| Literature DB >> 28888852 |
Benjamin L Farah1, Dustin J Landau2, Yajun Wu3, Rohit A Sinha1, Alwin Loh4, Boon-Huat Bay3, Dwight D Koeberl2, Paul M Yen5.
Abstract
GSD Ia (von Gierke Disease, Glycogen Storage Disease Type Ia) is a devastating genetic disorder with long-term sequelae, such as non-alcoholic fatty liver disease and renal failure. Down-regulated autophagy is involved in the development of hepatic metabolic dysfunction in GSD Ia; however, the role of autophagy in the renal pathology is unknown. Here we show that autophagy is impaired and endoplasmic reticulum (ER) stress is increased in the kidneys of a mouse model of GSD Ia. Induction of autophagy by rapamycin also reduces this ER stress. Taken together, these results show an additional role for autophagy down-regulation in the pathogenesis of GSD Ia, and provide further justification for the use of autophagy modulators in GSD Ia.Entities:
Keywords: Autophagy; ER stress; GSD Ia; Glucose-6-phosphatase; Glucose-6-phosphate; Glycogen storage disease type I; Kidney; Rapamycin; Von Gierke's disease
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Year: 2017 PMID: 28888852 PMCID: PMC5722666 DOI: 10.1016/j.ymgme.2017.08.013
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797