Shaanxi Key Laboratory for Animal Conservation, Northwest University, Xi'an 710069, China.
Key Laboratory of Resource Biology and Biotechnology in Western China (College of Life Sciences, Northwest University), Ministry of Education, 229# North Taibai Road, Xi'an 710069, China.
Int J Mol Sci. 2022 Aug 12;23(16):9026. doi: 10.3390/ijms23169026.
Both pathological conditions and hibernation can affect the barrier function of small intestine mucosa. However, the effect of hibernation on the barrier function of colonic mucosa remains unclear.
We investigated morphological changes in colonic mucosa, the concentrations of specific proteins and molecules, and the enzymatic activity of diamine oxidase (DAO), in serum and colonic tissue; the expression of tight junction proteins and mucin, and the changes in inflammatory, farnesoid X receptor (FXR)-small heterodimer partner (SHP), and apoptosis-related molecules that could play a role in gut permeability changes in Daurian ground squirrels in summer active (SA), late torpor (LT), and interbout arousal (IBA) periods.
The results show that hibernation reduced the thickness of the colonic mucosa and the depth of the crypt, decreased the number of goblet cells (GCs), and damaged the structure of some microvilli. The concentrations of proteins and molecules, and the enzymatic activity of DAO, were all increased in the serum and colon, and the localization of tight junction proteins and mucin in the colonic mucosa were altered (compensatory response). Although the ground squirrels ate during the interbout arousal period, the changes remained similar to the response to torpor. Inflammation, apoptosis-anti-apoptosis, and FXR-SHP signaling may be involved in the possible changes in intestinal gut permeability during the torpor-arousal cycle in Daurian ground squirrels. In addition, periodic interbout arousal may play an inflammation-correcting role during the long hibernation season of Daurian ground squirrels.
病理状态和冬眠都会影响小肠黏膜的屏障功能。然而,冬眠对结肠黏膜屏障功能的影响尚不清楚。
我们研究了达乌尔黄鼠在夏季活跃(SA)、晚期蛰伏(LT)和觉醒间歇(IBA)期间结肠黏膜的形态变化,血清和结肠组织中特定蛋白质和分子的浓度,二胺氧化酶(DAO)的酶活性;紧密连接蛋白和粘蛋白的表达;以及可能在肠道通透性变化中起作用的炎症、法尼醇 X 受体(FXR)-小异二聚体伴侣(SHP)和凋亡相关分子的变化。
结果表明,冬眠会降低结肠黏膜的厚度和隐窝的深度,减少杯状细胞(GCs)的数量,并损伤一些微绒毛的结构。血清和结肠中蛋白质和分子的浓度以及 DAO 的酶活性均升高,结肠黏膜中紧密连接蛋白和粘蛋白的定位发生改变(代偿反应)。尽管达乌尔黄鼠在觉醒间歇期进食,但这些变化仍类似于对蛰伏的反应。炎症、凋亡-抗凋亡和 FXR-SHP 信号转导可能参与了达乌尔黄鼠蛰伏-觉醒周期中肠道通透性的变化。此外,周期性的觉醒间歇可能在达乌尔黄鼠漫长的冬眠季节中发挥炎症纠正作用。