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Aberrant production of tenascin-C in globoid cell leukodystrophy alters psychosine-induced microglial functions.


ABSTRACT: Globoid cell leukodystrophy (GLD), or Krabbe disease, is a rare and often fatal demyelinating disease caused by mutations in the galactocerebrosidase (galc) gene that result in accumulation of galactosylsphingosine (psychosine). We recently reported that the extracellular matrix (ECM) protease, matrix metalloproteinase-3, is elevated in GLD and that it regulates psychosine-induced microglial activation. Here, we examined central nervous system ECM component expression in human GLD patients and in the twitcher mouse model of GLD using immunohistochemistry. The influence of ECM proteins on primary murine microglial responses to psychosine was evaluated using ECM proteins as substrates and analyzed by quantitative real-time polymerase chain reaction, immunocytochemistry, and ELISA. Functional

SUBMITTER: Claycomb KI 

PROVIDER: S-EPMC4169335 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

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