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Vitronectin

Su, Yu Ching and Riesbeck, Kristian LU orcid (2017) p.351-360
Abstract

The multifaceted complement regulator vitronectin (Vn) can be found in almost all tissues of the human body. It is primarily produced by the liver and is thus detected at high concentrations in plasma. Upon inflammation, Vn is upregulated revealing its importance for the innate immune defence against danger signals. It consists of 459 amino acids and has several key sequences linked to its functions. Vn interacts at its N-terminal with plasminogen activator inhibitor-1 and urokinase-type plasminogen activator receptor (uPAR). Downstream of these binding sites are sequences that attract integrins and collagen in addition to the thrombin-antithrombin III complex. Heme-binding plasma proteins, as well as plasminogen, can also interact with... (More)

The multifaceted complement regulator vitronectin (Vn) can be found in almost all tissues of the human body. It is primarily produced by the liver and is thus detected at high concentrations in plasma. Upon inflammation, Vn is upregulated revealing its importance for the innate immune defence against danger signals. It consists of 459 amino acids and has several key sequences linked to its functions. Vn interacts at its N-terminal with plasminogen activator inhibitor-1 and urokinase-type plasminogen activator receptor (uPAR). Downstream of these binding sites are sequences that attract integrins and collagen in addition to the thrombin-antithrombin III complex. Heme-binding plasma proteins, as well as plasminogen, can also interact with Vn through heparin-binding domains. One of the main functions of Vn is to inhibit the terminal pathway of the complement system by preventing formation of the lethal pore-forming complex. This chapter will in detail discuss the knowledge on this important molecule.

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Please use this url to cite or link to this publication:
author
and
organization
publishing date
type
Chapter in Book/Report/Conference proceeding
publication status
published
subject
keywords
Cell adhesion, Complement regulator, Haemostasis, Heparin, Integrin, Multimeric, Plasminogen, Vitronectin
host publication
The Complement FactsBook : Second Edition - Second Edition
pages
10 pages
publisher
Elsevier
external identifiers
  • scopus:85041270026
ISBN
9780128104200
DOI
10.1016/B978-0-12-810420-0.00033-X
language
English
LU publication?
yes
id
c210ca20-2425-4d7a-bf54-f10336580064
date added to LUP
2018-02-12 14:23:12
date last changed
2022-05-03 01:11:00
@inbook{c210ca20-2425-4d7a-bf54-f10336580064,
  abstract     = {{<p>The multifaceted complement regulator vitronectin (Vn) can be found in almost all tissues of the human body. It is primarily produced by the liver and is thus detected at high concentrations in plasma. Upon inflammation, Vn is upregulated revealing its importance for the innate immune defence against danger signals. It consists of 459 amino acids and has several key sequences linked to its functions. Vn interacts at its N-terminal with plasminogen activator inhibitor-1 and urokinase-type plasminogen activator receptor (uPAR). Downstream of these binding sites are sequences that attract integrins and collagen in addition to the thrombin-antithrombin III complex. Heme-binding plasma proteins, as well as plasminogen, can also interact with Vn through heparin-binding domains. One of the main functions of Vn is to inhibit the terminal pathway of the complement system by preventing formation of the lethal pore-forming complex. This chapter will in detail discuss the knowledge on this important molecule.</p>}},
  author       = {{Su, Yu Ching and Riesbeck, Kristian}},
  booktitle    = {{The Complement FactsBook : Second Edition}},
  isbn         = {{9780128104200}},
  keywords     = {{Cell adhesion; Complement regulator; Haemostasis; Heparin; Integrin; Multimeric; Plasminogen; Vitronectin}},
  language     = {{eng}},
  month        = {{10}},
  pages        = {{351--360}},
  publisher    = {{Elsevier}},
  title        = {{Vitronectin}},
  url          = {{http://dx.doi.org/10.1016/B978-0-12-810420-0.00033-X}},
  doi          = {{10.1016/B978-0-12-810420-0.00033-X}},
  year         = {{2017}},
}