Expression of Monocyte Chemotactic Protein-1 and Macrophage Inflammatory Protein-1alpha in Intraabdominal Abscess Induced by Bacteroides fragilis Infection.
- Author:
Jung Mogg KIM
1
;
Seo Gue YOON
;
Young Jeon KIM
;
Yang Ja CHO
Author Information
1. Department of Microbiology, Hanyang University College of Medicine, Korea.
- Publication Type:Original Article
- Keywords:
B. fragilis;
fibroblast;
intraabdominal abscess;
MCP-1;
MIP-1alpha
- MeSH:
Abscess*;
Animals;
Bacteria;
Bacteroides fragilis*;
Bacteroides*;
Chemokine CCL2*;
Chemokine CCL3;
Chemokines;
Cytokines;
Enzyme-Linked Immunosorbent Assay;
Fibroblasts;
Guanidine;
Intraabdominal Infections;
Macrophages*;
Mice;
Models, Theoretical;
Monocytes*;
Neutrophils;
RNA;
RNA, Messenger;
Sepsis;
Silicon Dioxide;
Tissue Extracts;
Tumor Necrosis Factor-alpha
- From:Journal of the Korean Society for Microbiology
1997;32(2):201-212
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: Bacteroides fragilis is the most frequently isolated anaerobes in tissue of intraabdominal infection, particularly in intraabdominal sepsis or abscess. In acute experimental model with an intraabdominal infection, the response to B. fragilis is characterized by infiltration of neutrophils and monocytes. To understand the pathogenesis of B. fragilis infection, it is important to explore the mechanism for inflammatory signals such as chemokines induced by this bacteria. The goal of this study was to determine whether peritoneal monocytes or fibroblasts surrounding with intraabdominal abscess induced by B. fragilis could express chemokines such as monocyte chemotactic protein-1 (MCP-1) or macrophage inflammatory protein-1a (MIP-1a). METHODS: 1) After C57BL/6 mice were intraperitoneally inoculated with abscess-inducing agents containing B. fragilis, RNA was extracted from the intraperitoneal tissues of the mice using Ottawa sand and the guanidinium thiocyanate-phenol-chloroform method in 3 days later. 2) After C57BL/6 mouse peritoneal monocytes were infected with B. fragilis for 1, 4 and 9 hours, cellular RNA was extracted from the cells. 3) Fibroblasts isolated from intraabdominal abscess nodules induced by B. fragilis infection were growth in tissue culture for 3 to 4 weeks. After the fibroblasts were stimulated with IL-1alpha (0.1-10 ng/ml) or TNFalpha (0.1-10 ng/ml) for 24 hours, total cellular RNA was extracted. MCP-1 or MIP-1alpha mRNA expression was assessed using RTPCR. MCP-1 or MIP-1alpha proteins in cluture supernatants or tissue extracts were also measured by ELISA. RESULTS: 1) MCP-1 or MIP-1alpha mRNA was highly expressed in peritoneal tissue of C57BL/6 mice bearing with intraabdominal abscess induced by B. fragilis. 2) Expression of MCP-1 mRNA increased at 9 hours in mouse peritoneal monocytes infected with B. fragilis. MIP-1alpha mRNA was initially expressed and perisisted in the monocytes infected with B. fragilis for 9 hours. MCP-1 or MIP-1alpha proteins was also parallel to the expression of those chemokines. 3) The fibroblasts isolated from intraabdominal abscess nodules by B. fragilis infection constitutively expressed MCP-1, MIP-1alpha, production in the fibroblasts was significantly upregulated in response to proinflammatory cytokines produced in the monocytes, including IL-1alpha and TNFalpha, but MCP-1 production were not. The normal fibroblasts from uninfected mice didnot show significant production of MCP-1 or MIP-1a in response to IL-1a or TNFalpha. CONCLUSION: These results suggest that peritoneal monocytes and fibroblasts surrounding with abscesses induced by B. fragilis produce MCP-1 or MIP-1a. Furthermore, it could be extrapolated that those effects may play a role in the formation of intraabdominal abscess nodules.
