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Possible participation of macrophage inflammatory protein 2 in neutrophil infiltration in allergic inflammation in rats.

Abstract
Recombinant rat macrophage inflammatory protein 2 (MIP-2) was prepared from E. coli transfected with a glutathione-S-transferase (GST)-MIP-2 fusion protein expression vector. A polyclonal antibody to rat MIP-2 was then obtained from rabbits by immunization with recombinant rat MIP-2. Using the polyclonal antibody which selectively suppressed neutrophil chemotactic activity of MIP-2, the role of MIP-2 in neutrophil infiltration in allergic inflammation in rats was studied. In an air pouch-type allergic inflammation model in rats, neutrophil infiltration into the pouch fluid increased with time after antigen challenge. Neutrophil chemotactic activity in the pouch fluid collected 8 h after antigen challenge was diminished by anti-MIP-2 antibody. In addition, when leukocytes that had infiltrated into the pouch fluid collected 4 h after antigen challenge were incubated, neutrophil chemotactic activity in the conditioned medium increased time-dependently, and the activity was neutralized by anti-MIP-2 antibody. Furthermore, when anti-MIP-2 antibody was injected into the pouch 6 h after antigen challenge, neutrophil infiltration into the pouch fluid during the next 2 h was suppressed. These findings indicate that MIP-2 plays an important role in neutrophil infiltration in rat allergic inflammation.
AuthorsY Q Xiao, J I Tanabe, T Edamatsu, N Hirasawa, S Mue, K Ohuchi
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 1361 Issue 2 Pg. 138-46 (Aug 22 1997) ISSN: 0006-3002 [Print] Netherlands
PMID9300795 (Publication Type: Journal Article)
Chemical References
  • Antibodies
  • Chemokine CXCL2
  • Chemotactic Factors
  • Monokines
  • Recombinant Proteins
Topics
  • Amino Acid Sequence
  • Animals
  • Antibodies (administration & dosage, immunology)
  • Antigen-Antibody Reactions
  • Body Fluids (immunology)
  • Cheek
  • Chemokine CXCL2
  • Chemotactic Factors (administration & dosage, immunology)
  • Cloning, Molecular
  • Hypersensitivity, Immediate (immunology, physiopathology)
  • Inflammation (immunology, physiopathology)
  • Molecular Sequence Data
  • Monokines (administration & dosage, immunology)
  • Neutrophils (physiology)
  • Rats
  • Recombinant Proteins (immunology)

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