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Updated: Jul 13, 2026

Isolation of Murine Lymph Node Stromal Cells
Published on: August 19, 2014
Subcapsular encounter and complement-dependent transport of immune complexes by lymph node B cells
Tri Giang Phan1, Irina Grigorova, Takaharu Okada
1Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, California 94143, USA.
Insights
Macrophages in lymph nodes rapidly deliver immune complexes to B cells, facilitating antigen capture and immune responses. This highlights a key pathway for B cell-antigen interaction in lymphoid tissues.
Area of Science:
- Immunology
- Cell Biology
- Lymphoid Tissue Dynamics
Background:
- The precise mechanisms governing B cell interactions with antigens within lymphoid tissues remain incompletely elucidated.
- The transport pathways for immune complexes to follicular dendritic cells are not well understood.
Purpose of the Study:
- To investigate the initial events of B cell-antigen encounter in lymph nodes.
- To clarify the role of macrophages and immune complex transport in initiating adaptive immunity.
Main Methods:
- Real-time two-photon microscopy was employed to visualize dynamic cellular interactions in lymph nodes.
- The study focused on the movement and capture of immune complexes by B cells and macrophages.
Main Results:
- Immune complexes were rapidly transported via lymph to subcapsular sinus macrophages.
- B cells captured immune complexes from macrophage extensions in a complement receptor-dependent manner.
- Cognate B cells acquired antigen-containing immune complexes and migrated towards the T zone.
Conclusions:
- Subcapsular sinus macrophages are critical sites for B cell engagement with immune complexes.
- Intrafollicular B cell migration is essential for immune complex transport and cognate antigen recognition, advancing immune surveillance.
Abstract:
The mechanism of B cell-antigen encounter in lymphoid tissues is incompletely understood. It is also unclear how immune complexes are transported to follicular dendritic cells. Here, using real-time two-photon microscopy we noted rapid delivery of immune complexes through the lymph to macrophages in the lymph node subcapsular sinus. B cells captured immune complexes by a complement receptor-dependent mechanism from macrophage processes that penetrated the follicle and transported the complexes to follicular dendritic cells. Furthermore, cognate B cells captured antigen-containing immune complexes from macrophage processes and migrated to the T zone. Our findings identify macrophages lining the subcapsular sinus as an important site of B cell encounter with immune complexes and show that intrafollicular B cell migration facilitates the transport of immune complexes as well as encounters with cognate antigen.
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