TY - JOUR
T1 - RNA binding protein HuR regulates the expression of ABCA1
AU - Ramírez, Cristina M.
AU - Lin, Chin Sheng
AU - Abdelmohsen, Kotb
AU - Goedeke, Leigh
AU - Yoon, Je Hyun
AU - Madrigal-Matute, Julio
AU - Martin-Ventura, Jose L.
AU - Vo, Dat T.
AU - Uren, Philip J.
AU - Penalva, Luiz O.
AU - Gorospe, Myriam
AU - Fernández-Hernando, Carlos
PY - 2014/6
Y1 - 2014/6
N2 - ABCA1 is a major regulator of cellular cholesterol effl ux and plasma HDL biogenesis. Even though the transcriptional activation of ABCA1 is well established, the posttranscriptional regulation of ABCA1 expression is poorly understood. Here, we investigate the potential contribution of the RNA binding protein (RBP) human antigen R (HuR) on the posttranscriptional regulation of ABCA1 expression. RNA immunoprecipitation assays demonstrate a direct interaction between HuR and ABCA1 mRNA. We found that HuR binds to the 3 Œ untranslated region of ABCA1 and increases ABCA1 translation, while HuR silencing reduces ABCA1 expression and cholesterol effl ux to ApoA1 in human hepatic (Huh-7) and monocytic (THP-1) cells. Interestingly, cellular cholesterol levels regulate the expression, intracellular localization, and interaction between HuR and ABCA1 mRNA. Finally, we found that HuR expression was signifi cantly increased in macrophages from human atherosclerotic plaques, suggesting an important role for this RBP in controlling macrophage cholesterol metabolism in vivo. In summary, we have identifi ed HuR as a novel posttranscriptional regulator of ABCA1 expression and cellular cholesterol homeostasis, thereby opening new avenues for increasing cholesterol effl ux from atherosclerotic foam macrophages and raising circulating HDL cholesterol levels.
AB - ABCA1 is a major regulator of cellular cholesterol effl ux and plasma HDL biogenesis. Even though the transcriptional activation of ABCA1 is well established, the posttranscriptional regulation of ABCA1 expression is poorly understood. Here, we investigate the potential contribution of the RNA binding protein (RBP) human antigen R (HuR) on the posttranscriptional regulation of ABCA1 expression. RNA immunoprecipitation assays demonstrate a direct interaction between HuR and ABCA1 mRNA. We found that HuR binds to the 3 Œ untranslated region of ABCA1 and increases ABCA1 translation, while HuR silencing reduces ABCA1 expression and cholesterol effl ux to ApoA1 in human hepatic (Huh-7) and monocytic (THP-1) cells. Interestingly, cellular cholesterol levels regulate the expression, intracellular localization, and interaction between HuR and ABCA1 mRNA. Finally, we found that HuR expression was signifi cantly increased in macrophages from human atherosclerotic plaques, suggesting an important role for this RBP in controlling macrophage cholesterol metabolism in vivo. In summary, we have identifi ed HuR as a novel posttranscriptional regulator of ABCA1 expression and cellular cholesterol homeostasis, thereby opening new avenues for increasing cholesterol effl ux from atherosclerotic foam macrophages and raising circulating HDL cholesterol levels.
KW - ATP binding cassette transporter A1
KW - Cholesterol efflux
KW - Human antigen R
KW - Lipid homeostasis
KW - Posttranscriptional regulation
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U2 - 10.1194/jlr.M044925
DO - 10.1194/jlr.M044925
M3 - Article
C2 - 24729624
AN - SCOPUS:84901659790
SN - 0022-2275
VL - 55
SP - 1066
EP - 1076
JO - Journal of Lipid Research
JF - Journal of Lipid Research
IS - 6
ER -