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Fate mapping and scRNA sequencing reveal origin and diversity of lymph node stromal precursors.

Authors :
Lenti E
Genovese L
Bianchessi S
Maurizio A
Sain SB
di Lillo A
Mattavelli G
Harel I
Bernassola F
Hehlgans T
Pfeffer K
Crosti M
Abrignani S
Evans SM
Sitia G
GuimarĂ£es-Camboa N
Russo V
van de Pavert SA
Garcia-Manteiga JM
Brendolan A
Source :
Immunity [Immunity] 2022 Apr 12; Vol. 55 (4), pp. 606-622.e6. Date of Electronic Publication: 2022 Mar 30.
Publication Year :
2022

Abstract

Lymph node (LN) stromal cells play a crucial role in LN development and in supporting adaptive immune responses. However, their origin, differentiation pathways, and transcriptional programs are still elusive. Here, we used lineage-tracing approaches and single-cell transcriptome analyses to determine origin, transcriptional profile, and composition of LN stromal and endothelial progenitors. Our results showed that all major stromal cell subsets and a large proportion of blood endothelial cells originate from embryonic Hoxb6 <superscript>+</superscript> progenitors of the lateral plate mesoderm (LPM), whereas lymphatic endothelial cells arise from Pax3 <superscript>+</superscript> progenitors of the paraxial mesoderm (PXM). Single-cell RNA sequencing revealed the existence of different Cd34 <superscript>+</superscript> and Cxcl13 <superscript>+</superscript> stromal cell subsets and showed that embryonic LNs contain proliferating progenitors possibly representing the amplifying populations for terminally differentiated cells. Taken together, our work identifies the earliest embryonic sources of LN stromal and endothelial cells and demonstrates that stromal diversity begins already during LN development.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4180
Volume :
55
Issue :
4
Database :
MEDLINE
Journal :
Immunity
Publication Type :
Academic Journal
Accession number :
35358427
Full Text :
https://doi.org/10.1016/j.immuni.2022.03.002