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本文引用的文献

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Prostaglandin E2 induces the expression of IL-1alpha in colon cancer cells.前列腺素E2诱导结肠癌细胞中白细胞介素-1α的表达。
J Immunol. 2007 Apr 1;178(7):4097-103. doi: 10.4049/jimmunol.178.7.4097.
2
Forskolin: from an ayurvedic remedy to a modern agent.福司可林:从印度草药到现代药物。
Planta Med. 1985 Dec;51(6):473-7. doi: 10.1055/s-2007-969566.
3
Wnt/beta-catenin signaling in development and disease.发育与疾病中的Wnt/β-连环蛋白信号通路
Cell. 2006 Nov 3;127(3):469-80. doi: 10.1016/j.cell.2006.10.018.
4
Regulation of amphiregulin and epiregulin expression in human colonic subepithelial myofibroblasts.人结肠上皮下肌成纤维细胞中双调蛋白和表皮调节素表达的调控
Int J Mol Med. 2006 Sep;18(3):497-503.
5
Roles of myofibroblasts in prostaglandin E2-stimulated intestinal epithelial proliferation and angiogenesis.肌成纤维细胞在前列腺素E2刺激的肠上皮增殖和血管生成中的作用。
Cancer Res. 2006 Jan 15;66(2):846-55. doi: 10.1158/0008-5472.CAN-05-2606.
6
The prostaglandin E2 receptor EP2 is required for cyclooxygenase 2-mediated mammary hyperplasia.环氧化酶2介导的乳腺增生需要前列腺素E2受体EP2。
Cancer Res. 2005 Jun 1;65(11):4496-9. doi: 10.1158/0008-5472.CAN-05-0129.
7
Amphiregulin: an early trigger of liver regeneration in mice.双调蛋白:小鼠肝脏再生的早期触发因子。
Gastroenterology. 2005 Feb;128(2):424-32. doi: 10.1053/j.gastro.2004.11.006.
8
Prostaglandin E2 reduces radiation-induced epithelial apoptosis through a mechanism involving AKT activation and bax translocation.前列腺素E2通过一种涉及AKT激活和bax易位的机制减少辐射诱导的上皮细胞凋亡。
J Clin Invest. 2004 Dec;114(11):1676-85. doi: 10.1172/JCI22218.
9
The epidermal growth factor-like growth factor amphiregulin is strongly induced by the adenosine 3',5'-monophosphate pathway in various cell types.表皮生长因子样生长因子双调蛋白在多种细胞类型中被3',5'-单磷酸腺苷途径强烈诱导。
Endocrinology. 2004 Nov;145(11):5177-84. doi: 10.1210/en.2004-0232. Epub 2004 Jul 29.
10
Prostaglandin E2 synergistically enhances receptor tyrosine kinase-dependent signaling system in colon cancer cells.前列腺素E2协同增强结肠癌细胞中受体酪氨酸激酶依赖性信号系统。
J Biol Chem. 2004 Apr 2;279(14):14287-93. doi: 10.1074/jbc.M313276200. Epub 2004 Jan 23.

Amphiregulin 促进肠道上皮再生:肠道黏膜下肌成纤维细胞的作用。

Amphiregulin promotes intestinal epithelial regeneration: roles of intestinal subepithelial myofibroblasts.

机构信息

Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.

出版信息

Endocrinology. 2010 Aug;151(8):3728-37. doi: 10.1210/en.2010-0319. Epub 2010 Jun 9.

DOI:10.1210/en.2010-0319
PMID:20534719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2940516/
Abstract

Epidermal growth factor family plays critical roles in intestinal epithelial proliferation and differentiation. The precise function of amphiregulin (AREG), a member of the epidermal growth factor family, in intestinal biology is largely unknown. The present study attempted to address the functional roles of AREG in intestinal epithelial regeneration. Total body irradiation was performed, and intestinal regeneration was assessed in AREG knockout mice. Genetically disruption of AREG significantly impaired intestinal regeneration after radiation injury. It is known that prostaglandin E(2) (PGE(2)) exerts radio-protective and growth-stimulatory effects on intestinal epithelium. We found that PGE(2) radio-protective action did not involve AREG. However, PGE(2) growth-stimulatory effects required functional AREG. Localization of AREG expression was determined by immunohistochemistry in regenerative intestine. The immunoreactivity of AREG was predominantly localized in intestinal subepithelial myofibroblasts (ISEMF). Primary ISEMF cultures were established, and growth-stimulatory actions of ISEMF-generated AREG were demonstrated in cell coculture system. In addition, we found that the cAMP/protein kinase A pathway robustly induced AREG in cultured ISEMF. These studies suggest that AREG plays critical roles in intestinal epithelial growth. Modulation of levels of AREG by targeting ISEMF represents a novel strategy for treatment of certain intestinal disorders.

摘要

表皮生长因子家族在肠道上皮细胞增殖和分化中发挥着关键作用。表皮生长因子家族成员 Amphiregulin(AREG)在肠道生物学中的精确功能在很大程度上尚不清楚。本研究试图探讨 AREG 在肠道上皮细胞再生中的功能作用。进行全身辐射,评估 AREG 敲除小鼠的肠道再生情况。AREG 基因缺失显著损害了辐射损伤后的肠道再生。已知前列腺素 E2(PGE2)对肠道上皮具有放射保护和生长刺激作用。我们发现 PGE2 的放射保护作用不涉及 AREG。然而,PGE2 的生长刺激作用需要功能性 AREG。通过免疫组织化学在再生肠道中确定 AREG 的表达定位。AREG 的免疫反应主要定位于肠道黏膜下肌成纤维细胞(ISEMF)中。建立了原代 ISEMF 培养物,并在细胞共培养系统中证明了 ISEMF 产生的 AREG 的生长刺激作用。此外,我们发现 cAMP/蛋白激酶 A 通路在培养的 ISEMF 中强烈诱导 AREG 的表达。这些研究表明,AREG 在肠道上皮细胞生长中发挥着关键作用。通过靶向 ISEMF 调节 AREG 的水平可能代表治疗某些肠道疾病的一种新策略。