دورية أكاديمية
Retinoic Acid Isomers Facilitate Apolipoprotein E Production and Lipidation in Astrocytes through the Retinoid X Receptor/Retinoic Acid Receptor Pathway
| العنوان: | Retinoic Acid Isomers Facilitate Apolipoprotein E Production and Lipidation in Astrocytes through the Retinoid X Receptor/Retinoic Acid Receptor Pathway |
|---|---|
| المؤلفون: | Zhao, Jing, Fu, Yuan, Liu, Chia-Chen, Shinohara, Mitsuru, Nielsen, Henrietta M., Dong, Qiang, Kanekiyo, Takahisa, Bu, Guojun, 卜国军 |
| المصدر: | http://dx.doi.org/10.1074/jbc.M113.526095Test. |
| بيانات النشر: | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC |
| سنة النشر: | 2014 |
| المجموعة: | Xiamen University Institutional Repository |
| مصطلحات موضوعية: | AD MOUSE MODELS, AMYLOID-ASSOCIATED PROTEINS, CENTRAL-NERVOUS-SYSTEM, UNION-OF-PHARMACOLOGY, ALZHEIMERS-DISEASE, REVERSE DEFICITS, CEREBROSPINAL-FLUID, CHOLESTEROL EFFLUX, PRECURSOR PROTEIN, MEMORY DEFICITS |
| الوصف: | National Institutes of Health [R01AG046205, R01AG035355, R01AG027924, P01AG030128, P01NS074969]; Alzheimer's Drug Discovery Foundation; Alzheimer's Association New Investigator Research Grant; Mayo Clinic Center for Regenerative Medicine Career Development Award ; Background: Apolipoprotein E (apoE) isoforms influence the risk for Alzheimer disease (AD). Results: All-trans-retinoic acid (RA), 9-cis-RA, and 13-cis-RA were identified as compounds that increase apoE expression and lipidation in astrocytes. Conclusion: RA isomers are effective modulators of apoE production through the retinoid X receptor (RXR) and RA receptor (RAR). Significance: RXR/RAR agonists can be explored for AD therapy. Apolipoprotein E (apoE) is the major cholesterol transport protein in the brain. Among the three human APOE alleles (APOE2, APOE3, and APOE4), APOE4 is the strongest genetic risk factor for late-onset Alzheimer disease (AD). The accumulation of amyloid- (A) is a central event in AD pathogenesis. Increasing evidence demonstrates that apoE isoforms differentially regulate AD-related pathways through both A-dependent and -independent mechanisms; therefore, modulating apoE secretion, lipidation, and function might be an attractive approach for AD therapy. We performed a drug screen for compounds that modulate apoE production in immortalized astrocytes derived from apoE3-targeted replacement mice. Here, we report that retinoic acid (RA) isomers, including all-trans-RA, 9-cis-RA, and 13-cis-RA, significantly increase apoE secretion to approximate to 4-fold of control through retinoid X receptor (RXR) and RA receptor. These effects on modulating apoE are comparable with the effects recently reported for the RXR agonist bexarotene. Furthermore, all of these compounds increased the expression of the cholesterol transporter ABCA1 and ABCG1 levels and decreased cellular uptake of A in an apoE-dependent manner. Both bexarotene and 9-cis-RA promote the lipidation status of apoE, in which 9-cis-RA promotes a stronger effect and exhibits ... |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | JOURNAL OF BIOLOGICAL CHEMISTRY, 2014,289(16):11282-11292; WOS:000334638500031; http://dspace.xmu.edu.cn/handle/2288/93625Test |
| الإتاحة: | https://doi.org/10.1074/jbc.M113.526095Test http://dspace.xmu.edu.cn/handle/2288/93625Test |
| رقم الانضمام: | edsbas.953CE27A |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |