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阿片肽及其受体在啮齿动物胃肠道中的个体发生。

Ontogeny of apelin and its receptor in the rodent gastrointestinal tract.

作者信息

Wang Guiyun, Kundu Ramendra, Han Song, Qi Xiang, Englander Ella W, Quertermous Thomas, Greeley George H

机构信息

Department of Surgery, University of Texas Medical Branch, 301 University Boulevard, Galveston, Texas 77555, USA.

出版信息

Regul Pept. 2009 Nov 27;158(1-3):32-9. doi: 10.1016/j.regpep.2009.07.016. Epub 2009 Aug 4.

Abstract

Apelin is the endogenous ligand for the APJ receptor and both apelin and APJ are expressed in the gastrointestinal (GI) tract. The aim of this study was to define ontogeny of apelin and APJ in the developing rodent GI tract by measuring expression levels and characterizing abundance and cellular localization at an embryonic stage (E18.5 or E21), two postnatal stages (P4, P16) and in the adult. Apelin and APJ mRNA levels were measured by real time RT-PCR, apelin and APJ-containing cells were identified by immunohistochemical (IHC) staining. Gastric, duodenal and colonic apelin and APJ mRNA levels were highest at birth and declined postnatally. In the postnatal rat stomach, few apelin peptide-containing cells were identified, the density of gastric apelin-containing cells increased progressively after weaning and into adulthood. A robust APJ immunostaining was observed postnatally in the epithelium, intestinal goblet cells and in smooth muscle cells. In the adult rat, APJ immunostaining in the surface epithelium and goblet cells decreased markedly. During the early postnatal period, in an apelin-deficient mouse, APJ expression and immunostaining in the gut were reduced suggesting that apelin regulates APJ. Together, our data support a role for the apelin-APJ system in the regulation of smooth muscle, epithelial and goblet cell function in the GI tract.

摘要

阿片肽是APJ受体的内源性配体,阿片肽和APJ均在胃肠道(GI)中表达。本研究的目的是通过测量胚胎期(E18.5或E21)、两个出生后阶段(P4、P16)以及成年期的表达水平,并表征丰度和细胞定位,来确定阿片肽和APJ在发育中的啮齿动物胃肠道中的个体发生情况。通过实时RT-PCR测量阿片肽和APJ的mRNA水平,通过免疫组织化学(IHC)染色鉴定含阿片肽和APJ的细胞。胃、十二指肠和结肠的阿片肽和APJ mRNA水平在出生时最高,出生后下降。在出生后的大鼠胃中,很少能鉴定出含阿片肽的细胞,断奶后直至成年,胃中含阿片肽细胞的密度逐渐增加。出生后在上皮细胞、肠杯状细胞和平滑肌细胞中观察到强烈的APJ免疫染色。在成年大鼠中,表面上皮和杯状细胞中的APJ免疫染色明显减少。在出生后早期,在阿片肽缺陷小鼠中,肠道中的APJ表达和免疫染色减少,这表明阿片肽调节APJ。总之,我们的数据支持阿片肽-APJ系统在调节胃肠道平滑肌、上皮和杯状细胞功能中的作用。

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