Bonser Luke R, Schroeder Bradley W, Ostrin Lisa A, Baumlin Nathalie, Olson Jean L, Salathe Matthias, Erle David J
1 Lung Biology Center and.
2 College of Optometry, University of Houston, Houston, Texas; and.
Am J Respir Cell Mol Biol. 2015 Oct;53(4):536-43. doi: 10.1165/rcmb.2014-0318OC.
Protein disulfide isomerase (PDI) family members regulate protein folding and calcium homeostasis in the endoplasmic reticulum (ER). The PDI family member anterior gradient (AGR) 3 is expressed in the airway, but the localization, regulation, and function of AGR3 are poorly understood. Here we report that AGR3, unlike its closest homolog AGR2, is restricted to ciliated cells in the airway epithelium and is not induced by ER stress. Mice lacking AGR3 are viable and develop ciliated cells with normal-appearing cilia. However, ciliary beat frequency was lower in airways from AGR3-deficient mice compared with control mice (20% lower in the absence of stimulation and 35% lower after ATP stimulation). AGR3 deficiency had no detectable effects on ciliary beat frequency (CBF) when airways were perfused with a calcium-free solution, suggesting that AGR3 is required for calcium-mediated regulation of ciliary function. Decreased CBF was associated with impaired mucociliary clearance in AGR3-deficient airways. We conclude that AGR3 is a specialized member of the PDI family that plays an unexpected role in the regulation of CBF and mucociliary clearance in the airway.
蛋白质二硫键异构酶(PDI)家族成员在内质网(ER)中调节蛋白质折叠和钙稳态。PDI家族成员前梯度蛋白(AGR)3在气道中表达,但对AGR3的定位、调控和功能了解甚少。在此我们报告,与最接近的同源物AGR2不同,AGR3局限于气道上皮的纤毛细胞,且不受内质网应激诱导。缺乏AGR3的小鼠可存活,其发育出的纤毛细胞具有外观正常的纤毛。然而,与对照小鼠相比,AGR3缺陷小鼠气道中的纤毛摆动频率较低(在无刺激时低20%,在ATP刺激后低35%)。当气道用无钙溶液灌注时,AGR3缺陷对纤毛摆动频率(CBF)没有可检测到的影响,这表明AGR3是钙介导的纤毛功能调节所必需的。CBF降低与AGR3缺陷气道中的黏液纤毛清除受损有关。我们得出结论,AGR3是PDI家族的一个特殊成员,在气道中CBF和黏液纤毛清除的调节中发挥着意想不到的作用。