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J Exp Med. 2019 Jul 19. pii: jem.20181705. doi: 10.1084/jem.20181705. [Epub ahead of print]

Embryonic FAP+ lymphoid tissue organizer cells generate the reticular network of adult lymph nodes.

Author information

1
Lymphocyte Signaling and Development, Babraham Institute, Cambridge, UK alice.denton@babraham.ac.uk.
2
Department of Medicine, University of Cambridge, Cambridge, UK.
3
Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
4
Lymphocyte Signaling and Development, Babraham Institute, Cambridge, UK.
5
Weill Cornell Medicine and Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.

Abstract

The induction of adaptive immunity is dependent on the structural organization of LNs, which is in turn governed by the stromal cells that underpin LN architecture. Using a novel fate-mapping mouse model, we trace the developmental origin of mesenchymal LN stromal cells (mLNSCs) to a previously undescribed embryonic fibroblast activation protein-α (FAP)+ progenitor. FAP+ cells of the LN anlagen express lymphotoxin β receptor (LTβR) and vascular cell adhesion molecule (VCAM), but not intercellular adhesion molecule (ICAM), suggesting they are early mesenchymal lymphoid tissue organizer (mLTo) cells. Clonal labeling shows that FAP+ progenitors locally differentiate into mLNSCs. This process is also coopted in nonlymphoid tissues in response to infection to facilitate the development of tertiary lymphoid structures, thereby mimicking the process of LN ontogeny in response to infection.

PMID:
31324739
DOI:
10.1084/jem.20181705

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