Visualization of cholesterol deposits in lysosomes of Niemann-Pick type C fibroblasts using recombinant perfringolysin O.

ABSTRACT:

Background

Niemann-Pick disease type C (NPC) is caused by defects in cholesterol efflux from lysosomes due to mutations of genes coding for NPC1 and NPC2 proteins. As a result, massive accumulation of unesterified cholesterol in late endosomes/lysosomes is observed. At the level of the organism these cholesterol metabolism disorders are manifested by progressive neurodegeneration and hepatosplenomegaly. Until now filipin staining of cholesterol deposits in cells has been widely used for NPC diagnostics. In this report we present an alternative method for cholesterol visualization and estimation using a cholesterol-binding bacterial toxin, perfringolysin O.

Methods

To detect cholesterol deposits, a recombinant probe, perfringolysin O fused with glutathione S-transferase (GST-

SUBMITTER: Kwiatkowska K 

PROVIDER: S-EPMC4005833 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature