Cell-Based Therapy Restores Olfactory Function in an Inducible Model of Hyposmia

Stem Cell Reports. 2019 Jun 11;12(6):1354-1365. doi: 10.1016/j.stemcr.2019.05.001. Epub 2019 May 30.

Abstract

Stem cell-based therapies have been proposed as a strategy to replace damaged tissues, especially in the nervous system. A primary sensory modality, olfaction, is impaired in 12% of the US population, but lacks treatment options. We report here the development of a novel mouse model of inducible hyposmia and demonstrate that purified tissue-specific stem cells delivered intranasally engraft to produce olfactory neurons, achieving recovery of function. Adult mice were rendered hyposmic by conditional deletion of the ciliopathy-related IFT88 gene in the olfactory sensory neuron lineage and following experimentally induced olfactory injury, received either vehicle or stem cell infusion intranasally. Engraftment-derived olfactory neurons were identified histologically, and functional improvements were measured via electrophysiology and behavioral assay. We further explored mechanisms in culture that promote expansion of engraftment-competent adult olfactory basal progenitor cells. These findings provide a basis for translational research on propagating adult tissue-specific sensory progenitor cells and testing their therapeutic potential.

Keywords: anosmia; ciliopathy; neuron; olfaction; stem cells.

Publication types

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

MeSH terms

  • Animals
  • Benzilates
  • Ciliopathies* / genetics
  • Ciliopathies* / metabolism
  • Ciliopathies* / pathology
  • Ciliopathies* / therapy
  • Mice, Transgenic
  • Neural Stem Cells* / metabolism
  • Neural Stem Cells* / pathology
  • Neural Stem Cells* / transplantation
  • Olfaction Disorders* / genetics
  • Olfaction Disorders* / metabolism
  • Olfaction Disorders* / pathology
  • Olfaction Disorders* / therapy
  • Olfactory Receptor Neurons* / metabolism
  • Olfactory Receptor Neurons* / pathology
  • Smell*
  • Stem Cell Transplantation*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism

Substances

  • Benzilates
  • Tg737Rpw protein, mouse
  • Tumor Suppressor Proteins
  • propiverine