ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism

Oxysterol binding protein (OSBP) related proteins (ORPs) constitute a family that has at least 12 members in humans. In the present study we characterize one of the novel OSBP homologs, ORP2, which we show to be expressed ubiquitously in mammalian tissues. The ORP2 cDNA encodes a deduced 55 kDa prot...

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Main Authors: Saara Laitinen, Markku Lehto, Sanna Lehtonen, Kati Hyvärinen, Sanna Heino, Eero Lehtonen, Christian Ehnholm, Elina Ikonen, Vesa M. Olkkonen
Format: Article
Language:English
Published: Elsevier 2002-02-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520301668
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spelling doaj-73e419799b1c45b2b6cb5f7f0c5d5c592021-04-27T04:38:19ZengElsevierJournal of Lipid Research0022-22752002-02-01432245255ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolismSaara Laitinen0Markku Lehto1Sanna Lehtonen2Kati Hyvärinen3Sanna Heino4Eero Lehtonen5Christian Ehnholm6Elina Ikonen7Vesa M. Olkkonen8Department of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandDepartment of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandDepartment of Pathology, Haartman-Institute, P.O. Box 21, FIN-00014, University of Helsinki, FinlandDepartment of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandDepartment of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandDepartment of Pathology, Haartman-Institute, P.O. Box 21, FIN-00014, University of Helsinki, FinlandDepartment of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandDepartment of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandTo whom correspondence should be addressed.; Department of Molecular Medicine, National Public Health Institute, Biomedicum, P.O. Box 104, FIN-00251 Helsinki, FinlandOxysterol binding protein (OSBP) related proteins (ORPs) constitute a family that has at least 12 members in humans. In the present study we characterize one of the novel OSBP homologs, ORP2, which we show to be expressed ubiquitously in mammalian tissues. The ORP2 cDNA encodes a deduced 55 kDa protein that lacks a pleckstrin homology (PH) domain, a feature found in the other family members. Sucrose gradient centrifugation analysis of Chinese hamster ovary (CHO) cell post-nuclear supernatant demonstrated that ORP2 is distributed in soluble and membrane-bound fractions. Immunofluorescence microscopy of the endogenous and overexpressed ORP2 in CHO cells suggested that the membrane-bound fraction of the protein localizes to the Golgi apparatus. Stably transfected CHO cells that overexpress ORP2 showed an increase in [14C]cholesterol efflux to serum, apolipoprotein A-I (apoA-I), and phosphatidyl choline vesicles. The proportion of cellular [14C]cholesterol that is esterified and the ACAT activity measured as [14C]oleyl-CoA conversion into cholesteryl [14C]oleate by the cellular membranes, were markedly decreased in the ORP2 expressing cells. Transient high level overexpression of ORP2 interfered with the clearance of a secretory pathway protein marker from the Golgi complex. The results implicate ORP2 as a novel regulator of cellular sterol homeostasis and intracellular membrane trafficking.—Laitinen, S., M. Lehto, S. Lehtonen, K. Hyvärinen, S. Heino, E. Lehtonen, C. Ehnholm, E. Ikonen, and V. M. Olkkonen. ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism.http://www.sciencedirect.com/science/article/pii/S0022227520301668cholesterol effluxcholesterol esterificationGolgi apparatusmRNA expressionprotein expressionmembrane trafficking
collection DOAJ
language English
format Article
sources DOAJ
author Saara Laitinen
Markku Lehto
Sanna Lehtonen
Kati Hyvärinen
Sanna Heino
Eero Lehtonen
Christian Ehnholm
Elina Ikonen
Vesa M. Olkkonen
spellingShingle Saara Laitinen
Markku Lehto
Sanna Lehtonen
Kati Hyvärinen
Sanna Heino
Eero Lehtonen
Christian Ehnholm
Elina Ikonen
Vesa M. Olkkonen
ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
Journal of Lipid Research
cholesterol efflux
cholesterol esterification
Golgi apparatus
mRNA expression
protein expression
membrane trafficking
author_facet Saara Laitinen
Markku Lehto
Sanna Lehtonen
Kati Hyvärinen
Sanna Heino
Eero Lehtonen
Christian Ehnholm
Elina Ikonen
Vesa M. Olkkonen
author_sort Saara Laitinen
title ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
title_short ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
title_full ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
title_fullStr ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
title_full_unstemmed ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
title_sort orp2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2002-02-01
description Oxysterol binding protein (OSBP) related proteins (ORPs) constitute a family that has at least 12 members in humans. In the present study we characterize one of the novel OSBP homologs, ORP2, which we show to be expressed ubiquitously in mammalian tissues. The ORP2 cDNA encodes a deduced 55 kDa protein that lacks a pleckstrin homology (PH) domain, a feature found in the other family members. Sucrose gradient centrifugation analysis of Chinese hamster ovary (CHO) cell post-nuclear supernatant demonstrated that ORP2 is distributed in soluble and membrane-bound fractions. Immunofluorescence microscopy of the endogenous and overexpressed ORP2 in CHO cells suggested that the membrane-bound fraction of the protein localizes to the Golgi apparatus. Stably transfected CHO cells that overexpress ORP2 showed an increase in [14C]cholesterol efflux to serum, apolipoprotein A-I (apoA-I), and phosphatidyl choline vesicles. The proportion of cellular [14C]cholesterol that is esterified and the ACAT activity measured as [14C]oleyl-CoA conversion into cholesteryl [14C]oleate by the cellular membranes, were markedly decreased in the ORP2 expressing cells. Transient high level overexpression of ORP2 interfered with the clearance of a secretory pathway protein marker from the Golgi complex. The results implicate ORP2 as a novel regulator of cellular sterol homeostasis and intracellular membrane trafficking.—Laitinen, S., M. Lehto, S. Lehtonen, K. Hyvärinen, S. Heino, E. Lehtonen, C. Ehnholm, E. Ikonen, and V. M. Olkkonen. ORP2, a homolog of oxysterol binding protein, regulates cellular cholesterol metabolism.
topic cholesterol efflux
cholesterol esterification
Golgi apparatus
mRNA expression
protein expression
membrane trafficking
url http://www.sciencedirect.com/science/article/pii/S0022227520301668
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