4.8 Article Retracted Publication

被撤回的出版物: Annexin 2-caveolin 1 complex is a target of ezetimibe and regulates intestinal cholesterol transport (Retracted article. See vol. 110, pg. 797, 2013)

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.0400441101

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  1. NHLBI NIH HHS [R01 HL058475, R01 HL064056, HL64056, HL58475, HL62844] Funding Source: Medline
  2. NIDDK NIH HHS [DK60369, R01 DK060369] Funding Source: Medline
  3. NIGMS NIH HHS [GM63904, R56 GM063904, R01 GM063904-01, R01 GM063904] Funding Source: Medline

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Modulation of cholesterol absorption in the intestine, the primary site of dietary cholesterol uptake in humans, can have profound clinical implications. We have undertaken a reverse genetic approach by disrupting putative cholesterol processing genes in zebrafish larvae by using morpholino (MO) antisense oligonucleoticles. By using targeted MO injections and immunoprecipitation (IP) experiments coupled with mass spectrometry, we determined that annexin (ANX)2 complexes with caveolin (CAV)1 in the zebrafish and mouse intestine. The complex is heat stable and unaffected by SDS or reducing conditions. MO targeting of anx2b or cav1, which are both strongly expressed in the larval and adult zebrafish intestinal epithelium, prevents formation of the protein heterocomplex. Furthermore, anx2b MO injection prevents processing of a fluorescent cholesterol reporter and results in reduced sterol mass. Pharmacological treatment of mice with ezetimibe disrupts the heterocomplex in only hypercholesterolemic animals. These data suggest that ANX2 and CAV1 are components of an intestinal sterol transport complex.

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