Administration of prosaposin-derived neurotrophic factor to neural tube defects facilitates regeneration and restores neurological functions
Neural tube defects (NTDs) cause fetal and pediatric deaths or lifelong neurological disabilities. No effective treatment is currently available for NTDs. We attempted to elucidate the pathogenesis of NTDs and propose a therapeutic strategy. Intra-amniotic treatment with prosaposin-derived 18-mer pe...
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Veröffentlicht in: | iScience 2023-04, Vol.26 (4), p.106277-106277, Article 106277 |
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Sprache: | eng |
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Zusammenfassung: | Neural tube defects (NTDs) cause fetal and pediatric deaths or lifelong neurological disabilities. No effective treatment is currently available for NTDs. We attempted to elucidate the pathogenesis of NTDs and propose a therapeutic strategy. Intra-amniotic treatment with prosaposin-derived 18-mer peptide (PS18) protected the spinal cord from secondary damage and rescued neurological function in an established chicken model of spina bifida aperta (SBA), the severe type of NTDs. PS18 promoted the formation of a neuroectodermal covering over the defective neural tube within 24-h after treatment, enhanced the regeneration/restoration process, and decreased apoptotic activity in the developing spinal cord. PS18 reduced the SBA wound and almost completely formed the spinal cord. SBA chicks that received PS18 exhibited relatively normal walking and sensorimotor responses, and reduced pain-associated behavior in postnatal life. In conclusion, PS18 is a promising therapeutic agent for NTDs and may be useful for treating other types of spinal cord injuries.
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•We elucidated the early pathogenesis of neural tube defects related to leg dysfunctions•PS18 promoted to develop a neuroectodermal covering over the defective neural tube•PS18 enhanced the regeneration process and restored the neural tube by 24 h after treatment•PS18 protected the spinal cord from secondary damages and rescued motor functions
Molecular physiology; Neuroscience; Developmental biology |
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ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2023.106277 |