GENYO, Centre for Genomics and Oncological Research: Pfizer, University of Granada, Andalusian Regional Government PTS Granada-Avenida de la Ilustración 114, 18016 Granada, Spain.
Department of Medicinal & Organic Chemistry and Excellence Research Unit of "Chemistry Applied to Biomedicine and the Environment", Faculty of Pharmacy, University of Granada, Campus de Cartuja s/n, 18071 Granada, Spain.
Int J Mol Sci. 2022 Jun 4;23(11):6298. doi: 10.3390/ijms23116298.
Pompe disease (PD) is a rare disorder caused by mutations in the acid alpha-glucosidase (GAA) gene. Most gene therapies (GT) partially rely on the cross-correction of unmodified cells through the uptake of the GAA enzyme secreted by corrected cells. In the present study, we generated isogenic murine GAA-KO cell lines resembling severe mutations from Pompe patients. All of the generated GAA-KO cells lacked GAA activity and presented an increased autophagy and increased glycogen content by means of myotube differentiation as well as the downregulation of mannose 6-phosphate receptors (CI-MPRs), validating them as models for PD. Additionally, different chimeric murine GAA proteins (IFG, IFLG and 2G) were designed with the aim to improve their therapeutic activity. Phenotypic rescue analyses using lentiviral vectors point to IFG chimera as the best candidate in restoring GAA activity, normalising the autophagic marker p62 and surface levels of CI-MPRs. Interestingly, in vivo administration of liver-directed AAVs expressing the chimeras further confirmed the good behaviour of IFG, achieving cross-correction in heart tissue. In summary, we generated different isogenic murine muscle cell lines mimicking the severe PD phenotype, as well as validating their applicability as preclinical models in order to reduce animal experimentation.
庞贝病(PD)是一种由酸性α-葡萄糖苷酶(GAA)基因突变引起的罕见疾病。大多数基因治疗(GT)部分依赖于未修饰细胞通过摄取经校正细胞分泌的 GAA 酶进行交叉校正。在本研究中,我们生成了类似于庞贝病患者严重突变的同基因小鼠 GAA-KO 细胞系。所有生成的 GAA-KO 细胞均缺乏 GAA 活性,并通过肌管分化表现出自噬增加和糖原含量增加,以及甘露糖 6-磷酸受体(CI-MPRs)下调,验证了它们作为 PD 模型的适用性。此外,设计了不同的嵌合小鼠 GAA 蛋白(IFG、IFLG 和 2G),旨在提高其治疗活性。使用慢病毒载体进行的表型挽救分析表明,IFG 嵌合体是恢复 GAA 活性、使自噬标志物 p62 和 CI-MPRs 表面水平正常化的最佳候选物。有趣的是,表达嵌合体的肝靶向 AAVs 的体内给药进一步证实了 IFG 的良好行为,在心脏组织中实现了交叉校正。总之,我们生成了不同的同基因小鼠肌肉细胞系,模拟了严重 PD 表型,并验证了它们作为临床前模型的适用性,以减少动物实验。