人小肠可吸收上皮细胞与不可吸收性上皮细胞的分子学特点

来源 :世界核心医学期刊文摘(胃肠病学分册) | 被引量 : 0次 | 上传用户:purple601
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Background and aims:Perturbation of differentiation of the crypt-villus axis of the human small intestine is associated with several intestinal disorders of clinical importance.At present,differentiation of small intestinal enterocytes in the crypt-villus axis is not well characterised.Subjects and methods:Expression profiling of microdissected enterocytes lining the upper part of crypts or the middle of villi was performed using the Affymetrix X3P arrays and several methods for confirmation.Results:A total of 978 differentially expressed sequences representing 778 unique UniGene IDs were found and categorised into four functional groups.In enterocytes lining the upper part of crypts,cell cycle promoting genes and transcription/translation related genes were predominantly expressed,whereas in enterocytes lining the middle of villi,high expression of cell cycle inhibiting genes,metabolism related genes,and vesicle/transport related genes was found.Conclusion:Two types or enterocytes were dissected at the molecular level,the nonabsorptive enterocyte located in the upper part of crypts and the absorptive enterocyte found in the middle of villi.These data improve our knowledge about the physiology of the crypt-villus architecture in human small intestine and provide new insights into pathophysiological phenomena,such as villus atrophy,which is clinically important. Background and aims: Perturbation of differentiation of the crypt-villus axis of the human small intestine is associated with several intestinal disorders of clinical importance. At present, differentiation of small intestinal enterocytes in the crypt-villus axis is not well-characterized. Subjects and methods : Expression profiling of microdissected enterocytes lining the upper part of crypts or the middle of villi was performed using the Affymetrix X3 P arrays and several methods for confirmation. Results: A total of 978 differentially expressed sequences representing 778 unique UniGene IDs were found and categorized into four functional groups.In enterocytes lining the upper part of crypts, cell cycle promoting genes and transcription / translation related genes were predominantly expressed, but in in cells lining the middle of villi, high expression of cell cycle inhibiting genes, metabolism related genes, and vesicle / transport related genes was found. Confluence: Two types or enterocytes wer e dissected at the molecular level, the nonabsorptive enterocyte located in the upper part of crypts and the absorptive enterocyte found in the middle of villi.These data improve our knowledge about the physiology of the crypt-villus architecture in human small intestine and provide new insights into pathophysiological phenomena, such as villus atrophy, which is clinically important.
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