Regulation of leukocyte recruitment by the long pentraxin PTX3 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-04

AUTHORS

Livija Deban, Remo Castro Russo, Marina Sironi, Federica Moalli, Margherita Scanziani, Vanessa Zambelli, Ivan Cuccovillo, Antonio Bastone, Marco Gobbi, Sonia Valentino, Andrea Doni, Cecilia Garlanda, Silvio Danese, Giovanni Salvatori, Marica Sassano, Virgilio Evangelista, Barbara Rossi, Elena Zenaro, Gabriela Constantin, Carlo Laudanna, Barbara Bottazzi, Alberto Mantovani

ABSTRACT

Pentraxins are a superfamily of conserved proteins involved in the acute-phase response and innate immunity. Pentraxin 3 (PTX3), a prototypical member of the long pentraxin subfamily, is a key component of the humoral arm of innate immunity that is essential for resistance to certain pathogens. A regulatory role for pentraxins in inflammation has long been recognized, but the underlying mechanisms remain unclear. Here we report that PTX3 bound P-selectin and attenuated neutrophil recruitment at sites of inflammation. PTX3 released from activated leukocytes functioned locally to dampen neutrophil recruitment and regulate inflammation. Antibodies have glycosylation-dependent regulatory effect on inflammation. Therefore, PTX3, which is an essential component of humoral innate immunity, and immunoglobulins share functional outputs, including complement activation, opsonization and, as shown here, glycosylation-dependent regulation of inflammation. More... »

PAGES

328

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ni.1854

DOI

http://dx.doi.org/10.1038/ni.1854

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1048981069

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20208538


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