{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["17(1)"],"submitter":["Vardi A"],"funding":["Children&apos;s Gaucher Research Fund"],"pubmed_abstract":["<h4>Background</h4>The type 1 interferon (IFN) response is part of the innate immune response and best known for its role in viral and bacterial infection. However, this pathway is also induced in sterile inflammation such as that which occurs in a number of neurodegenerative diseases, including neuronopathic Gaucher disease (nGD), a lysosomal storage disorder (LSD) caused by mutations in GBA.<h4>Methods</h4>Mice were injected with conduritol B-epoxide, an irreversible inhibitor of acid beta-glucosidase, the enzyme defective in nGD. MyTrMaSt null mice, where four adaptors of pathogen recognition receptors (PRRs) are deficient, were used to determine the role of the IFN pathway in nGD pathology. Activation of inflammatory and other pathways was analyzed by a variety of methods including RNA"],"journal":["Journal of neuroinflammation"],"pagination":["265"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7487497"],"repository":["biostudies-literature"],"pubmed_title":["Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease."],"pmcid":["PMC7487497"],"pubmed_authors":["Cho SM","Kalinke U","Spanier J","Ben-Dor S","Futerman AH","Vardi A"],"additional_accession":[]},"is_claimable":false,"name":"Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease.","description":"<h4>Background</h4>The type 1 interferon (IFN) response is part of the innate immune response and best known for its role in viral and bacterial infection. However, this pathway is also induced in sterile inflammation such as that which occurs in a number of neurodegenerative diseases, including neuronopathic Gaucher disease (nGD), a lysosomal storage disorder (LSD) caused by mutations in GBA.<h4>Methods</h4>Mice were injected with conduritol B-epoxide, an irreversible inhibitor of acid beta-glucosidase, the enzyme defective in nGD. MyTrMaSt null mice, where four adaptors of pathogen recognition receptors (PRRs) are deficient, were used to determine the role of the IFN pathway in nGD pathology. Activation of inflammatory and other pathways was analyzed by a variety of methods including RNA","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Sep","modification":"2026-07-15T21:38:21.333Z","creation":"2026-07-09T10:15:34.226Z"},"accession":"S-EPMC7487497","cross_references":{"pubmed":["32892753"],"doi":["10.1186/s12974-020-01934-x"]}}