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Heterogeneous expression of toll‐like receptors in lymphatic endothelial cells derived from different tissues
Author(s) -
Garrafa Emirena,
Imberti Luisa,
Tiberio Guido,
Prandini Alberto,
Giulini Stefano Maria,
Caimi Luigi
Publication year - 2011
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1038/icb.2010.111
Subject(s) - chemokine , microbiology and biotechnology , lymphatic endothelium , biology , chemotaxis , lymphatic system , receptor , lymph , cytokine , immunology , inflammation , pathology , medicine , biochemistry
As lymphatic endothelial cells (LECs) express different lymphatic and vascular markers depending on the organ they are derived from, we analysed whether they also show a heterogeneity of response against pathogens. To this end we analysed, for the presence of mRNA encoding for all human toll‐like receptor (TLR), LECs isolated from lymph nodes and thymuses. RNA for TLR1–6 and 9 was identified in thymus‐derived cells, whereas cells derived from lymph nodes contained mRNA for TLR1–4, 6 and 9, but failed to express mRNA specific for TLR5. The differential expression of TLRs was confirmed by the phosphorylation of nuclear factor‐κB p65 only when the two types of LECs were incubated with the appropriate TLR agonists. The stimulation with specific agonists gives rise to a heterogeneous pattern of cytokine and chemokine secretion: thymus‐derived LECs produced preferentially interleukin‐6, interferon‐inducible protein (IP)‐10 and tumour necrosis factor‐α, whereas cells prepared from lymph nodes mainly released interleukin‐8, monocyte chemotactic protein‐1, RANTES and (IP)‐10. Finally, cells purified from lymph nodes expressed a higher level of intercellular adhesion molecule‐1 than did cells prepared from the thymus when stimulated with several TLR agonists. The expression of a large set of TLRs and the responsiveness to specific agonists suggest that LECs are able to respond to pathogens, and the observed differences reflect specialized functions, redundancy and/or roles of LECs of different origin.