Department Pediatric Surgery, Bnai Zion Medical Center, 47 Golomb St., P.O.B. 4940, Haifa 31048, Israel.
Pediatr Res. 2009 Dec;66(6):648-53. doi: 10.1203/PDR.0b013e3181be9f84.
In this study, we examine the responsiveness of intestinal epithelial cell turnover to leptin (LEP) in correlation with leptin receptor (LEPr) expression along the villus-crypt axis in a rat with short bowel syndrome (SBS). Adult rats underwent either a 75% intestinal resection or a transection. SBS-LEP rats underwent bowel resection and were treated with LEP starting from the fourth postoperative day. Parameters of intestinal adaptation, enterocyte proliferation, and enterocyte apoptosis were determined at sacrifice. RT-PCR technique was used to determine Bax and Bcl-2 gene expression in ileal mucosa. Villus tips, lateral villi, and crypts were separated using laser capture microdissection. LEPr expression for each compartment was assessed by quantitative real-time PCR (Taqman). Treatment with LEP significantly stimulated all parameters of adaptation. LEPr expression in crypts significantly increased in SBS rats (vs Sham rats) and was accompanied by a significant increase in enterocyte proliferation and decreased apoptosis after LEP administration. A significant increase in LEPr expression at the tip of the villus in SBS rats was accompanied by decreased cell apoptosis. In conclusion LEP accelerated enterocyte turnover and stimulated intestinal adaptation. The effect of LEP on enterocyte proliferation and enterocyte apoptosis correlated with receptor expression along the villus-crypt axis.
在这项研究中,我们研究了短肠综合征(SBS)大鼠中,肠上皮细胞更新对瘦素(LEP)的反应性与绒毛-隐窝轴上瘦素受体(LEPr)表达的相关性。成年大鼠接受了 75%的肠切除术或横断术。SBS-LEP 大鼠接受肠切除,并从术后第四天开始接受 LEP 治疗。在牺牲时确定了肠道适应、肠细胞增殖和肠细胞凋亡的参数。使用 RT-PCR 技术测定回肠黏膜中 Bax 和 Bcl-2 基因的表达。使用激光捕获显微切割分离绒毛尖端、侧绒毛和隐窝。通过定量实时 PCR(Taqman)评估每个隔室的 LEPr 表达。LEP 的治疗显著刺激了所有适应参数。SBS 大鼠(与 Sham 大鼠相比)中隐窝中的 LEPr 表达显著增加,LEP 给药后肠细胞增殖显著增加,凋亡减少。SBS 大鼠绒毛尖端 LEPr 表达的显著增加伴随着细胞凋亡的减少。总之,LEP 加速了肠细胞的更替并刺激了肠道适应。LEP 对肠细胞增殖和肠细胞凋亡的影响与绒毛-隐窝轴上的受体表达相关。