Yi Haiqing, Zhang Quan, Yang Chunyu, Kishnani Priya S, Sun Baodong
Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC, 27710, USA.
College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, 225009, China.
JIMD Rep. 2016;30:89-94. doi: 10.1007/8904_2015_522. Epub 2016 Jun 26.
Deficiency of glycogen branching enzyme in glycogen storage disease type IV (GSD IV) results in accumulation of less-branched and poorly soluble polysaccharides (polyglucosan bodies) in multiple tissues. Standard enzymatic method, when used to quantify glycogen content in GSD IV tissues, causes significant loss of the polysaccharides during preparation of tissue lysates. We report a modified method including an extra boiling step to dissolve the insoluble glycogen, ultimately preserving the glycogen content in tissue homogenates from GSD IV mice. Muscle tissues from wild-type, GSD II and GSD IV mice and GSD III dogs were homogenized in cold water, and homogenate of each tissue was divided into two parts. One part was immediately clarified by centrifugation at 4°C (STD-prep); the other part was boiled for 5 min then centrifuged (Boil-prep) at room temperature. When glycogen was quantified enzymatically in tissue lysates, no significant differences were found between the STD-prep and the Boil-prep for wild-type, GSD II and GSD III muscles. In contrast, glycogen content for GSD IV muscle in the STD-prep was only 11% of that in the Boil-prep, similar to wild-type values. Similar results were observed in other tissues of GSD IV mice and fibroblast cells from a GSD IV patient. This study provides important information for improving disease diagnosis, monitoring disease progression, and evaluating treatment outcomes in both clinical and preclinical clinical settings for GSD IV. This report should be used as an updated protocol in clinical diagnostic laboratories.
糖原贮积病IV型(GSD IV)中糖原分支酶的缺乏导致多组织中分支较少且溶解性差的多糖(多聚葡萄糖体)积累。当使用标准酶法对GSD IV组织中的糖原含量进行定量时,在制备组织裂解物的过程中会导致大量多糖损失。我们报告了一种改进方法,包括额外的煮沸步骤以溶解不溶性糖原,最终保留GSD IV小鼠组织匀浆中的糖原含量。将野生型、GSD II和GSD IV小鼠以及GSD III犬的肌肉组织在冷水中匀浆,每个组织的匀浆分为两部分。一部分立即在4°C下离心澄清(STD制备);另一部分煮沸5分钟,然后在室温下离心(煮沸制备)。当对组织裂解物中的糖原进行酶定量时,野生型、GSD II和GSD III肌肉的STD制备和煮沸制备之间未发现显著差异。相比之下,STD制备中GSD IV肌肉的糖原含量仅为煮沸制备中的11%,与野生型值相似。在GSD IV小鼠的其他组织和一名GSD IV患者的成纤维细胞中也观察到了类似结果。本研究为改善GSD IV临床和临床前环境中的疾病诊断、监测疾病进展以及评估治疗结果提供了重要信息。本报告应作为临床诊断实验室的更新方案使用。