| Literature DB >> 14530298 |
Björn Scheffler1, Tanja Schmandt, Wolfgang Schröder, Barbara Steinfarz, Leila Husseini, Jörg Wellmer, Gerald Seifert, Khalad Karram, Heinz Beck, Ingmar Blümcke, Otmar D Wiestler, Christian Steinhäuser, Oliver Brüstle.
Abstract
Embryonic stem (ES) cells provide attractive prospects for neural transplantation. So far, grafting strategies in the CNS have focused mainly on neuronal replacement. Employing a slice culture model, we found that ES cell-derived glial precursors (ESGPs) possess a remarkable capacity to integrate into the host glial network. Following deposition on the surface of hippocampal slices, ESGPs actively migrate into the recipient tissue and establish extensive cell-cell contacts with recipient glia. Gap junction-mediated coupling between donor and host astrocytes permits widespread delivery of dye from single donor cells. During maturation, engrafted donor cells display morphological, immunochemical and electrophysiological properties that are characteristic of differentiating native glia. Our findings provide the first evidence of functional integration of grafted astrocytes, and depict glial network integration as a potential route for widespread transcellular delivery of small molecules to the CNS.Entities:
Mesh:
Year: 2003 PMID: 14530298 DOI: 10.1242/dev.00714
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868