Paehler Vor der Nolte Anja, Chodisetti Giriprakash, Yuan Zhenglin, Busch Florian, Riederer Brigitte, Luo Min, Yu Yan, Menon Manoj B, Schneider Andreas, Stripecke Renata, Nikolovska Katerina, Yeruva Sunil, Seidler Ursula
Departments of Gastroenterology, Hemostatsis, Oncology and Stem Cell Transplantation, Medical School of Hannover, Germany.
Departments of Biochemistry, Hemostatsis, Oncology and Stem Cell Transplantation, Medical School of Hannover, Germany.
J Cell Physiol. 2017 Jul;232(7):1669-1680. doi: 10.1002/jcp.25758. Epub 2017 Feb 21.
Following superficial injury, neighbouring gastric epithelial cells close the wound by rapid cell migration, a process called epithelial restitution. Na /H exchange (NHE) inhibitors interfere with restitution, but the role of the different NHE isoforms expressed in gastric pit cells has remained elusive. The role of the basolaterally expressed NHE1 (Slc9a1) and the presumably apically expressed NHE2 (Slc9a2) in epithelial restitution was investigated in the nontransformed rat gastric surface cell line RGM1. Migration velocity was assessed by loading the cells with the fluorescent dye DiR and following closure of an experimental wound over time. Since RGM1 cells expressed very low NHE2 mRNA and have low transport activity, NHE2 was introduced by lentiviral gene transfer. In medium with pH 7.4, RGM1 cells displayed slow wound healing even in the absence of growth factors and independently of NHE activity. Growth factors accelerated wound healing in a partly NHE1-dependent fashion. Preincubation with acidic pH 7.1 stimulated restitution in a NHE1-dependent fashion. When pH 7.1 was maintained during the restitution period, migratory speed was reduced to ∼10% of the speed at pH 7,4, and the residual restitution was further inhibited by NHE1 inhibition. Lentiviral NHE2 expression increased the steady-state pH and reduced the restitution velocity after low pH preincubation, which was reversible by pharmacological NHE2 inhibition. The results demonstrate that in RGM1 cells, migratory velocity is increased by NHE1 activation, while NHE2 activity inhibit this process. A differential activation of NHE1 and NHE2 may therefore, play a role in the initiation and completion of the epithelial restitution process.
在浅表损伤后,邻近的胃上皮细胞通过快速细胞迁移来闭合伤口,这一过程称为上皮修复。钠/氢交换(NHE)抑制剂会干扰修复过程,但胃小凹细胞中表达的不同NHE亚型的作用仍不清楚。在未转化的大鼠胃表面细胞系RGM1中研究了基底外侧表达的NHE1(Slc9a1)和可能顶端表达的NHE2(Slc9a2)在上皮修复中的作用。通过用荧光染料DiR加载细胞并随时间观察实验伤口的闭合情况来评估迁移速度。由于RGM1细胞表达的NHE2 mRNA非常低且转运活性也低,因此通过慢病毒基因转移引入NHE2。在pH 7.4的培养基中,即使在没有生长因子且与NHE活性无关的情况下,RGM1细胞的伤口愈合也很缓慢。生长因子以部分依赖NHE1的方式加速伤口愈合。用酸性pH 7.1预孵育以依赖NHE1的方式刺激修复。当在修复期间维持pH 7.1时,迁移速度降低至pH 7.4时速度的约10%,并且NHE1抑制进一步抑制了残余的修复。慢病毒NHE2表达增加了稳态pH,并降低了低pH预孵育后的修复速度,这可通过药理学NHE2抑制来逆转。结果表明,在RGM1细胞中,NHE1激活可增加迁移速度,而NHE2活性则抑制这一过程。因此,NHE1和NHE2的差异激活可能在上皮修复过程的启动和完成中起作用。