Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells

Niemann-Pick disease type C (NPC) is an autosomal recessive genetic disorder manifested by abnormal accumulation of unesterified cholesterol and other lipids. We screened combinatorially synthesized chemical libraries to identify compounds that would partially revert cholesterol accumulation. Cultur...

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Main Authors: Nina H. Pipalia, Amy Huang, Harold Ralph, Madalina Rujoi, Frederick R. Maxfield
Format: Article
Language:English
Published: Elsevier 2006-02-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520336294
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spelling doaj-996204725656443fac59942e7ce110ae2021-04-27T04:45:31ZengElsevierJournal of Lipid Research0022-22752006-02-01472284301Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cellsNina H. Pipalia0Amy Huang1Harold Ralph2Madalina Rujoi3Frederick R. Maxfield4Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021Niemann-Pick disease type C (NPC) is an autosomal recessive genetic disorder manifested by abnormal accumulation of unesterified cholesterol and other lipids. We screened combinatorially synthesized chemical libraries to identify compounds that would partially revert cholesterol accumulation. Cultured CHO cells with NPC phenotypes (CT60 and CT43) were used for screening along with normal CHO cells as a control. We developed an automated microscopy assay based on imaging of filipin fluorescence for estimating cholesterol accumulation in lysosomal storage organelles. Our primary screen of 14,956 compounds identified 14 hit compounds that caused significant reduction in cellular cholesterol accumulation at 10 μM. We then screened a secondary library of 3,962 compounds selected based on chemical similarity to the initial hits and identified 7 compounds that demonstrated greater efficacy and lower toxicity than the original hits. These compounds are effective at concentrations of 123 nM to 3 μM in reducing the cholesterol accumulation in cells with a NPC1 phenotype.http://www.sciencedirect.com/science/article/pii/S0022227520336294high-content screeningfilipinlysosomal storage
collection DOAJ
language English
format Article
sources DOAJ
author Nina H. Pipalia
Amy Huang
Harold Ralph
Madalina Rujoi
Frederick R. Maxfield
spellingShingle Nina H. Pipalia
Amy Huang
Harold Ralph
Madalina Rujoi
Frederick R. Maxfield
Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
Journal of Lipid Research
high-content screening
filipin
lysosomal storage
author_facet Nina H. Pipalia
Amy Huang
Harold Ralph
Madalina Rujoi
Frederick R. Maxfield
author_sort Nina H. Pipalia
title Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
title_short Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
title_full Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
title_fullStr Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
title_full_unstemmed Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells
title_sort automated microscopy screening for compounds that partially revert cholesterol accumulation in niemann-pick c cells
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2006-02-01
description Niemann-Pick disease type C (NPC) is an autosomal recessive genetic disorder manifested by abnormal accumulation of unesterified cholesterol and other lipids. We screened combinatorially synthesized chemical libraries to identify compounds that would partially revert cholesterol accumulation. Cultured CHO cells with NPC phenotypes (CT60 and CT43) were used for screening along with normal CHO cells as a control. We developed an automated microscopy assay based on imaging of filipin fluorescence for estimating cholesterol accumulation in lysosomal storage organelles. Our primary screen of 14,956 compounds identified 14 hit compounds that caused significant reduction in cellular cholesterol accumulation at 10 μM. We then screened a secondary library of 3,962 compounds selected based on chemical similarity to the initial hits and identified 7 compounds that demonstrated greater efficacy and lower toxicity than the original hits. These compounds are effective at concentrations of 123 nM to 3 μM in reducing the cholesterol accumulation in cells with a NPC1 phenotype.
topic high-content screening
filipin
lysosomal storage
url http://www.sciencedirect.com/science/article/pii/S0022227520336294
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