Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Medicine, Division of Gastroenterology and Hepatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Neurogastroenterol Motil. 2018 Apr;30(4):e13230. doi: 10.1111/nmo.13230. Epub 2017 Oct 20.
The molecular changes that occur in the stomach that are associated with idiopathic gastroparesis are poorly described. The aim of this study was to use quantitative analysis of mRNA expression to identify changes in mRNAs encoding proteins required for the normal motility functions of the stomach.
Full-thickness stomach biopsy samples were collected from non-diabetic control subjects who exhibited no symptoms of gastroparesis and from patients with idiopathic gastroparesis. mRNA was isolated from the muscularis externa and mRNA expression levels were determined by quantitative reverse transcriptase (RT)-PCR.
Smooth muscle tissue from idiopathic gastroparesis patients had decreased expression of mRNAs encoding several contractile proteins, such as MYH11 and MYLK1. Conversely, there was no significant change in mRNAs characteristic of interstitial cells of Cajal (ICCs) such as KIT or ANO1. There was also a significant decrease in mRNA-encoding platelet-derived growth factor receptor α (PDGFRα) and its ligand PDGFB and in Heme oxygenase 1 in idiopathic gastroparesis subjects. In contrast, there was a small increase in mRNA characteristic of neurons. Although there was not an overall change in KIT expression in gastroparesis patients, KIT expression showed a significant correlation with gastric emptying whereas changes in MYLK1, ANO1 and PDGFRα showed weak correlations to the fullness/satiety subscore of patient assessment of upper gastrointestinal disorder-symptom severity index scores.
Our findings suggest that idiopathic gastroparesis is associated with altered smooth muscle cell contractile protein expression and loss of PDGFRα cells without a significant change in ICCs.
与特发性胃轻瘫相关的胃内分子变化描述甚少。本研究旨在采用 mRNA 表达定量分析鉴定编码与胃正常运动功能相关蛋白的 mRNA 变化。
从无糖尿病且无胃轻瘫症状的对照受试者和特发性胃轻瘫患者中采集全层胃活检样本。从外膜分离 mRNA,并通过定量逆转录(RT)-PCR 测定 mRNA 表达水平。
特发性胃轻瘫患者的平滑肌组织中几种收缩蛋白(如 MYH11 和 MYLK1)的编码 mRNA 表达减少。相反,Cajal 间质细胞(ICC)特征性的 mRNAs(如 KIT 或 ANO1)没有明显变化。编码血小板衍生生长因子受体 α(PDGFRα)及其配体 PDGFB 和血红素加氧酶 1 的 mRNA 也显著减少。相反,神经元特征性的 mRNA 略有增加。尽管胃轻瘫患者的 KIT 表达没有总体变化,但 KIT 表达与胃排空呈显著相关,而 MYLK1、ANO1 和 PDGFRα 的变化与患者对上消化道紊乱症状严重指数评分的饱腹感/饱足分项评分呈弱相关。
我们的发现表明,特发性胃轻瘫与平滑肌细胞收缩蛋白表达改变和 PDGFRα 细胞丢失有关,而 ICC 无明显变化。