Interleukin 1 and interleukin 1β converting enzyme (caspase 1) expression in the human colonic epithelial barrier.: Caspase 1 downregulation in colon cancer

被引:52
作者
Jarry, A
Vallette, G
Cassagnau, E
Moreau, A
Bou-Hanna, C
Lemarre, P
Letessier, E
Le Neel, JC
Galmiche, JP
Laboisse, CL
机构
[1] CHU Nantes, Fac Med, INSERM, CJF 9404, F-44035 Nantes 01, France
[2] CHU Nantes, Serv Anat Pathol, F-44035 Nantes, France
[3] CHU Nantes, Chirurg Clin A, F-44035 Nantes 01, France
[4] CHU Nantes, Serv Hepatogastroenterol, F-44035 Nantes 01, France
关键词
caspase; 1; colonic epithelial cells; colon cancer; interleukin; interleukin 1 beta converting enzyme;
D O I
10.1136/gut.45.2.246
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Interleukin (IL) 1 beta converting enzyme (now known as caspase 1) is able to process pro-IL-1 beta into its active form and is involved in proapoptotic signalling. Aims-To characterise IL-1 and caspase 1 expression in human colonic epithelial cells. Methods-Intracellular IL-1 content (IL-1 alpha and IL-1 beta) was measured by ELISA in freshly isolated human normal colonocytes. Caspase 1 expression was determined both at the mRNA level using in situ hybridisation and reverse transcription polymerase chain reaction, and at the protein level by immunoblotting experiments using antibodies specific for the preform of caspase 1 and for its cleavage forms. Results-Low amounts of IL-1 beta were found in nearly all preparations (92%), and IL-1 alpha was detected in only 45% of human colonocyte preparations. The normal colonic epithelium strongly expressed caspase 1, both at the mRNA level and at the protein level in its latent form. In contrast, caspase 1 was not expressed in colon cancer (primary colonic adenocarcinomas and cancer cell lines). Conclusions-The demonstration that the human colonic epithelial barrier is able to express caspase 1 and its substrate IL-1 beta reinforces the concept that, under certain conditions, the epithelium could trigger an inflammatory reaction. In addition, the finding that caspase 1 was downregulated in colonic adenocarcinomas supports the concept that disrupted apoptosis pathways may be involved in tumour formation and/or may confer resistance to treatment.
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页码:246 / 251
页数:6
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