Rymut Sharon M, Ivy Tracy, Corey Deborah A, Cotton Calvin U, Burgess James D, Kelley Thomas J
Departments of 1 Pharmacology.
2 Pediatrics, and.
Am J Respir Cell Mol Biol. 2015 Dec;53(6):853-62. doi: 10.1165/rcmb.2014-0462OC.
The regulation of microtubule dynamics in cystic fibrosis (CF) epithelial cells and the consequences of reduced rates of microtubule polymerization on downstream CF cellular events, such as cholesterol accumulation, a marker of impaired intracellular transport, are explored here. It is identified that microtubules in both CF cell models and in primary CF nasal epithelial cells repolymerize at a slower rate compared with respective controls. Previous studies suggest a role for cAMP in modulating organelle transport in CF cells, implicating a role for exchange protein activated by cAMP (EPAC) 1, a regulator of microtubule elongation, as a potential mechanism. EPAC1 activity is reduced in CF cell models and in Cftr(-/-) mouse lung compared with respective non-CF controls. Stimulation of EPAC1 activity with the selective EPAC1 agonist, 8-cpt-2-O-Me-cAMP, stimulates microtubule repolymerization to wild-type rates in CF cells. EPAC1 activation also alleviates cholesterol accumulation in CF cells, suggesting a direct link between microtubule regulation and intracellular transport. To verify the relationship between transport and microtubule regulation, expression of the protein, tubulin polymerization-promoting protein, was knocked down in non-CF human tracheal (9/HTEo(-)) cells to mimic the microtubule dysregulation in CF cells. Transduced cells with short hairpin RNA targeting tubulin polymerization-promoting protein exhibit CF-like perinuclear cholesterol accumulation and other cellular manifestations of CF cells, thus supporting a role for microtubule regulation as a mechanism linking CFTR function to downstream cellular manifestation.
本文探讨了囊性纤维化(CF)上皮细胞中微管动力学的调节,以及微管聚合速率降低对下游CF细胞事件(如胆固醇积累,这是细胞内运输受损的一个标志)的影响。研究发现,与各自的对照相比,CF细胞模型和原发性CF鼻上皮细胞中的微管重新聚合的速率较慢。先前的研究表明,cAMP在调节CF细胞中的细胞器运输中起作用,这暗示了由cAMP激活的交换蛋白(EPAC)1(一种微管伸长调节剂)作为一种潜在机制发挥作用。与各自的非CF对照相比,CF细胞模型和Cftr(-/-)小鼠肺中的EPAC1活性降低。用选择性EPAC1激动剂8-cpt-2-O-Me-cAMP刺激EPAC1活性,可刺激CF细胞中的微管重新聚合至野生型速率。EPAC1激活还可减轻CF细胞中的胆固醇积累,这表明微管调节与细胞内运输之间存在直接联系。为了验证运输与微管调节之间的关系,在非CF人气管(9/HTEo(-))细胞中敲低微管蛋白聚合促进蛋白的表达,以模拟CF细胞中的微管失调。用靶向微管蛋白聚合促进蛋白的短发夹RNA转导的细胞表现出CF样的核周胆固醇积累和CF细胞的其他细胞表现,从而支持微管调节作为将CFTR功能与下游细胞表现联系起来的一种机制的作用。