Sexual dimorphisms in adult human neural, mesoderm-derived, and neural crest-derived stem cells

FEBS Lett. 2019 Dec;593(23):3338-3352. doi: 10.1002/1873-3468.13606. Epub 2019 Oct 2.

Abstract

Sexual dimorphisms contribute, at least in part, to the severity and occurrence of a broad range of neurodegenerative, cardiovascular, and bone disorders. In addition to hormonal factors, increasing evidence suggests that stem cell-intrinsic mechanisms account for sex-specific differences in human physiology and pathology. Here, we discuss sex-related intrinsic mechanisms in adult stem cell populations, namely mesoderm-derived stem cells, neural stem cells (NSCs), and neural crest-derived stem cells (NCSCs), and their implications for stem cell differentiation and regeneration. We particularly focus on sex-specific differences in stem cell-mediated bone regeneration, in neuronal development, and in NSC-mediated neuroprotection. Moreover, we review our own recently published observations regarding the sex-dependent role of NF-κB-p65 in neuroprotection of human NCSC-derived neurons and sex differences in NCSC-related disorders, so-called neurocristopathies. These observations are in accordance with the increasing evidence pointing toward sex-specific differences in neurocristopathies and degenerative diseases like Parkinson's disease or osteoporosis. All findings discussed here indicate that sex-specific variability in stem cell biology may become a crucial parameter for the design of future treatment strategies.

Keywords: NF-κB; mesoderm-derived stem cells; neural crest-derived stem cells; neural stem cells; neurocristopathies; neuroprotection; sex-specific differences; stem cells.

Publication types

  • Review

MeSH terms

  • Cell Differentiation / genetics
  • Female
  • Humans
  • Male
  • Mesoderm / growth & development*
  • Mesoderm / metabolism
  • NF-kappa B / genetics
  • Neural Crest / growth & development
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Neurons / metabolism
  • Osteoporosis / genetics*
  • Osteoporosis / pathology
  • Parkinson Disease / genetics*
  • Parkinson Disease / pathology
  • Sex Characteristics*
  • eIF-2 Kinase / genetics

Substances

  • NF-kappa B
  • eIF-2 Kinase