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RESEARCH ARTICLE
Year : 2020  |  Volume : 15  |  Issue : 3  |  Page : 557-568

Trophic factors are essential for the survival of grafted oligodendrocyte progenitors and for neuroprotection after perinatal excitotoxicity


1 Intellectual and Developmental Disabilities Research Center, Jane and Terry Semel Institute for Neuroscience and Human Behavior, Departments of Neurobiology, Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, CA, USA
2 Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA

Correspondence Address:
Carlos Cepeda
Intellectual and Developmental Disabilities Research Center, Jane and Terry Semel Institute for Neuroscience and Human Behavior, Departments of Neurobiology, Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, CA
USA
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Source of Support: The Cell Culture Core supported by grant No. PP1498: Neural Cell Culture Core and NIH grant No. 04612 Intellectual & Developmental Disabilities. The Cell, Circuits and Systems Analysis Core is supported by NICHD award No. U54HD087101-03, Conflict of Interest: None


DOI: 10.4103/1673-5374.266066

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The consequences of neonatal white matter injury are devastating and represent a major societal problem as currently there is no cure. Prematurity, low weight birth and maternal pre-natal infection are the most frequent causes of acquired myelin deficiency in the human neonate leading to cerebral palsy and cognitive impairment. In the developing brain, oligodendrocyte (OL) maturation occurs perinatally, and immature OLs are particularly vulnerable. Cell replacement therapy is often considered a viable option to replace progenitors that die due to glutamate excitotoxicity. We previously reported directed specification and mobilization of endogenous committed and uncommitted neural progenitors by the combination of transferrin and insulin growth factor 1 (TSC1). Here, considering cell replacement and integration as therapeutic goals, we examined if OL progenitors (OLPs) grafted into the brain parenchyma of mice that were subjected to an excitotoxic insult could rescue white matter injury. For that purpose, we used a well-established model of glutamate excitotoxic injury. Four-day-old mice received a single intraparenchymal injection of the glutamate receptor agonist N-methyl-D-aspartate alone or in conjunction with TSC1 in the presence or absence of OLPs grafted into the brain parenchyma. Energetics and expression of stress proteins and OL developmental specific markers were examined. A comparison of the proteomic profile per treatment was also ascertained. We found that OLPs did not survive in the excitotoxic environment when grafted alone. In contrast, when combined with TSC1, survival and integration of grafted OLPs was observed. Further, energy metabolism in OLPs was significantly increased by N-methyl-D-aspartate and modulated by TSC1. The proteomic profile after the various treatments showed elevated ubiquitination and stress/heat shock protein 90 in response to N-methyl-D-aspartate. These changes were reversed in the presence of TSC1 and ubiquitination was decreased. The results obtained in this pre-clinical study indicate that the use of a combinatorial intervention including both trophic support and healthy OLPs constitutes a promising approach for long-term survival and successful graft integration. We established optimal conditioning of the host brain environment to promote long-term survival and integration of grafted OLPs into an inflamed neonate host brain. Experimental procedures were performed under the United States Public Health Service Guide for the Care and Use of Laboratory Animals and were approved by the Institutional Animal Care Committee at (UCLA) (ARC #1992-034-61) on July 1, 2010.


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