ARP2/3 complex is required for directional migration of neural stem cell-derived oligodendrocyte precursors in electric fields

dc.contributor.authorLi, Yongchao
dc.contributor.authorWang, Pei-Shan
dc.contributor.authorLucas, George
dc.contributor.authorLi, Rong
dc.contributor.authorYao, Li
dc.date.accessioned2015-05-15T20:23:43Z
dc.date.available2015-05-15T20:23:43Z
dc.date.issued2015-03-21
dc.descriptionClick on the DOI link to access the article (may not be free).en_US
dc.description.abstractIntroduction: The loss of oligodendrocytes in a lesion of the central nervous system causes demyelination and therefore impairs axon function and survival. Transplantation of neural stem cell-derived oligodendrocyte precursor cells (NSC-OPCs) results in increased oligodendrocyte formation and enhanced remyelination. The directional migration of grafted cells to the target can promote the establishment of functional reconnection and myelination in the process of neural regeneration. Endogenous electric fields (EFs) that were detected in the development of the central nervous system can regulate cell migration. Methods: NSCs were isolated from the brains of ARPC2(+/+) and ARPC2(-/-) mouse embryo and differentiated into OPCs. After differentiation, the cultured oligospheres were stimulated with EFs (50, 100, or 200 mV/mm). The migration of OPCs from oligospheres was recorded using time-lapse microscopy. The cell migration directedness and speed were analyzed and quantified. Results: In this study, we found that NSC-OPCs migrated toward the cathode pole in EFs. The directedness and displacement of cathodal migration increased significantly when the EF strength increased from 50 to 200 mV/mm. However, the EF did not significantly change the cell migration speed. We also showed that the migration speed of ARPC2(-/-) OPCs, deficient in the actin-related proteins 2 and 3 (ARP2/3) complex, was significantly lower than that of wild type of OPCs. ARPC2(-/-) OPCs migrated randomly in EFs. Conclusions: The migration direction of NSC-OPCs can be controlled by EFs. The function of the ARP complex is required for the cathodal migration of NSC-OPCs in EFs. EF-guided cell migration is an effective model to understanding the intracellular signaling pathway in the regulation of cell migration directness and motility.en_US
dc.description.sponsorshipThis work was supported by LY's start-up funding, Wichita State University, and an Institutional Development Award from the National Institute of General Medical Sciences of the National Institutes of Health under grants P20 GM103418 (to LY) and NIH PO1 GM066311 (to RL).en_US
dc.identifier.citationLi, Yongchao; Wang, Pei-Shan; Lucas, George; Li, Rong; Yao, Li. 2015. ARP2/3 complex is required for directional migration of neural stem cell-derived oligodendrocyte precursors in electric fields. Stem Cell Research & Therapy, vol. 6:article 41en_US
dc.identifier.issn1757-6512
dc.identifier.otherWOS:000353280900001
dc.identifier.urihttp://dx.doi.org/10.1186/s13287-015-0042-0
dc.identifier.urihttp://hdl.handle.net/10057/11274
dc.language.isoen_USen_US
dc.publisherBioMed Central Ltden_US
dc.relation.ispartofseriesStem Cell Research & Therapy;v.6:article41
dc.rights.holder© 2015 BioMed Central Ltd unless otherwise stated.
dc.subjectCorneal epithelial-cellsen_US
dc.subjectDirected migrationen_US
dc.subjectMechanismsen_US
dc.subjectExtensionen_US
dc.subjectDynamicsen_US
dc.subjectEmbryoen_US
dc.subjectRACen_US
dc.titleARP2/3 complex is required for directional migration of neural stem cell-derived oligodendrocyte precursors in electric fieldsen_US
dc.typeArticleen_US
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.6 KB
Format:
Item-specific license agreed upon to submission
Description: