Brain Aggregates: An Effective In Vitro Cell Culture System Modeling Neurodegenerative Diseases

J Neuropathol Exp Neurol. 2016 Mar;75(3):256-62. doi: 10.1093/jnen/nlv025. Epub 2016 Feb 6.

Abstract

Drug discovery for neurodegenerative diseases is particularly challenging because of the discrepancies in drug effects between in vitro and in vivo studies. These discrepancies occur in part because current cell culture systems used for drug screening have many limitations. First, few cell culture systems accurately model human aging or neurodegenerative diseases. Second, drug efficacy may differ between dividing and stationary cells, the latter resembling nondividing neurons in the CNS. Brain aggregates (BrnAggs) derived from embryonic day 15 gestation mouse embryos may represent neuropathogenic processes in prion disease and reflect in vivo drug efficacy. Here, we report a new method for the production of BrnAggs suitable for drug screening and suggest that BrnAggs can model additional neurological diseases such as tauopathies. We also report a functional assay with BrnAggs by measuring electrophysiological activities. Our data suggest that BrnAggs could serve as an effective in vitro cell culture system for drug discovery for neurodegenerative diseases.

Keywords: Brain aggregates; Dendritic degeneration; Drug screening; Neurodegeneration; Tau..

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Age Factors
  • Animals
  • Brain / cytology*
  • Cell Culture Techniques / methods*
  • Cells, Cultured
  • Embryo, Mammalian
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Transgenic
  • Models, Biological*
  • Nerve Net / drug effects
  • Nerve Net / physiology*
  • Neurodegenerative Diseases* / genetics
  • Neurodegenerative Diseases* / pathology
  • Neurodegenerative Diseases* / physiopathology
  • Neuroglia / physiology
  • Neurons / physiology
  • Pregnancy
  • Sodium Channel Blockers / pharmacology
  • tau Proteins / genetics
  • tau Proteins / metabolism

Substances

  • Sodium Channel Blockers
  • tau Proteins