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Ablation of microRNA-155 and neuroinflammation in a mouse model of CLN1-disease.
Sadhukhan, Tamal; Bagh, Maria B; Sadhukhan, Sriparna; Appu, Abhilash P; Mondal, Avisek; Iiben, James R; Li, Tianwei; Coon, Steven L; Mukherjee, Anil B.
Afiliação
  • Sadhukhan T; Section on Developmental Genetics, Division on Translational Medicine, USA. Electronic address: tamal.sadhukhan@nih.gov.
  • Bagh MB; Section on Developmental Genetics, Division on Translational Medicine, USA.
  • Sadhukhan S; Section on Developmental Genetics, Division on Translational Medicine, USA.
  • Appu AP; Section on Developmental Genetics, Division on Translational Medicine, USA.
  • Mondal A; Section on Developmental Genetics, Division on Translational Medicine, USA.
  • Iiben JR; Molecular Genomics Core (HNT417), Eunice Kennedy Shriver National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, MD, 20892-1830, USA.
  • Li T; Molecular Genomics Core (HNT417), Eunice Kennedy Shriver National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, MD, 20892-1830, USA.
  • Coon SL; Molecular Genomics Core (HNT417), Eunice Kennedy Shriver National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, MD, 20892-1830, USA.
  • Mukherjee AB; Section on Developmental Genetics, Division on Translational Medicine, USA. Electronic address: mukherja@exchange.nih.gov.
Biochem Biophys Res Commun ; 571: 137-144, 2021 09 24.
Article em En | MEDLINE | ID: mdl-34325129
Infantile neuronal ceroid lipofuscinosis (INCL), also known as CLN1-disease, is a devastating neurodegenerative lysosomal storage disorder (LSD), caused by inactivating mutations in the CLN1 gene. The Cln1-/- mice, which mimic INCL, manifest progressive neuroinflammation contributing to neurodegeneration. However, the underlying mechanism of neuroinflammation in INCL and in Cln1-/- mice has remained elusive. Previously, it has been reported that microRNA-155 (miR-155) regulates inflammation and miR profiling in Cln1-/- mouse brain showed that the level of miR-155 was upregulated. Thus, we sought to determine whether ablation of miR-155 in Cln1-/- mice may suppress neuroinflammation in these mice. Towards this goal, we generated Cln1-/-/miR-155-/- double-knockout mice and evaluated the inflammatory signatures in the brain. We found that the brains of double-KO mice manifest progressive neuroinflammatory changes virtually identical to those found in Cln1-/- mice. We conclude that ablation of miR-155 in Cln1-/- mice does not alter the neuroinflammatory trajectory in INCL mouse model.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tioléster Hidrolases / MicroRNAs / Modelos Animais de Doenças / Inflamação Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tioléster Hidrolases / MicroRNAs / Modelos Animais de Doenças / Inflamação Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article