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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-996204725656443fac59942e7ce110ae |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT ninahpipalia automatedmicroscopyscreeningforcompoundsthatpartiallyrevertcholesterolaccumulationinniemannpickccells AT amyhuang automatedmicroscopyscreeningforcompoundsthatpartiallyrevertcholesterolaccumulationinniemannpickccells AT haroldralph automatedmicroscopyscreeningforcompoundsthatpartiallyrevertcholesterolaccumulationinniemannpickccells AT madalinarujoi automatedmicroscopyscreeningforcompoundsthatpartiallyrevertcholesterolaccumulationinniemannpickccells AT frederickrmaxfield automatedmicroscopyscreeningforcompoundsthatpartiallyrevertcholesterolaccumulationinniemannpickccells |
_version_ |
1721506479942402048 |