ADEQUACY OF MUCOSAL BIOPSIES FOR EVALUATION OF INTESTINAL CYTOKINE-SPECIFIC MESSENGER-RNA - COMPARATIVE-STUDY OF RT-PCR IN BIOPSIES AND ISOLATED CELLS FROM NORMAL AND INFLAMED INTESTINE

被引:20
作者
FUKUSHIMA, K [1 ]
WEST, G [1 ]
FIOCCHI, C [1 ]
机构
[1] CASE WESTERN RESERVE UNIV,SCH MED,DIV GASTROENTEROL,CLEVELAND,OH 44106
关键词
ULCERATIVE COLITIS; CROHNS DISEASE; INFLAMMATORY BOWEL DISEASE; INTERLEUKIN-BETA; INTERLEUKIN-2; QUANTITATIVE REVERSE TRANSCRIPTION-POLYMERASE CHAIN REACTION; BIOPSY;
D O I
10.1007/BF02285198
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Endoscopic biopsies are being increasingly utilized to investigate cytokine profiles in normal and diseased intestine. To evaluate the adequacy of mucosal biopsies as a source of cytokine-specific mRNA, we measured their content of interleukin-1 beta (IL-1 beta) and interleukin-2 (IL-2) mRNA by reverse transcription-polymerase chain reaction and compared it to that of autologous lamina propria mononuclear cells in control and inflammatory bowel disease-involved specimens. High-quality total RNA was recovered more consistently from cell isolates than from biopsies. Interleukin-1 beta mRNA was reliably detected in both cell and biopsy samples, whereas IL-2 mRNA was measurable in all lamina propria cells but not always in biopsies. Compared to controls, levels of IL-1 beta were significantly elevated in Crohn's disease and ulcerative colitis cells and biopsies, and a weak but significant correlation existed between values derived from the two sources. In contrast, only ulcerative colitis cell isolates but not biopsies contained significantly reduced concentrations of IL-2 mRNA compared to those of control and Crohn's disease samples, and no correlation was found between cell and biopsy contents. Widely different levels of cytokine-specific mRNA were present in closely adjacent biopsies, particularly for IL-2. These results suggest that mucosal biopsies are suitable to assess some but not all cytokine-specific mRNA due to variation in RNA recovery, intrinsic level of cytokine gene expression, and substantial variability of cytokine transcripts.
引用
收藏
页码:1498 / 1505
页数:8
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