Yeh K Y, Yeh M, Glass J
Department of Medicine, Feist-Weiller Cancer Center, Louisiana State University Medical Center, Shreveport, Louisiana 71130, USA.
Am J Physiol. 1998 Sep;275(3):G572-83. doi: 10.1152/ajpgi.1998.275.3.G572.
Jejunal expression of three brush-border membrane (BBM) enzymes, intestinal alkaline phosphatase (IAP), lactose-phlorizin hydrolase (LPH), and sucrase-isomaltase (SI), and a cytosolic protein, ferritin (Ft), was investigated after transient segmental ischemia-reperfusion (I/R). I/R reduced mucosal IAP, LPH, and SI mRNAs to 36%, 11%, and 38% of normal jejunal levels after 3 h of reperfusion and to 22%, 8%, and 51% of normal jejunal levels after 6 h of reperfusion, respectively. Intriguingly, in the internal control jejunum IAP and LPH mRNAs also decreased significantly. LPH and SI mRNA rapidly recovered to levels significantly higher than those of normal jejunum at 12 h, whereas IAP mRNA levels did not recover until 48 h. Enzyme activity paralleled changes in mRNA levels in the ischemic reperfused jejunum. Electrophoretic mobility shift assays showed that I/R significantly increased SI footprinting 1 (SIF1) binding activity. The mobility of one of the DNA-protein complexes was further retarded in the presence of anti-Cdx-2 antibody, suggesting that either Cdx-2 or a related protein was interacting with the SIF1 sequences. Similar to BBM enzymes, cytosolic Ft mRNA and protein were significantly decreased at 3 and 6 h after I/R. By 12 h, Ft mRNA, but not Ft protein, had increased to higher than normal levels. We conclude that a rapid recovery of BBM mRNAs and enzymes occurs in regenerating mucosa after upper villus damage. The increase of SIF1 binding protein activity after I/R may enhance SI, and perhaps LPH, gene transcription. The expression of Ft is regulated at both pretranslational and translational levels.
在短暂性节段性缺血再灌注(I/R)后,研究了空肠中三种刷状缘膜(BBM)酶,即肠碱性磷酸酶(IAP)、乳糖-根皮苷水解酶(LPH)和蔗糖酶-异麦芽糖酶(SI)以及一种胞质蛋白铁蛋白(Ft)的表达情况。再灌注3小时后,I/R使黏膜IAP、LPH和SI mRNA分别降至正常空肠水平的36%、11%和38%;再灌注6小时后,分别降至正常空肠水平的22%、8%和51%。有趣的是,在内部对照空肠中,IAP和LPH mRNA也显著下降。LPH和SI mRNA在12小时时迅速恢复到显著高于正常空肠的水平,而IAP mRNA水平直到48小时才恢复。酶活性与缺血再灌注空肠中mRNA水平的变化平行。电泳迁移率变动分析表明,I/R显著增加了SI足迹1(SIF1)结合活性。在抗Cdx-2抗体存在的情况下,一种DNA-蛋白质复合物的迁移率进一步减慢,表明Cdx-2或一种相关蛋白正在与SIF1序列相互作用。与BBM酶类似,I/R后3小时和6小时胞质Ft mRNA和蛋白显著下降。到12小时时,Ft mRNA升高到高于正常水平,但Ft蛋白未升高。我们得出结论,在上部绒毛损伤后再生的黏膜中,BBM mRNA和酶会迅速恢复。I/R后SIF1结合蛋白活性的增加可能会增强SI,也许还有LPH的基因转录。Ft的表达在转录前和翻译水平均受到调控。