Postnatal liver B cell precursors contribute to the establishment of a mature B cell pool in secondary lymphoid organs in mice

The liver contains a diverse repertoire of leukocytes, with liver B cells representing a significant population of hepatic immune cells in both newborns and adults. Despite their importance, these cells remain largely unexplored. In this study, we comprehensively characterized liver B cells from newborns through adulthood in both humans and mice applying a combination of in vivo imaging, immunophenotyping, RNA sequencing, and cell transfer protocols to characterize hepatic B cell subtypes from birth to adulthood. We found that newborn liver B cell population are transcriptionally and phenotypically distinct from those in adults, with significant alterations in genes related to immunoglobulin processing, release, and major histocompatibility complex class I and II functions. Photoconversion-based tracking revealed that liver-resident B cells actively migrate to distant lymphoid organs, including the spleen and bone marrow, where they integrate into the mature immune cell pool. Our findings establish the newborn liver as a crucial niche for B cell maturation and migration, highlighting its role in seeding secondary lymphoid organs and contributing to immune function throughout life. These insights provide new understanding of liver-derived B cells in the postnatal development of the immune system.

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Publication Details

Journal
The Journal of Immunology
Published
2025-10-25
DOI
https://doi.org/10.1093/jimmun/vkaf264
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
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article

Postnatal liver B cell precursors contribute to the establishment of a mature B cell pool in secondary lymphoid organs in mice

Toby B. Lanser, M. Figueroa Pedrosa, Patrick da Silva, Rafael M. Rezende et al.
The Journal of Immunology
Immune Cell Function and Interaction
article

Postnatal liver B cell precursors contribute to the establishment of a mature B cell pool in secondary lymphoid organs in mice

Toby B. Lanser, M. Figueroa Pedrosa, Patrick da Silva, Rafael M. Rezende, Marília Garcia de Oliveira, Bruna Araújo David, Kassiana Mafra, Stephania Libreros, André M. Vale, Brenda Naemi Nakagaki, Wanderson Ferreira da Silva Júnior, Mateus Eustáquio Lopes, Muhammad Usman Babar, Paul Kubes, Maísa Mota Antunes, Cristina Maria Pinto de Paula, Gustavo Batista Menezes, Matheus Silvério Mattos, Ziyu Yang, Antônio Filipe Pereira Caetano, Thiago Mattar Cunha, Gabriel da Rocha Fernandes, Tashi Rastogi, Liza Konnikava
article en

Abstract

The liver contains a diverse repertoire of leukocytes, with liver B cells representing a significant population of hepatic immune cells in both newborns and adults. Despite their importance, these cells remain largely unexplored. In this study, we comprehensively characterized liver B cells from newborns through adulthood in both humans and mice applying a combination of in vivo imaging, immunophenotyping, RNA sequencing, and cell transfer protocols to characterize hepatic B cell subtypes from birth to adulthood. We found that newborn liver B cell population are transcriptionally and phenotypically distinct from those in adults, with significant alterations in genes related to immunoglobulin processing, release, and major histocompatibility complex class I and II functions. Photoconversion-based tracking revealed that liver-resident B cells actively migrate to distant lymphoid organs, including the spleen and bone marrow, where they integrate into the mature immune cell pool. Our findings establish the newborn liver as a crucial niche for B cell maturation and migration, highlighting its role in seeding secondary lymphoid organs and contributing to immune function throughout life. These insights provide new understanding of liver-derived B cells in the postnatal development of the immune system.

The Journal of ImmunologyVol. 215(1)
Universidade Federal de Minas Gerais (BR), Universidade Federal do Rio de Janeiro (BR), Brigham and Women's Hospital (US), Harvard University (US), Instituto Federal de Educação, Ciência e Tecnologia de Minas Gerais (BR), University of Calgary (CA), Universidade de São Paulo (BR), Yale University (US), Czech Academy of Sciences, Institute of Biophysics (CZ), Clinics Hospital of Ribeirão Preto (BR)
Openalex Percentile: Top 68%
Immune Cell Function and Interaction
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