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Interleukin 1 alpha mRNA-expressing cells on the local inflammatory response in feline infectious peritonitis
1Department of Veterinary Internal Medicine, Faculty of Agriculture, University of Tokyo, Japan.
Insights
Interleukin-1 alpha (IL-1 alpha) mRNA-expressing cells, likely macrophages, were found in feline infectious peritonitis (FIP) lesions. This suggests IL-1 alpha from these cells may contribute to FIP
Area of Science:
- Veterinary Pathology
- Immunology
- Molecular Biology
Background:
- Feline infectious peritonitis (FIP) is a significant disease in cats.
- The role of specific cytokines, like interleukin-1 alpha (IL-1 alpha), in FIP pathogenesis is not fully understood.
Purpose of the Study:
- To investigate the distribution and cellular localization of IL-1 alpha mRNA in tissues affected by FIP.
- To explore the potential role of IL-1 alpha in the inflammatory processes of FIP.
Main Methods:
- In situ hybridization using a biotinylated human IL-1 alpha cDNA probe.
- Examination of tissues from 49 pathologically diagnosed FIP cases.
- Morphological assessment of IL-1 alpha mRNA-expressing cells.
Main Results:
- IL-1 alpha mRNA-expressing cells were identified in various tissues, including peritoneum, lymphoid organs, liver, kidney, and brain.
- Hybridization signals were concentrated in inflammatory lesions on serosal surfaces, particularly in FIP-affected areas.
- The majority of these cells were morphologically consistent with infiltrated macrophages.
Conclusions:
- Macrophages expressing IL-1 alpha mRNA are present in FIP inflammatory lesions.
- IL-1 alpha produced by macrophages at local inflammatory sites may play a role in the development of visceral peritoneal lesions in FIP.
Abstract:
By in situ hybridization with biotinylated human interleukin 1 alpha (IL-1 alpha) cDNA probe, distribution of feline IL-1 alpha mRNA-expressing cells was examined in the tissues from 49 cases diagnosed as feline infectious peritonitis (FIP) by pathological examination. IL-1 alpha mRNA-expressing cells were found in visceral peritoneum, lymphoid organs, liver, kidney, pancreas, digestive tract, lung, pleura, brain, palpebral conjunctiva, and bone marrow. Hybridization signals for IL-1 alpha mRNA were mostly located in the local inflammatory lesions on the serosal surface of various organs and omentum, which were frequently involved in the lesions of FIP (27.8 +/- 5.1 cells/mm2). Morphological examination suggested that they were infiltrated macrophages. However, few IL-1 alpha mRNA-expressing macrophages were in the lesions of other organs. These data suggested that IL-1 alpha produced from macrophages in the local inflammatory sites might participate in the initiation and development of the lesions on the visceral peritoneum in FIP.
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