Mo C, Zhong Y, Wang Y, Yan Z, Li J
Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu 610065, PR China.
Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu 610065, PR China.
Domest Anim Endocrinol. 2014 Jul;48:1-6. doi: 10.1016/j.domaniend.2014.01.002. Epub 2014 Jan 18.
This study characterized the glucagon-like peptide 2 receptor (GLP2R) gene of chickens because relatively little is known about the underlying mechanism of GLP2 actions in nonmammalian species. With the use of reverse transcription PCR, we first cloned the chicken GLP2R (cGLP2R) from adult intestine, which was predicted to encode a 529-amino acid receptor precursor. With the use of a pGL3-CRE luciferase reporter system, we demonstrated that cGLP2R expressed in Chinese hamster ovary cells could be potently activated by cGLP2 (half maximal effective concentration, 1.06 nM) but not by its structurally related peptides, including the newly identified glucagon-like peptide, indicating that cGLP2R is a functional receptor specific to cGLP2. Reverse transcription PCR assay revealed that cGLP2R mRNA was widely expressed in adult chicken tissues, including pancreas and various parts of the gastrointestinal tract. With the use of quantitative real-time reverse transcription PCR assays, we further investigated the mRNA expression of cGLP2R and its potential downstream mediators, epidermal growth factor receptor (EGFR) ligands (heparin-binding EGF-like growth factor, epiregulin, and amphiregulin), in the distal duodenum of developing embryos. The mRNA expression levels of GLP2R and EGFR ligands (heparin-binding EGF-like growth factor and amphiregulin) were shown to increase (P < 0.05 or 0.01) during the late embryonic stages (E16 and E20), implying a potential coordinated action of GLP2 and EGFR ligands on embryonic intestine development. Taken together, our findings not only establish a molecular basis to explore the physiological roles of GLP2 in birds, but they also provide comparative insights into the roles of GLP2R and its ligand in vertebrates, such as its roles in embryonic intestine development.
本研究对鸡的胰高血糖素样肽2受体(GLP2R)基因进行了特征分析,因为对于非哺乳动物物种中GLP2作用的潜在机制了解相对较少。通过逆转录PCR,我们首先从成年鸡肠道中克隆了鸡GLP2R(cGLP2R),预计其编码一个529个氨基酸的受体前体。使用pGL3-CRE荧光素酶报告系统,我们证明在中国仓鼠卵巢细胞中表达的cGLP2R可被cGLP2有效激活(半数最大效应浓度,1.06 nM),但不能被其结构相关肽激活,包括新鉴定的胰高血糖素样肽,这表明cGLP2R是cGLP2特异性的功能性受体。逆转录PCR分析显示,cGLP2R mRNA在成年鸡组织中广泛表达,包括胰腺和胃肠道的各个部位。通过使用定量实时逆转录PCR分析,我们进一步研究了发育中胚胎十二指肠远端cGLP2R及其潜在下游介质表皮生长因子受体(EGFR)配体(肝素结合表皮生长因子样生长因子、上皮调节素和双调蛋白)的mRNA表达。在胚胎后期阶段(E16和E20),GLP2R和EGFR配体(肝素结合表皮生长因子样生长因子和双调蛋白)的mRNA表达水平显示升高(P < 0.05或0.01),这意味着GLP2和EGFR配体在胚胎肠道发育中可能存在协同作用。综上所述,我们的研究结果不仅为探索GLP2在鸟类中的生理作用建立了分子基础,还为GLP2R及其配体在脊椎动物中的作用提供了比较性见解,例如它们在胚胎肠道发育中的作用。