Lymphatic endothelial cells of the lymph node
Abstract
The influx and efflux of cells and antigens to and from the draining lymph nodes largely take place through the subcapsular, cortical and medullary sinus systems. Recent analyses in mice and humans have revealed unexpected diversity in the lymphatic endothelial cells, which form the distinct regions of the sinuses. As a semipermeable barrier, the lymphatic endothelial cells regulate the sorting of lymph-borne antigens to the lymph node parenchyma and can themselves serve as antigen-presenting cells. The leukocytes entering the lymph node via the sinus system and the lymphocytes egressing from the parenchyma migrate through the lymphatic endothelial cell layer. The sinus lymphatic endothelial cells also orchestrate the organogenesis of lymph nodes, and they undergo bidirectional signalling with other sinus-resident cells, such as subcapsular sinus macrophages, to generate a unique lymphatic niche. In this Review, we consider the structural and functional basis of how the lymph node sinus system coordinates immune responses under physiological conditions, and in inflammation and cancer.
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Small resting T cells pass from the SCS to medullary lymphatic sinuses and gain access to the lymph node at this site.
“From the SCS, small resting T cells pass to medullary lymphatic sinuses and gain access to the lymph node at this site (92–94).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [93]
T cells, B cells, and some neutrophils may leave the lymph node.
“By contrast, T cells, B cells, and some neutrophils may leave the lymph node (93, 95, 96).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [93]
Larger cells such as DCs, macrophages, and activated T cells gain access to the lymph node from the SCS.
“By contrast, larger cells such as DCs, macrophages, and activated T cells gain access to the lymph node from the SCS (92–94).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [93]
T cells exit the lymph node through paracortical sinuses, whereas B cells exit through the SCS and medullary sinuses.
“T cells exit through paracortical sinuses, whereas B cells exit through the SCS and medullary sinuses (93, 96).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [93]
Cites
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Transcytosis route mediates rapid delivery of intact antibodies to draining lymph nodes
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González-Loyola, A., Bovay, E., Kim, J., Lozano, T. W., Sabine, A., Renevey, F., Arroz-Madeira, S., Rapin, A., Wypych, T. P., Rota, G., et al. (2021) · Science Advances · doi:10.1126/sciadv.abf4335 · Cited by 94 · see citing works
Transport and Immune Functions of the Lymphatic System.
Davis, M. J., Zawieja, S. D., & King, P. D. (2025) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022724-104908 · Cited by 42 · see citing works
- Authors
- Jalkanen, S., & Salmi, M.
- Affiliations
- University of Turku (FI)
- Corresponding author
- Salmi, Marko
- Venue
- Nature Reviews Immunology
- Published
- 2020-02-24
- Volume
- 20
- Issue
- 9
- Pages
- 566-578
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W3006851308
- Cited by
- 226
- References
- 5
- Citations by year
- 2026: 26 · 2025: 38 · 2024: 39 · 2023: 39 · 2022: 36 · 2021: 42 · 2020: 6
- FWCI
- 3.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
- Health Sciences › Medicine › Surgery › Lymphatic Disorders and Treatments
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- lymphatic endothelial cells, lymph node sinuses, subcapsular sinus, antigen presentation, lymphocyte migration, subcapsular sinus macrophages, endothelial heterogeneity, lymphadenitis, lymph node cancer
- MeSH terms
- Animals, Endothelium, Lymphatic, Humans, Immunity, Cellular, Inflammation, Lymph Nodes, Neoplasms, Endothelial Cells
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