4.8 Article

Expansion of murine and human olfactory epithelium/mucosa colonies and generation of mature olfactory sensory neurons under chemically defined conditions

Journal

THERANOSTICS
Volume 11, Issue 2, Pages 684-699

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/thno.46750

Keywords

Olfactory epithelium/mucosa; three-dimensional culture; colony; Lgr5; olfactory sensory neurons

Funding

  1. National Natural Science Foundation of China [81700894, 31771155, 81970856, 31900714, 31800826]
  2. Shanghai Municipal Education Commission
  3. Shanghai Eastern Scholar Program [TP2016029]
  4. Shanghai Municipal Human Resources and Social Security Bureau, Shanghai Talent Development Fund [2018112]
  5. China Postdoctoral Science Foundation [2020M671728]

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Research suggests that olfactory stem cells may be a promising tool for replacing inactive globose basal cells and generating sensory neurons, potentially providing a new source for cell replacement-based therapy against smell loss.
Olfactory dysfunctions, including hyposmia and anosmia, affect similar to 100 million people around the world and the underlying causes are not fully understood. Degeneration of olfactory sensory neurons and incapacity of globose basal cells to generate olfactory sensory neurons are found in elder people and patients with smell disorders. Thus, olfactory stem cell may function as a promising tool to replace inactivated globose basal cells and to generate sensory neurons. Methods: We established clonal expansion of cells from the murine olfactory epithelium as well as colony growth from human olfactory mucosa using Matrigel-based three-dimensional system. These colonies were characterized by immunostaining against olfactory epithelium cellular markers and by calcium imaging of responses to odors. Chemical addition was optimized to promote Lgr5 expression, colony growth and sensory neuron generation, tested by quantitative PCR and immunostaining against progenitor and neuronal markers. The differential transcriptomes in multiple signaling pathways between colonies under different base media and chemical cocktails were determined by RNA-Seq. Results: In defined culture media, we found that VPA and CHIR99021 induced the highest Lgr5 expression level, while LY411575 resulted in the most abundant yield of OMP+ mature sensory neurons in murine colonies. Different base culture media with drug cocktails led to apparent morphological alteration from filled to cystic appearance, accompanied with massive transcriptional changes in multiple signaling pathways. Generation of sensory neurons in human colonies was affected through TGF-beta signaling, while Lgr5 expression and cell proliferation was regulated by VPA. Conclusion: Our findings suggest that targeting expansion of olfactory epithelium/mucosa colonies in vitro potentially results in discovery of new source to cell replacement-based therapy against smell loss.

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