| Literature DB >> 10627389 |
Abstract
Chicken monocytes and a macrophage-like cell line were used to determine the presence of macrophage inflammatory protein-1 beta (MIP-1 beta). RNA was extracted from these cells and subjected to reverse transcription with an anti-sense primer specific for the whole length of the MIP-1 beta cDNA. After a polymerase chain reaction to amplify the cDNA, a 200 bp gene product was detected, which corresponded to the molecular weight of the MIP-1 beta. The culture supernate of these cells did not have the ability to attract heterophils. However, after infection with Mycoplasma gallisepticum, a potent chemotactic substance in the culture supernate was detected. The chemotactic activity could be neutralized by antibodies prepared against two 10-amino-acid peptides of MIP-1 beta, indicating that the substance was MIP-1 beta. Copyright 2000 Harcourt Publishers Ltd.Entities:
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Year: 2000 PMID: 10627389 DOI: 10.1053/jcpa.1999.0340
Source DB: PubMed Journal: J Comp Pathol ISSN: 0021-9975 Impact factor: 1.311