Decline in arylsulfatase B and Increase in chondroitin 4-sulfotransferase combine to increase chondroitin 4-sulfate in traumatic brain injury

Sumit Bhattacharyya, Xiaolu Zhang, Leo Feferman, David Johnson, Frank C. Tortella, Marina Guizzetti, Joanne K. Tobacman

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

In an established rat model of penetrating ballistic-like brain injury (PBBI), arylsulfatase B (ARSB; N-acetylgalactosamine 4-sulfatase) activity was significantly reduced at the ipsilateral site of injury, but unaffected at the contralateral site or in sham controls. In addition, the ARSB substrate chondroitin 4-sulfate (C4S) and total sulfated glycosaminoglycans increased. The mRNA expression of chondroitin 4-sulfotransferase 1 (C4ST1; CHST11) and the sulfotransferase activity rose at the ipsilateral site of injury (PBBI-I), indicating contributions from both increased production and reduced degradation to the accumulation of C4S. In cultured, fetal rat astrocytes, following scratch injury, the ARSB activity declined and the nuclear hypoxia inducible factor-1α increased significantly. In contrast, sulfotransferase activity and chondroitin 4-sulfotransferase expression increased following astrocyte exposure to TGF-β1, but not following scratch. These different pathways by which C4S increased in the cell preparations were both evident in the response to injury in the PBBI-I model. Hence, findings support effects of injury because of mechanical disruption inhibiting ARSB and to chemical mediation by TGF-β1 increasing CHST11 expression and sulfotransferase activity. The increase in C4S following traumatic brain injury is because of contributions from impaired degradation and enhanced synthesis of C4S which combine in the pathogenesis of the glial scar.

Original languageEnglish (US)
Pages (from-to)728-739
Number of pages12
JournalJournal of Neurochemistry
Volume134
Issue number4
DOIs
StatePublished - Aug 1 2015

Keywords

  • CHST11
  • arylsulfatase B
  • astrocytes
  • chondroitin 4-sulfate
  • glycosaminoglycans
  • neurocan

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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