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Remodeling of light and dark zone follicular dendritic cells governs germinal center responses

The efficient generation of germinal center (GC) responses requires the directed movement of B cells between distinct microenvironments underpinned by specialized B cell-interacting reticular cells (BRCs). How BRCs are reprogrammed to cater to the developing GC remains unclear and is largely hindere...

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Detalles Bibliográficos
Autores principales: Pikor, Natalia B, Mörbe, Urs, Lütge, Mechthild, Gil-Cruz, Cristina, Perez-Shibayama, Christian, Novkovic, Mario, Cheng, Hung-Wei, Nombela-Arrieta, César, Nagasawa, Takashi, Linterman, Michelle A, Onder, Lucas, Ludewig, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610477/
https://www.ncbi.nlm.nih.gov/pubmed/32424359
http://dx.doi.org/10.1038/s41590-020-0672-y
Descripción
Sumario:The efficient generation of germinal center (GC) responses requires the directed movement of B cells between distinct microenvironments underpinned by specialized B cell-interacting reticular cells (BRCs). How BRCs are reprogrammed to cater to the developing GC remains unclear and is largely hindered by the incomplete resolution of the cellular composition of the B cell follicle. Here, we utilized the genetic targeting of Cxcl13-expressing cells to define the molecular identity of the BRC landscape. Single-cell transcriptomic analysis revealed that BRC subset specification was predetermined in the primary B cell follicle. Further topological remodeling of light and dark zone follicular dendritic cells required the CXCL12-dependent cross-talk with B cells, and dictated GC output by retaining B cells in the follicle and steering their interaction with follicular helper T cells. Together, our results reveal that poised BRC-defined microenvironments establish a feed-forward system that determines the efficacy of the GC reaction.