Department of Pediatrics, National Jewish Health, Denver, Colorado, USA.
Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
BMJ Open Respir Res. 2021 Feb;8(1). doi: 10.1136/bmjresp-2020-000861.
The incubation of airway epithelia cells at low temperatures is a common in vitro experimental approach used in the field of cystic fibrosis (CF) research to thermo-stabilise F508del-CFTR and increase its functional expression. Given that the airway epithelium includes numerous ion transporters other than CFTR, we hypothesised that there was an impact of low temperature incubation on CFTR-independent ionoregulatory mechanisms in airway epithelia derived from individuals with and without CF.
After differentiation at the air-liquid interface, nasal epithelia were incubated at either 37°C or 29°C (low temperature) for 48 hours prior to analysis in an Ussing chamber.
While F508del-CFTR activity was increased after low temperature incubation, activity of CFTR in non-CF epithelia was unchanged. Importantly, cultures incubated at 29°C demonstrated decreased transepithelial potential difference (TEPD) and short-circuit currents (Isc) at baseline. The predominant factor contributing to the reduced baseline TEPD and Isc in 29°C cultures was the reduced activity of the epithelial sodium channel (ENaC), evidenced by a reduced responsiveness to amiloride. This effect was observed in cells derived from both non-CF and CF donors.
Significant transcriptional downregulation of ENaC subunits β and γ were observed, which may partially explain the decreased ENaC activity. We speculate that low temperature incubation may be a useful experimental paradigm to reduce ENaC activity in in vitro epithelial cultures.
在囊性纤维化(CF)研究领域,低温孵育气道上皮细胞是一种常用的体外实验方法,可使 F508del-CFTR 热稳定并增加其功能表达。由于气道上皮细胞除 CFTR 外还包含许多离子转运体,我们假设低温孵育对 CF 和非 CF 个体来源的气道上皮中 CFTR 非依赖性离子调节机制有影响。
在气液界面分化后,将鼻上皮细胞在 37°C 或 29°C(低温)下孵育 48 小时,然后在 Ussing 室中进行分析。
虽然低温孵育后 F508del-CFTR 的活性增加,但非 CF 上皮细胞中 CFTR 的活性不变。重要的是,在 29°C 孵育的培养物中,基础 TEPD 和短路电流(Isc)降低。在 29°C 培养物中,降低基础 TEPD 和 Isc 的主要因素是上皮钠通道(ENaC)的活性降低,这可以通过对阿米洛利的反应性降低来证明。这种效应在非 CF 和 CF 供体来源的细胞中均观察到。
观察到 ENaC 亚基 β 和 γ 的显著转录下调,这可能部分解释了 ENaC 活性的降低。我们推测,低温孵育可能是一种有用的实验范例,可以降低体外上皮培养物中的 ENaC 活性。