Neuroprotective effects of oligodendrocyte precursor cells on white matter damage in preterm infants.
- Author:
Yan YUE
1
;
Li ZHANG
;
Yi QU
;
De-Zhi MU
Author Information
1. Department of Pediatrics, West China Second University Hospital/Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu 610041, China. mudz@scu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Cell Separation;
Demyelinating Diseases;
therapy;
Humans;
Infant, Newborn;
Infant, Premature;
Oligodendrocyte Precursor Cells;
transplantation;
White Matter;
pathology
- From:
Chinese Journal of Contemporary Pediatrics
2018;20(4):326-331
- CountryChina
- Language:Chinese
-
Abstract:
White matter damage, characterized by demyelination due to the damage of oligodendrocyte precursor cells (OPCs), is the most common type of brain damage in preterm infants. Survivors are often subject to long-term neurodevelopmental sequelae because of the lack of effective treatment. In recent years, it has been found that cell transplantation has the potential for the treatment of white matter damage. OPCs are frequently used cells in cell transplantation therapy. With abilities of migration and myelinization, OPCs are the best seed cells for the treatment of white matter damage. Several studies have found that OPCs may not only replace impaired cells to reconstruct the structure and function of white matter, but also inhibit neuronal apoptosis, promote the proliferation of endogenous neural stem cells, and enhance the repairment of the blood-brain barrier. However, the clinical application of OPC transplantation therapy faces many challenges, such as the effectiveness, risk of tumorigenesis and immune rejection. With reference to these studies, this article reviewed the development of myelination, the obtainment of OPCs, the therapeutic mechanism as well as application research, and analyzed the current challenges of OPC transplantation, in order to provide a new direction for clinical treatment of white matter damage in preterm infants.
