Concise Review: Human Pluripotent Stem Cells in the Treatment of Spinal Cord Injury

Author:

Lukovic Dunja1,Moreno Manzano Victoria2,Stojkovic Miodrag34,Bhattacharya Shom Shanker1,Erceg Slaven15

Affiliation:

1. CABIMER (Centro Andaluz de Biología Molecular y Medicina Regenerativa), Avda. Americo Vespucio s/n, Parque Científico y Tecnológico Cartuja, Sevilla, Spain

2. Neural Regeneration Lab, Centro de Investigación “Principe Felipe,” Valencia, Spain

3. Spebo Medical, Leskovac, Serbia

4. Human Genetics Department, Medical Faculty, University of Kragujevac, Kragujevac, Serbia

5. Medical Genome Project, Edificio INSUR, Parque Científico y Tecnológico Cartuja, Sevilla, Spain

Abstract

Abstract Spinal cord injury (SCI) results in neural loss and consequently motor and sensory impairment below the injury. There are currently no effective therapies for the treatment of traumatic SCI in humans. Different kinds of cells including embryonic, fetal, and adult stem cells have been transplanted into animal models of SCI resulting in sensorimotor benefits. Transplantation of human embryonic stem cell (hESC)- or induced pluripotent stem cell (hiPSC)-derived neural cells is nowadays a promising therapy for SCI. This review updates the recent progress in preclinical studies and discusses the advantages and flaws of various neural cell types derived from hESCs and hiPSCs. Before introducing the stem cell replacement strategies in clinical practice, this complex field needs to advance significantly in understanding the lesion itself, the animal model adequacy, and improve cell replacement source. This knowledge will contribute to the successful translation from animals to humans and lead to established guidelines for rigorous safety screening in order to be implemented in clinical practice.

Funder

Miguel Servet

Instituto de Salud Carlos III of Spanish Ministry of Science and Innovation

Health of Spain

Junta de Andalucia

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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