Boj Sylvia F, Vonk Annelotte M, Statia Marvin, Su Jinyi, Vries Robert R G, Beekman Jeffrey M, Clevers Hans
Foundation Hubrecht Organoid Technology.
Department of Pediatric Pulmonology, Regenerative Medicine Centre Utrecht, Wilhelmina Children's Hospital, University Medical Centre Utrecht.
J Vis Exp. 2017 Feb 11(120):55159. doi: 10.3791/55159.
Recently-developed cystic fibrosis transmembrane conductance regulator (CFTR)-modulating drugs correct surface expression and/or function of the mutant CFTR channel in subjects with cystic fibrosis (CF). Identification of subjects that may benefit from these drugs is challenging because of the extensive heterogeneity of CFTR mutations, as well as other unknown factors that contribute to individual drug efficacy. Here, we describe a simple and relatively rapid assay for measuring individual CFTR function and response to CFTR modulators in vitro. Three dimensional (3D) epithelial organoids are grown from rectal biopsies in standard organoid medium. Once established, the organoids can be bio-banked for future analysis. For the assay, 30-80 organoids are seeded in 96-well plates in basement membrane matrix and are then exposed to drugs. One day later, the organoids are stained with calcein green, and forskolin-induced swelling is monitored by confocal live cell microscopy at 37 °C. Forskolin-induced swelling is fully CFTR-dependent and is sufficiently sensitive and precise to allow for discrimination between the drug responses of individuals with different and even identical CFTR mutations. In vitro swell responses correlate with the clinical response to therapy. This assay provides a cost-effective approach for the identification of drug-responsive individuals, independent of their CFTR mutations. It may also be instrumental in the development of future CFTR modulators.
最近研发的囊性纤维化跨膜传导调节因子(CFTR)调节剂可纠正囊性纤维化(CF)患者体内突变CFTR通道的表面表达和/或功能。由于CFTR突变具有广泛的异质性,以及其他影响个体药物疗效的未知因素,确定可能从这些药物中获益的患者具有挑战性。在此,我们描述了一种简单且相对快速的体外测定方法,用于测量个体CFTR功能以及对CFTR调节剂的反应。三维(3D)上皮类器官由直肠活检组织在标准类器官培养基中培养而成。一旦建立,这些类器官可进行生物储存以供未来分析。在该测定中,将30 - 80个类器官接种于96孔板中的基底膜基质中,然后使其接触药物。一天后,用钙黄绿素对类器官进行染色,并在37℃下通过共聚焦活细胞显微镜监测福司可林诱导的肿胀情况。福司可林诱导的肿胀完全依赖于CFTR,并且足够灵敏和精确,能够区分具有不同甚至相同CFTR突变个体的药物反应。体外肿胀反应与临床治疗反应相关。该测定为识别药物反应个体提供了一种经济有效的方法,且与他们的CFTR突变无关。它也可能有助于未来CFTR调节剂的研发。