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Increased core body temperature exacerbates defective protein prenylation in mouse models of mevalonate kinase deficiency

Title: Increased core body temperature exacerbates defective protein prenylation in mouse models of mevalonate kinase deficiency
Authors: Munoz, MA; Skinner, OP; Masle-Farquhar, E; Jurczyluk, J; Xiao, Y; Fletcher, EK; Kristianto, E; Hodson, MP; O’Donoghue, SI; Kaur, S; Brink, R; Zahra, DG; Deenick, EK; Perry, KA; Robertson, AAB; Mehr, S; Hissaria, P; Mulders-Manders, CM; Simon, A; Rogers, MJ
Publisher Information: AMER SOC CLINICAL INVESTIGATION INC
Publication Year: 2022
Collection: The University of Melbourne: Digital Repository
Description: Mevalonate kinase deficiency (MKD) is characterized by recurrent fevers and flares of systemic inflammation, caused by biallelic loss-of-function mutations in MVK. The underlying disease mechanisms and triggers of inflammatory flares are poorly understood because of the lack of in vivo models. We describe genetically modified mice bearing the hypomorphic mutation p.Val377Ile (the commonest variant in patients with MKD) and amorphic, frameshift mutations in Mvk. Compound heterozygous mice recapitulated the characteristic biochemical phenotype of MKD, with increased plasma mevalonic acid and clear buildup of unprenylated GTPases in PBMCs, splenocytes, and bone marrow. The inflammatory response to LPS was enhanced in compound heterozygous mice and treatment with the NLRP3 inflammasome inhibitor MCC950 prevented the elevation of circulating IL-1β, thus identifying a potential inflammasome target for future therapeutic approaches. Furthermore, lines of mice with a range of deficiencies in mevalonate kinase and abnormal prenylation mirrored the genotype-phenotype relationship in human MKD. Importantly, these mice allowed the determination of a threshold level of residual enzyme activity, below which protein prenylation is impaired. Elevated temperature dramatically but reversibly exacerbated the deficit in the mevalonate pathway and the defective prenylation in vitro and in vivo, highlighting increased body temperature as a likely trigger of inflammatory flares.
Document Type: article in journal/newspaper
Language: English
ISSN: 0021-9738
Relation: pii: 160929; https://hdl.handle.net/11343/335083
Availability: https://hdl.handle.net/11343/335083
Rights: https://creativecommons.org/licenses/by/4.0 ; CC BY
Accession Number: edsbas.849285BC
Database: BASE