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J Biol Chem, Vol. 274, Issue 36, 25455-25460, September 3, 1999

Heparin Is a Unique Marker of Progenitors in the Glial Cell Lineage

Sally E. StringerDagger , Margot Mayer-Proschel, Anjali Kalyaniparallel , Mahendra Raoparallel , and John T. Gallagher**

From the Cancer Research Campaign, Dagger  Drug Development and Imaging Section, Paterson Institute of Cancer Research and the ** Medical Oncology Department (University of Manchester), Christie Hospital, Wilmslow Road, Manchester M20 4BX, United Kingdom, the  Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah 84112, and the parallel  Department of Neurobiology and Anatomy, University of Utah Medical School, Salt Lake City, Utah 84132

The oligodendrocyte-type-2 astrocyte progenitor cells (precursors of oligodendrocytes and type-2 astrocytes) are an excellent system in which to study differentiation as they can be manipulated in vitro. Maintenance of oligodendrocyte-type-2 astrocyte progenitor cells requires basic fibroblast growth factor, a growth factor whose action normally depends on a heparan sulfate coreceptor. Biochemical analysis revealed a most surprising result: that the oligodendrocyte-type-2 astrocyte progenitors did not synthesize heparan sulfate, the near ubiquitous N-sulfated cell surface polysaccharide, but the chemically related heparin in a form that was almost completely N- and O-sulfated. The heparin was detected in the pericellular fraction of the cells and the culture medium. In contrast the differentiated glial subpopulations (oligodendrocytes and type-2 astrocytes) synthesized typical heparan sulfate but with distinctive fine structural features for each cell type. Thus heparin is a unique differentiation marker in the glial lineage. Previously heparin has been found only in a subset of mature mast cells called the connective tissue mast cells. Its presence within the developing nervous system on a precise population of progenitors may confer specific and essential recognition properties on those cells in relation to binding soluble growth and/or differentiation factors and the extracellular matrix.


Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.



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