Genetic modification increases the survival and the neuroregenerative properties of transplanted neural stem cells

JCI Insight. 2020 Feb 27;5(4):e126268. doi: 10.1172/jci.insight.126268.

Abstract

Cell therapy raises hopes high for better treatment of brain disorders. However, the majority of transplanted cells often die soon after transplantation, and those that survive initially continue to die in the subacute phase, diminishing the impact of transplantations. In this study, we genetically modified transplanted human neural stem cells (hNSCs), from 2 distant embryonic stem cell lines (H9 and RC17), to express 1 of 4 prosurvival factors - Hif1a, Akt1, Bcl-2, or Bcl-xl - and studied how these modifications improve short- and long-term survival of transplanted hNSCs. All genetic modifications dramatically increased survival of the transplanted hNSCs. Importantly, 3 out of 4 modifications also enhanced the exit of hNSCs from the cell cycle, thus avoiding aberrant growth of the transplants. Bcl-xl expression provided the strongest protection of transplanted cells, reducing both immediate and delayed cell death, and stimulated hNSC differentiation toward neuronal and oligodendroglial lineages. By designing hNSCs with drug-controlled expression of Bcl-xl, we demonstrated that short-term expression of a prosurvival factor can ensure the long-term survival of transplanted cells. Importantly, transplantation of Bcl-xl-expressing hNSCs into mice suffering from stroke improved behavioral outcome and recovery of motor activity in mice.

Keywords: Apoptosis; Neuronal stem cells; Neuroscience; Stem cell transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Differentiation*
  • Cell Survival / genetics*
  • Humans
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Motor Activity
  • Neural Stem Cells / cytology*
  • Stem Cell Transplantation*
  • Stroke / metabolism
  • Stroke / pathology*
  • Treatment Outcome
  • bcl-X Protein / genetics

Substances

  • BCL2L1 protein, human
  • bcl-X Protein

Grant support

to KK