Literature DB >> 29873499

Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice.

Frida Torell1,2, Kate Bennett3, Silvia Cereghini4,5,6, Mélanie Fabre4,5,6, Stefan Rännar3, Katrin Lundstedt-Enkel3,7, Thomas Moritz3,8, Cécile Haumaitre4,5,6, Johan Trygg1, Torbjörn Lundstedt3,9.   

Abstract

In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development.

Entities:  

Keywords:  HNF1B-associated diseases; MODY5; OPLS-DA; RCAD; metabolomics; mouse model; multiorgan samples

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Year:  2018        PMID: 29873499     DOI: 10.1021/acs.jproteome.7b00821

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  2 in total

1.  Hnf1b haploinsufficiency differentially affects developmental target genes in a new renal cysts and diabetes mouse model.

Authors:  Leticia L Niborski; Mélanie Paces-Fessy; Pierbruno Ricci; Adeline Bourgeois; Pedro Magalhães; Maria Kuzma-Kuzniarska; Celine Lesaulnier; Martin Reczko; Edwige Declercq; Petra Zürbig; Alain Doucet; Muriel Umbhauer; Silvia Cereghini
Journal:  Dis Model Mech       Date:  2021-05-04       Impact factor: 5.758

2.  Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.

Authors:  Beata Małachowska; Justyna Janikiewicz; Karolina Pietrowska; Krystyna Wyka; Joanna Madzio; Kamila Wypyszczak; Marcin Tkaczyk; Sławomir Chrul; Rafał Zwiech; Anna Hogendorf; Maciej T Małecki; Maciej Borowiec; Adam Krętowski; Wojciech Młynarski; Agnieszka Dobrzyń; Michał Ciborowski; Wojciech Fendler
Journal:  Metabolomics       Date:  2022-02-18       Impact factor: 4.290

  2 in total

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