Darmoul D, Rouyer-Fessard C, Blais A, Voisin T, Sapin C, Baricault L, Cibert C, Geraud G, Couvineau A, Laburthe M
Unité de Recherches sur la Différenciation Cellulaire Intestinale, Institut National de la Santé et de la Recherche Médicale (INSERM) U178, Villejuif, France.
Am J Physiol. 1991 Nov;261(5 Pt 1):G763-9. doi: 10.1152/ajpgi.1991.261.5.G763.
The expression of dipeptidyl peptidase IV (DPP IV), an intestinal brush-border hydrolase, has been studied in the rat jejunum crypt-villus axis. DPP IV enzyme activity is lower in crypt cells than in villus cells. Indirect immunofluorescence studies, using a polyclonal antibody raised against purified DPP IV, show a gradient of immunoreactivity from the crypts to the villi that was quantified using confocal laser scanning microscopy. Accordingly, Western blot analysis demonstrates that the steady-state amount of DPP IV is much lower in crypt cells than in villus cells. Northern blot analysis was performed using our cDNA probe for human DPP IV that presents more than 94% homology with rat DPP IV cDNA. Results clearly show that there is approximately seven times less DPP IV mRNA in crypt cells than in villus cells. We conclude that the differentiation-dependent expression of DPP IV in rat jejunum is primarily controlled at the mRNA level.
已在大鼠空肠隐窝 - 绒毛轴中研究了二肽基肽酶IV(DPP IV)的表达,DPP IV是一种肠刷状缘水解酶。隐窝细胞中的DPP IV酶活性低于绒毛细胞。使用针对纯化的DPP IV产生的多克隆抗体进行的间接免疫荧光研究显示,从隐窝到绒毛存在免疫反应性梯度,该梯度使用共聚焦激光扫描显微镜进行了定量。相应地,蛋白质印迹分析表明,隐窝细胞中DPP IV的稳态量远低于绒毛细胞。使用我们的与人DPP IV cDNA具有超过94%同源性的大鼠DPP IV cDNA探针进行了Northern印迹分析。结果清楚地表明,隐窝细胞中的DPP IV mRNA比绒毛细胞中的大约少七倍。我们得出结论,大鼠空肠中DPP IV的分化依赖性表达主要在mRNA水平受到控制。