PMID- 15907942 OWN - NLM STAT- MEDLINE DCOM- 20050822 LR - 20231120 IS - 0022-510X (Print) IS - 0022-510X (Linking) VI - 233 IP - 1-2 DP - 2005 Jun 15 TI - Neural stem cells as a potential source of oligodendrocytes for myelin repair. PG - 179-81 AB - Neural stem cells (NSCs) are considered to have widespread therapeutic possibilities on account of their ability to provide large numbers of cells whilst retaining multi-potentiality. Application to human demyelinating diseases requires improved understanding of the signalling requirements underlying the generation of oligodendrocytes from NSCs. During development, spinal cord oligodendrocyte precursors (OPCs) originate from the ventral, but not dorsal neuroepithelium due to the regulatory effects of the morphogen Sonic hedgehog (Shh). The developing human spinal cord shows comparable ventral-dorsal gradient of oligodendrocyte differentiation potential to the embryonic rodent spinal cord. In contrast expanded human neural precursors derived from both isolated ventral or dorsal cultures show a reduced capacity to generate oligodendrocytes, whereas comparable rodent cultures demonstrate a marked increase in oligodendrocyte formation by a hedgehog independent pathway. Inter-species difference in the capacity of neural precursors to generate oligodendrocytes emphasises the need for greater study of human derived stem cell populations. FAU - Chandran, Siddharthan AU - Chandran S AD - Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. sc222@cam.ac.uk FAU - Compston, Alastair AU - Compston A LA - eng PT - Journal Article PT - Review PL - Netherlands TA - J Neurol Sci JT - Journal of the neurological sciences JID - 0375403 SB - IM MH - Animals MH - Cell Differentiation/physiology MH - Demyelinating Diseases/*therapy MH - Humans MH - Myelin Sheath/*metabolism MH - Neurons/cytology/*transplantation MH - Oligodendroglia/*physiology MH - Stem Cells/*physiology MH - Wound Healing/physiology RF - 33 EDAT- 2005/05/24 09:00 MHDA- 2005/08/23 09:00 CRDT- 2005/05/24 09:00 PHST- 2005/05/24 09:00 [pubmed] PHST- 2005/08/23 09:00 [medline] PHST- 2005/05/24 09:00 [entrez] AID - S0022-510X(05)00103-6 [pii] AID - 10.1016/j.jns.2005.03.019 [doi] PST - ppublish SO - J Neurol Sci. 2005 Jun 15;233(1-2):179-81. doi: 10.1016/j.jns.2005.03.019.