4.6 Article

Pentraxins: Multifunctional proteins at the interface of innate immunity and inflammation

Journal

BIOFACTORS
Volume 35, Issue 2, Pages 138-145

Publisher

WILEY
DOI: 10.1002/biof.21

Keywords

pentraxin; innate immunity; pattern recognition; apoptotic cells

Funding

  1. European Commission [LSHM-CT-2004-512040, LSHG-CT-2005-005203, LSHP-CT-2003-503240, SP5B-CT-2006-044161]
  2. Telethon [GGP05095]
  3. CARIPLO Foundation
  4. Ministero Universita e Ricerca
  5. University of Milan
  6. Associazione Italiana per la Ricerca sul Cancro Funding Source: Custom

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Pentraxins are a family of multimeric pattern recognition proteins highly conserved in evolution. On the basis of the primary structure of the protomer, pentraxins are divided into two groups: short pentraxins and long pentraxins. C reactive protein, the. first pattern recognition receptor identified, and serum amyloid P component are classic short pentraxins in in the liver in response to IL-6. Long pentraxins, including the prototype PTX3, are expressed in a variety of tissues PTX3 is produced by a variety of cells and tissues, most notably dendritic cells and macrophages, in response. to Toll-like receptor (TLR) engagement and inflammatory cytokines. Through interaction with several ligands, including selected pathogens and apoptotic cells, pentraxins play a role in complement activation-pathogen recognition and apoptotic cell clearance. In addition, PTX3 is involved in the deposition of extracellular matrix and female fertility. Unlike the classic short pentraxins CRP and SAP, PTX3 primary sequence and regulation are highly conserved in in man and mouse. Thus, gene targeting identified PTX3 (and presumably other members of the family) as multifunctional soluble pattern recognition receptors acting as a nonredundant component of the humoral arm of innate immunity and involved in tuning inflammation, matrix deposition, and female fertility. (C) 2009 International Union of Biochemistry and Molecular Biology, Inc. Volume 35, Number 2, March/April 2009, Pages 138-145 . E-mail: alberto.mantovani@humanitas.it.

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