Astrocytes originated from neural stem cells drive the regenerative remodeling of pathologic CSPGs in spinal cord injury

Stem Cell Reports. 2024 Oct 8;19(10):1451-1473. doi: 10.1016/j.stemcr.2024.08.007. Epub 2024 Sep 19.

Abstract

Neural degeneration is a hallmark of spinal cord injury (SCI). Multipotent neural precursor cells (NPCs) have the potential to reconstruct the damaged neuron-glia network due to their tri-lineage capacity to generate neurons, astrocytes, and oligodendrocytes. However, astrogenesis is the predominant fate of resident or transplanted NPCs in the SCI milieu adding to the abundant number of resident astrocytes in the lesion. How NPC-derived astrocytes respond to the inflammatory milieu of SCI and the mechanisms by which they contribute to the post-injury recovery processes remain largely unknown. Here, we uncover that activated NPC-derived astrocytes exhibit distinct molecular signature that is immune modulatory and foster neurogenesis, neuronal maturity, and synaptogenesis. Mechanistically, NPC-derived astrocytes perform regenerative matrix remodeling by clearing inhibitory chondroitin sulfate proteoglycans (CSPGs) from the injury milieu through LAR and PTP-σ receptor-mediated endocytosis and the production of ADAMTS1 and ADAMTS9, while most resident astrocytes are pro-inflammatory and contribute to the pathologic deposition of CSPGs. These novel findings unravel critical mechanisms of NPC-mediated astrogenesis in SCI repair.

Keywords: CSPGs remodeling; LAR and PTP-σ receptors; astrocytes; neural precursor cells; neurogenesis; spinal cord injury.

MeSH terms

  • Animals
  • Astrocytes* / metabolism
  • Cell Differentiation
  • Chondroitin Sulfate Proteoglycans* / metabolism
  • Mice
  • Neural Stem Cells* / cytology
  • Neural Stem Cells* / metabolism
  • Neurogenesis
  • Neurons / metabolism
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2 / metabolism
  • Spinal Cord Injuries* / metabolism
  • Spinal Cord Injuries* / pathology

Substances

  • Chondroitin Sulfate Proteoglycans
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2