Fibroblastic reticular cells form reactive myeloid cell niches in human lymph nodes

Lymph nodes play a key role in maintaining fluid balance in homeostatic and inflamed tissues and provide fibroblastic niche environments for optimal immune cell positioning and interaction. Here, we used single-cell and spatial transcriptomic analyses in combination with high-resolution imaging to molecularly define and functionally characterize niche-forming cells that control inflammation-driven remodeling in human lymph nodes. Fibroblastic reticular cells responded to inflammatory perturbation with activation and expansion of poised niche environments. Inflammation-induced adaptation of lymph node infrastructure and topography included the expansion of peptidase inhibitor 16 (PI16)-expressing reticular cell (PI16<sup>+</sup> RC) networks that enwrap the perivenular conduit system. Interactome analyses indicated that macrophage-derived oncostatin M directs PI16<sup>+</sup> RC activation in inflamed lymph nodes and thereby promotes immune cell aggregation in the perivenular space. In conclusion, these data demonstrate that the inflammatory remodeling of human lymph nodes results in the formation of reactive myeloid cell niches by PI16<sup>+</sup> RCs.

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Publication Details

Journal
Science Immunology
Published
2025-05-02
DOI
https://doi.org/10.1126/sciimmunol.ads6820
Citations
7
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
5.64
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article

Fibroblastic reticular cells form reactive myeloid cell niches in human lymph nodes

Joshua D. Brandstadter, Mechthild Lütge, Mark D. Robinson, Burkhard Ludewig et al.
7 citations
Science Immunology
Single-cell and spatial transcriptomics
5.64
article

Fibroblastic reticular cells form reactive myeloid cell niches in human lymph nodes

Joshua D. Brandstadter, Mechthild Lütge, Mark D. Robinson, Burkhard Ludewig, Lucas Onder, Sandro J. Stoeckli, Ivan Maillard, Angelina De Martin, Hung‐Wei Cheng, Yves Stanossek, Natalia Pikor, Samuel Meili, Lisa Kurz
article en
7 citations

Abstract

Lymph nodes play a key role in maintaining fluid balance in homeostatic and inflamed tissues and provide fibroblastic niche environments for optimal immune cell positioning and interaction. Here, we used single-cell and spatial transcriptomic analyses in combination with high-resolution imaging to molecularly define and functionally characterize niche-forming cells that control inflammation-driven remodeling in human lymph nodes. Fibroblastic reticular cells responded to inflammatory perturbation with activation and expansion of poised niche environments. Inflammation-induced adaptation of lymph node infrastructure and topography included the expansion of peptidase inhibitor 16 (PI16)-expressing reticular cell (PI16<sup>+</sup> RC) networks that enwrap the perivenular conduit system. Interactome analyses indicated that macrophage-derived oncostatin M directs PI16<sup>+</sup> RC activation in inflamed lymph nodes and thereby promotes immune cell aggregation in the perivenular space. In conclusion, these data demonstrate that the inflammatory remodeling of human lymph nodes results in the formation of reactive myeloid cell niches by PI16<sup>+</sup> RCs.

Science ImmunologyVol. 10(107)
SIB Swiss Institute of Bioinformatics (CH), Memorial Sloan Kettering Cancer Center (US), University of Zurich (CH), Board of the Swiss Federal Institutes of Technology (CH), Kantonsspital St. Gallen (CH), ETH Zurich (CH), University Hospital of Zurich (CH), University of Pennsylvania (US)
Industry, innovation and infrastructure
Openalex Percentile: Top 4%
Single-cell and spatial transcriptomics
5.64
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