Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2007;38:1791-1798
Published online before print April 19, 2007, doi: 10.1161/STROKEAHA.106.478867
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/6/1791    most recent
STROKEAHA.106.478867v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nuotio, K.
Right arrow Articles by Lindsberg, P. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nuotio, K.
Right arrow Articles by Lindsberg, P. J.
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*HomoloGene*UniGene
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Carotid Artery Disease
Hazardous Substances DB
*CHOLESTEROL
Related Collections
Right arrow Other arteriosclerosis
Right arrow Carotid Stenosis
Right arrow Other Stroke
Right arrow Other Vascular biology

(Stroke. 2007;38:1791.)
© 2007 American Heart Association, Inc.


Original Contributions

Adipophilin Expression Is Increased in Symptomatic Carotid Atherosclerosis

Correlation With Red Blood Cells and Cholesterol Crystals

Krista Nuotio, MD; Pia M. Isoviita, BM; Jani Saksi, BSc; Petra Ijäs, MD, PhD; Janne Pitkäniemi, MSc; Riitta Sonninen, BSc; Lauri Soinne, MD; Eija Saimanen, MD, PhD; Oili Salonen, MD, PhD; Petri T. Kovanen, MD, PhD; Markku Kaste, MD, PhD Perttu J. Lindsberg, MD, PhD

From the Neuroscience Program (K.N., P.M.I., J.S., P.I., R.S., P.J.L.), Biomedicum Helsinki, Finland; the Department of Neurology (K.N., P.I., L.S., M.K., P.J.L.), Helsinki University Central Hospital, Finland; the Department of Public Health (J.P.), University of Helsinki, Finland; the Department of Surgery (E.S.), South Karelia Central Hospital, Lappeenranta, Finland; the Department of Radiology (O.S.), Helsinki University Central Hospital, Finland; and the Wihuri Research Institute, Helsinki (P.T.K.), Finland.

Correspondence to Krista Nuotio, Neuroscience Program, Biomedicum Helsinki, Rm B408a1, Haartmaninkatu 8, 00290 Helsinki, Finland. E-mail Krista.Nuotio{at}helsinki.fi

Background and Purpose— Adipophilin is an adipose differentiation–related protein expressed in lipid-containing cells. Using DNA microarray analysis, we previously found the adipophilin gene (ADFP) to be overexpressed in symptomatic carotid plaques (CP). This led us to further examine the role of adipophilin in carotid atherosclerosis relative to symptom status.

Methods— Ninety-eight high-grade (>70%) CPs were obtained in carotid endarterectomy. The relative expression of ADFP mRNA was measured by quantitative real-time RT-PCR, and the relative amount of adipophilin protein was quantified with Western blotting. Detailed topographical correlations with extravasated red blood cells and extracellular cholesterol crystals were obtained by means of immunohistochemistry.

Results— The relative expression of ADFP mRNA was increased in symptomatic compared with asymptomatic CPs at both the mRNA level (1.82±0.19[SE] versus 1.25±0.15, P=0.012) and the protein level (1.04±0.23 versus 0.46±0.14, P=0.043). Adipophilin colocalized with macrophage foam cells, extravasated red blood cells (P<0.0001), and cholesterol crystals (P<0.0001), and its expression associated with macroscopic ulceration of CP (P<0.0001).

Conclusions— Intraplaque hemorrhages may contribute to intracellular lipid accumulation and consequent adipophilin expression. Because adipophilin blocks cholesterol efflux from lipid-laden cells, they may die and develop a necrotic lipid core, thereby destabilizing the plaque.

Online Data




This article has been cited by other articles:


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
B. Fan, S. Ikuyama, J.-Q. Gu, P. Wei, J.-i. Oyama, T. Inoguchi, and J. Nishimura
Oleic acid-induced ADRP expression requires both AP-1 and PPAR response elements, and is reduced by Pycnogenol through mRNA degradation in NMuLi liver cells
Am J Physiol Endocrinol Metab, July 1, 2009; 297(1): E112 - E123.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
J.-Q. Gu, S. Ikuyama, P. Wei, B. Fan, J.-i. Oyama, T. Inoguchi, and J. Nishimura
Pycnogenol, an extract from French maritime pine, suppresses Toll-like receptor 4-mediated expression of adipose differentiation-related protein in macrophages
Am J Physiol Endocrinol Metab, December 1, 2008; 295(6): E1390 - E1400.
[Abstract] [Full Text] [PDF]