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Network analysis identifies strain-dependent response to tau and tau seeding-associated genes.
Acri, Dominic J; You, Yanwen; Tate, Mason D; Karahan, Hande; Martinez, Pablo; McCord, Brianne; Sharify, A Daniel; John, Sutha; Kim, Byungwook; Dabin, Luke C; Philtjens, Stéphanie; Wijeratne, H R Sagara; McCray, Tyler J; Smith, Daniel C; Bissel, Stephanie J; Lamb, Bruce T; Lasagna-Reeves, Cristian A; Kim, Jungsu.
Affiliation
  • Acri DJ; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • You Y; Medical Neuroscience Graduate Program, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Tate MD; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • Karahan H; Department of Anatomy, Cell Biology and Physiology, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Martinez P; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • McCord B; Medical Neuroscience Graduate Program, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Sharify AD; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • John S; Department of Medical and Molecular Genetics, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Kim B; Department of Anatomy, Cell Biology and Physiology, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Dabin LC; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • Philtjens S; Department of Medical and Molecular Genetics, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Wijeratne HRS; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • McCray TJ; Department of Medical and Molecular Genetics, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Smith DC; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • Bissel SJ; Department of Medical and Molecular Genetics, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Lamb BT; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
  • Lasagna-Reeves CA; Department of Medical and Molecular Genetics, Indiana UniversitySchool of Medicine, Indianapolis, IN, USA.
  • Kim J; Stark Neurosciences Research Institute, Indiana University School of Medicine , Indianapolis, IN, USA.
J Exp Med ; 220(11)2023 11 06.
Article in En | MEDLINE | ID: mdl-37606887
ABSTRACT
Previous research demonstrated that genetic heterogeneity is a critical factor in modeling amyloid accumulation and other Alzheimer's disease phenotypes. However, it is unknown what mechanisms underlie these effects of genetic background on modeling tau aggregate-driven pathogenicity. In this study, we induced tau aggregation in wild-derived mice by expressing MAPT. To investigate the effect of genetic background on the action of tau aggregates, we performed RNA sequencing with brains of C57BL/6J, CAST/EiJ, PWK/PhJ, and WSB/EiJ mice (n = 64) and determined core transcriptional signature conserved in all genetic backgrounds and signature unique to wild-derived backgrounds. By measuring tau seeding activity using the cortex, we identified 19 key genes associated with tau seeding and amyloid response. Interestingly, microglial pathways were strongly associated with tau seeding activity in CAST/EiJ and PWK/PhJ backgrounds. Collectively, our study demonstrates that mouse genetic context affects tau-mediated alteration of transcriptome and tau seeding. The gene modules associated with tau seeding provide an important resource to better model tauopathy.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Tauopathies / Alzheimer Disease Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Tauopathies / Alzheimer Disease Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Year: 2023 Type: Article