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Generation of a LacZ reporter transgenic mouse line for the stereological analysis of oligodendrocyte loss in galactosylceramidase deficiency

  • Hongling Zhu
  • , Francesca Ornaghi
  • , Sophie Belin
  • , Maria I. Givogri
  • , Lawrence Wrabetz
  • , Ernesto R. Bongarzone
  • University of Illinois at Chicago
  • San Raffaele Scientific Institute
  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Krabbe's disease is a leukodystrophy resulting from deficiency of galactosylceramidase and the accumulation of galactosylsphingosine (psychosine) in the nervous system. Psychosine is believed to cause central demyelination by killing oligodendrocytes. Quantitative analysis of this process is lacking. To address this, we generated a new transgenic reporter twitcher line in which myelinating oligodendrocytes are genetically marked by the expression of LacZ under control of the myelin basic protein (MBP) promoter. MBP-LacZ-twitcher transgenic mice were used for unbiased stereological quantification of β-galactosidase+ oligodendrocytes in the spinal cord. As expected, we found decreased numbers of these cells in mutant cords, paralleling the severity of clinical disease. The decrease of oligodendrocytes does not correlate well with the increase of psychosine. The new MBP-LacZ-twitcher line will be a useful genetic tool for measuring changes in oligodendrocyte numbers in different regions of the mutant CNS and in preclinical trials of therapies to prevent demyelination.

Original languageEnglish
Pages (from-to)1520-1530
Number of pages11
JournalJournal of Neuroscience Research
Volume94
Issue number12
DOIs
StatePublished - Dec 1 2016

Keywords

  • demyelination
  • Krabbe's disease
  • oligodendrocytes
  • psychosine

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