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      SC1, a brain extracellular matrix glycoprotein related to SPARC and follistatin, is expressed by rat cerebellar astrocytes following injury and during development.

      Brain Research
      Activated-Leukocyte Cell Adhesion Molecule, Aging, metabolism, Animals, Animals, Newborn, growth & development, Astrocytes, Blotting, Northern, Cerebellar Diseases, pathology, Cerebellum, cytology, Extracellular Matrix Proteins, genetics, Immunohistochemistry, In Situ Hybridization, Male, Nerve Tissue Proteins, RNA, Messenger, Rats, Rats, Wistar, Reference Values

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          Abstract

          In the nervous system, extracellular matrix components are believed to influence cell shape, proliferation and migration during development and following injury. SC1 is a secreted glycoprotein expressed during neural development and in the adult brain. The molecule shows partial sequence homology to the anti-adhesive extracellular matrix molecule SPARC/osteonectin and to follistatin. We have made a surgical lesion in the adult rat cerebellum and examined changes in SC1 expression at 1 to 14 days after injury. Dual in situ hybridization/immunohistochemistry demonstrated that SC1 mRNA was induced in astrocytes surrounding the wound, reaching maximal levels at 10 days post-lesion. Immunohistochemistry revealed changes in the deposition of SC1 protein in radial fibres of Bergmann glia. SC1 protein was also detected at the border of the lesion, suggesting an association with the glial scar. Double immunohistochemistry with the astrocytic marker GFAP demonstrated that astrocytes also express SC1 during postnatal development.

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