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Neurotrophically Induced Mesenchymal Progenitor Cells Derived from Induced Pluripotent Stem Cells Enhance Neuritogenesis via Neurotrophin and Cytokine Production.
- Source :
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Stem cells translational medicine [Stem Cells Transl Med] 2018 Jan; Vol. 7 (1), pp. 45-58. Date of Electronic Publication: 2017 Dec 07. - Publication Year :
- 2018
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Abstract
- Adult tissue-derived mesenchymal stem cells (MSCs) are known to produce a number of bioactive factors, including neurotrophic growth factors, capable of supporting and improving nerve regeneration. However, with a finite culture expansion capacity, MSCs are inherently limited in their lifespan and use. We examined here the potential utility of an alternative, mesenchymal-like cell source, derived from induced pluripotent stem cells, termed induced mesenchymal progenitor cells (MiMPCs). We found that several genes were upregulated and proteins were produced in MiMPCs that matched those previously reported for MSCs. Like MSCs, the MiMPCs secreted various neurotrophic and neuroprotective factors, including brain-derived neurotrophic factor (BDNF), interleukin-6 (IL-6), leukemia inhibitory factor (LIF), osteopontin, and osteonectin, and promoted neurite outgrowth in chick embryonic dorsal root ganglia (DRG) cultures compared with control cultures. Cotreatment with a pharmacological Trk-receptor inhibitor did not result in significant decrease in MiMPC-induced neurite outgrowth, which was however inhibited upon Jak/STAT3 blockade. These findings suggest that the MiMPC induction of DRG neurite outgrowth is unlikely to be solely dependent on BDNF, but instead Jak/STAT3 activation by IL-6 and/or LIF is likely to be critical neurotrophic signaling pathways of the MiMPC secretome. Taken together, these findings suggest MiMPCs as a renewable, candidate source of therapeutic cells and a potential alternative to MSCs for peripheral nerve repair, in view of their ability to promote nerve growth by producing many of the same growth factors and cytokines as Schwann cells and signaling through critical neurotrophic pathways. Stem Cells Translational Medicine 2018;7:45-58.<br /> (© 2017 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.)
- Subjects :
- Animals
Brain-Derived Neurotrophic Factor metabolism
Cell Line
Chick Embryo
Ganglia, Spinal cytology
Ganglia, Spinal growth & development
Humans
Induced Pluripotent Stem Cells cytology
Interleukin-6 metabolism
Leukemia Inhibitory Factor metabolism
Mesenchymal Stem Cells cytology
Neurites metabolism
Neurogenesis physiology
Osteonectin metabolism
Osteopontin metabolism
STAT3 Transcription Factor antagonists & inhibitors
Triterpenes pharmacology
Cytokines metabolism
Induced Pluripotent Stem Cells metabolism
Mesenchymal Stem Cells metabolism
Nerve Growth Factors metabolism
Nerve Regeneration physiology
Schwann Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2157-6564
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Stem cells translational medicine
- Publication Type :
- Academic Journal
- Accession number :
- 29215199
- Full Text :
- https://doi.org/10.1002/sctm.17-0108