Differential expression of chemokines in normal pancreas and in chronic pancreatitis
- L Saurer 1, P Reber , T Schaffner , M W Büchler , C Buri , A Kappeler , A Walz , H Friess , C Mueller
- L Saurer 1, P Reber , T Schaffner
- 1Department of Pathology, University of Bern, Bern, Switzerland.
- 0Department of Pathology, University of Bern, Bern, Switzerland.
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View abstract on PubMed
Summary
This summary is machine-generated.Chemokines like MCP-1 are expressed in chronic pancreatitis, recruiting immune cells. Their differential expression suggests a role in disease initiation and progression.
Area Of Science
- Gastroenterology
- Immunology
- Molecular Biology
Background
- Cellular infiltrates are characteristic of early chronic pancreatitis.
- The mechanisms driving immune cell recruitment in this condition remain unclear.
Purpose Of The Study
- To investigate the differential expression of specific chemokine genes in normal and chronic pancreatitis tissues.
- To identify the cellular sources of these chemokines within the pancreas.
Main Methods
- In situ hybridization was used to detect messenger RNA (mRNA) for chemokines (interleukin 8, ENA-78, MIG, MCP-1, I-309).
- Pancreatic tissues from 23 chronic pancreatitis patients and 4 healthy controls were analyzed.
Main Results
- MCP-1 mRNA was found in various cells (ducts, endothelium, macrophages, T cells) in mildly to moderately altered tissues.
- Interleukin 8 and ENA-78 mRNA were primarily in centroacinar ducts of more advanced lesions.
- MIG mRNA was expressed by infiltrating T cells, while I-309 mRNA was present in normal and altered acini.
Conclusions
- Distinct chemokine gene expression patterns were observed in pancreatic parenchyma and infiltrates of chronic pancreatitis patients.
- These findings strongly implicate specific chemokines in the initiation and perpetuation of chronic pancreatitis.
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