Method for organotypic tissue culture in the aged animal

Jared Schommer, Matthew Schrag, Alexander Nackenoff, Gurdeep Marwarha, Othman Ghribi

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


Organotypic slicing of brain tissue from young rodents has been used as a powerful model system for biomedical research [1–3]. Organotypic slicing complements cell culture and in vivo studies in multiple facets. This system can be useful for investigating manipulation of cellular signaling pathways without the hindrance of the blood-brain barrier while sacrificing fewer animals in the process. It also allows for preserved cellular connectivity and local intact circuitry which is a drawback of isolated cell cultures. Studies on age-related diseases have mainly used embryonic or early postnatal organotypic slice tissue. Excluding synaptic plasticity studies that are usually carried-out over a few hours and use adult mice or rats, a handful of studies performed on adult animals have had success for survival of slices [4,5]. Here we describe a method for culturing organotypic slices with high viability from hippocampus of aged mice and rabbits. • Our method permits slices from mice as old as 16 months and rabbits as old as years of age to survive ex vivo up to 8 weeks [6–9]. Such a slice system may be relevant to investigating age-related brain diseases.

Original languageEnglish (US)
Pages (from-to)166-171
Number of pages6
StatePublished - 2017


  • Aged brain
  • Hippocampus
  • Organotypic slices

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Medical Laboratory Technology


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