Literature DB >> 35508755

An explanation for the decreased severity of liver malfunction in Niemann-Pick C1 disease with age.

Robert P Erickson1, Lawrence I Grossman2, Siddhesh Aras2.   

Abstract

Niemann-Pick C disease frequently presents as severe cholestatic disease in infants. However, it progressively becomes less of a problem as children age. We have found that, in an appropriate mouse model, liver cholesterol levels, which are initially very high, decrease while mitochondrial function, initially quite compromised, increases with age. The key mitochondrial regulator, MNRR1, increases in parallel with the increase in mitochondrial function. These changes appear to explain the amelioration of the liver disease that occurs with time in this disorder.
© 2022. The Author(s), under exclusive licence to Institute of Plant Genetics Polish Academy of Sciences.

Entities:  

Keywords:  Cholesterol; Infantile hepatic storage disease; Liver; MNRR1; Nieman Pick C1 disease

Mesh:

Year:  2022        PMID: 35508755     DOI: 10.1007/s13353-022-00695-y

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   2.653


  2 in total

Review 1.  Niemann-Pick disease type C.

Authors:  Marie T Vanier
Journal:  Orphanet J Rare Dis       Date:  2010-06-03       Impact factor: 4.123

2.  Acid ceramidase improves mitochondrial function and oxidative stress in Niemann-Pick type C disease by repressing STARD1 expression and mitochondrial cholesterol accumulation.

Authors:  Sandra Torres; Estel Solsona-Vilarrasa; Susana Nuñez; Nuria Matías; Naroa Insausti-Urkia; Fernanda Castro; Mireia Casasempere; Gemma Fabriás; Josefina Casas; Carlos Enrich; José C Fernández-Checa; Carmen Garcia-Ruiz
Journal:  Redox Biol       Date:  2021-06-19       Impact factor: 11.799

  2 in total

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