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Characterization of CD41+ cells in the lymph node

Authors :
Li Dai
Mayuko Uehara
Xiaofei Li
Brenna A. LaBarre
Naima Banouni
Takaharu Ichimura
Melissa M. Lee-Sundlov
Vivek Kasinath
Jade A. Sullivan
Heyu Ni
Francesca Barone
Silvia Giannini
Baharak Bahmani
Peter T. Sage
Nikolaos A. Patsopoulos
George C. Tsokos
Jonathan S. Bromberg
Karin Hoffmeister
Liwei Jiang
Reza Abdi
Source :
Frontiers in Immunology, Vol 13 (2022)
Publication Year :
2022
Publisher :
Frontiers Media S.A., 2022.

Abstract

Lymph nodes (LNs) are the critical sites of immunity, and the stromal cells of LNs are crucial to their function. Our understanding of the stromal compartment of the LN has deepened recently with the characterization of nontraditional stromal cells. CD41 (integrin αIIb) is known to be expressed by platelets and hematolymphoid cells. We identified two distinct populations of CD41+Lyve1+ and CD41+Lyve1- cells in the LNs. CD41+Lyve1- cells appear in the LN mostly at the later stages of the lives of mice. We identified CD41+ cells in human LNs as well. We demonstrated that murine CD41+ cells express mesodermal markers, such as Sca-1, CD105 and CD29, but lack platelet markers. We did not observe the presence of platelets around the HEVs or within proximity to fibroblastic reticular cells of the LN. Examination of thoracic duct lymph fluid showed the presence of CD41+Lyve1- cells, suggesting that these cells recirculate throughout the body. FTY720 reduced their trafficking to lymph fluid, suggesting that their egress is controlled by the S1P1 pathway. CD41+Lyve1- cells of the LNs were sensitive to radiation, suggestive of their replicative nature. Single cell RNA sequencing data showed that the CD41+ cell population in naïve mouse LNs expressed largely stromal cell markers. Further studies are required to examine more deeply the role of CD41+ cells in the function of LNs.

Details

Language :
English
ISSN :
16643224
Volume :
13
Database :
Directory of Open Access Journals
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.3dc4347bd1d44db88e9d3b536cdd3e39
Document Type :
article
Full Text :
https://doi.org/10.3389/fimmu.2022.801945