROS) using DHR-123. Human plasma samples and post-mortem spleens from three patients with ischemic stroke and one non-stroke control were analyzed for LCN2 expression and cellular localization. Untouched human monocytes from healthy donors were exposed to recombinant LCN2 and assessed by flow cytometry for antigen-presentation, co-stimulatory markers, phagocytosis and ROS production. Results Transcriptomics revealed robust, biphasic splenic Lcn2 upregulation at 24 hours and 7 days after tMCAO. LCN2 localized predominantly to F4/80+ red pulp macrophages (RPMs), and accumulated at RPM-associated CD3+ contact sites. AIS induced a broad suppression of splenic innate and adaptive cytokine networks. Recombinant LCN2 induced T cell hyporesponsiveness, suppressed Il6 and Tnf induction, and impaired CCL5-directed chemotaxis. In monocytes, LCN2 promoted a shift toward Ly6Clow phenotypes, enhanced phagocytosis of E. coli, and uncoupled phagocytosis from ROS production. In human ischemic stroke spleens, LCN2 was detected in CD68+ RPMs and at RPM-associated immune-cell contact sites, consistent with the murine splenic phenotype. In line with the murine findings, human monocytes exposed to LCN2 displayed increased E. coli uptake but reduced ROS, alongside reduced HLA-DR, CD80, CD206, and CD11b expression. Conclusions AIS induces a conserved splenic LCN2-expressing RPM niche in mice and humans. Recombinant LCN2 is sufficient to reprogram T cells and monocytes toward hyporesponsive, tolerogenic and phagocytosis-ROS-uncoupled states, thereby linking cerebral ischemia to systemic immune dysfunction. These findings identify LCN2-expressing RPMs as a translationally relevant immunoregulatory niche after AIS and nominate receptor-specific LCN2 signaling as a candidate pathway for future studies aimed at mitigating post-stroke immunodepression and infection susceptibility without compromising antimicrobial host defense.
ER -