Targeted disruption of the β-chemokine receptor CCR1 protects against pancreatitis-associated lung injury

Craig Gerard, Jean Louis Frossard, Madhav Bhatia, Ashok Saluja, Norma P. Gerard, Bao Lu, Michael Steer

Research output: Contribution to journalArticle

186 Scopus citations

Abstract

β-Chemokines and their receptors mediate the trafficking and activation of a variety of leukocytes including the lymphocyte and macrophage. An array of no less than eight β-chemokine receptors has been identified, four of which are capable of recognizing the chemokines MIP1α and RANTES. Genetic deletion of one of the MIP1α and RANTES receptors, CCR5, is associated with protection from infection with HIV-1 in humans, while deletion of the ligand MIP1α protects against Coxsackie virus-associated myocarditis. In this report we show that the deletion of another receptor for MIP1α and RANTES, the CCR1 receptor, is associated with protection from pulmonary inflammation secondary to acute pancreatitis in the mouse. The protection from lung injury is associated with decreased levels of TNF-α in a temporal sequence indicating that the activation of the CCR1 receptor is an early event in the systemic inflammatory response syndrome.

Original languageEnglish (US)
Pages (from-to)2022-2027
Number of pages6
JournalJournal of Clinical Investigation
Volume100
Issue number8
DOIs
StatePublished - Oct 15 1997
Externally publishedYes

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Keywords

  • Caerulein
  • Gene deletion
  • MIP1α/RANTES receptor
  • Respiratory distress
  • Systemic immune response syndrome

ASJC Scopus subject areas

  • Medicine(all)

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