Follicular Dendritic Cells Emerge from Ubiquitous Perivascular Precursors
Author(s) -
Nike Julia Kräutler,
Veronika Kana,
Jan Kranich,
Yinghua Tian,
Dushan Perera,
Doreen Lemm,
Petra Schwarz,
Annika Armulik,
Jeffrey L. Browning,
Michelle D. Tallquist,
Thorsten Buch,
José B. Oliveira-Martins,
Caihong Zhu,
Mario Hermann,
Ulrich Wagner,
Robert Brink,
Mathias Heikenwälder,
Adriano Aguzzi
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.05.032
Subject(s) - biology , follicular dendritic cells , follicular phase , microbiology and biotechnology , dendritic cell , perivascular space , immunology , anatomy , endocrinology , immune system , antigen presenting cell , t cell
The differentiation of follicular dendritic cells (FDC) is essential to the remarkable microanatomic plasticity of lymphoid follicles. Here we show that FDC arise from ubiquitous perivascular precursors (preFDC) expressing platelet-derived growth factor receptor β (PDGFRβ). PDGFRβ-Cre-driven reporter gene recombination resulted in FDC labeling, whereas conditional ablation of PDGFRβ(+)-derived cells abolished FDC, indicating that FDC originate from PDGFRβ(+) cells. Lymphotoxin-α-overexpressing prion protein (PrP)(+) kidneys developed PrP(+) FDC after transplantation into PrP(-) mice, confirming that preFDC exist outside lymphoid organs. Adipose tissue-derived PDGFRβ(+) stromal-vascular cells responded to FDC maturation factors and, when transplanted into lymphotoxin β receptor (LTβR)(-) kidney capsules, differentiated into Mfge8(+)CD21/35(+)FcγRIIβ(+)PrP(+) FDC capable of trapping immune complexes and recruiting B cells. Spleens of lymphocyte-deficient mice contained perivascular PDGFRβ(+) FDC precursors whose expansion required both lymphoid tissue inducer (LTi) cells and lymphotoxin. The ubiquity of preFDC and their strategic location at blood vessels may explain the de novo generation of organized lymphoid tissue at sites of lymphocytic inflammation.
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