27-Hydroxycholesterol Promotes Adiposity and Mimics Adipogenic Diet-Induced Inflammatory Signaling

被引:20
作者
Asghari, Arvand [1 ]
Ishikawa, Tomonori [2 ]
Hiramitsu, Shiro [1 ]
Lee, Wan-Ru [2 ]
Umetani, Junko [2 ]
Bui, Linh [1 ]
Korach, Kenneth S. [3 ]
Umetani, Michihisa [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Ctr Nucl Receptors & Cell Signaling, Houston, TX 77204 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Pediat, Div Pulm & Vasc Biol, Dallas, TX 75390 USA
[3] NIEHS, Reprod & Dev Biol Lab, POB 12233, Res Triangle Pk, NC 27709 USA
基金
美国国家卫生研究院;
关键词
CHOLESTEROL-METABOLISM; ESTROGEN; TISSUE; OXYSTEROLS; RECEPTORS; STRINGTIE; GENE;
D O I
10.1210/en.2019-00349
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
27-Hydroxycholesterol (27HC) is an abundant cholesterol metabolite and has detrimental effects on the cardiovascular system, whereas its impact on adiposity is not well known. In this study, we found that elevations in 27HC cause increased body weight gain in mice fed a high-fat/high-cholesterol diet in an estrogen receptor alpha-dependent manner. Regardless of diet type, body fat mass was increased by 27HC without changes in food intake or fat absorption. 27HC did not alter energy expenditure in mice fed a normal chow diet and increased visceral white adipose mass by inducing hyperplasia but not hypertrophy. Although 27HC did not augment adipocyte terminal differentiation, it increased the adipose cell population that differentiates to mature adipocytes. RNA sequencing analysis revealed that 27HC treatment of mice fed a normal chow diet induces inflammatory gene sets similar to those seen after high-fat/high-cholesterol diet feeding, whereas there was no overlap in inflammatory gene expression among any other 27HC administration/diet change combination. Histological analysis showed that 27HC treatment increased the number of total and M1-type macrophages in white adipose tissues. Thus, 27HC promotes adiposity by directly affecting white adipose tissues and by increasing adipose inflammatory responses. Lowering serum 27HC levels may lead to an approach targeting cholesterol to prevent diet-induced obesity.
引用
收藏
页码:2485 / 2494
页数:10
相关论文
共 41 条
[1]   Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation [J].
Bernard, Valerie ;
Kherra, Sakina ;
Francou, Bruno ;
Fagart, Jerome ;
Viengchareun, Say ;
Guechot, Jerome ;
Ladjouze, Asmahane ;
Guiochon-Mantel, Anne ;
Korach, Kenneth S. ;
Binart, Nadine ;
Lombes, Marc ;
Christin-Maitre, Sophie .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2017, 102 (01) :93-99
[2]   Oxysterols and atherosclerosis [J].
Brown, AJ ;
Jessup, W .
ATHEROSCLEROSIS, 1999, 142 (01) :1-28
[3]   Lipoprotein distribution and biological variation of 24S-and 27-hydroxycholesterol in healthy volunteers [J].
Burkard, Ines ;
von Eckardstein, Arnold ;
Waeber, Gerard ;
Vollenweider, Peter ;
Rentsch, Katharina M. .
ATHEROSCLEROSIS, 2007, 194 (01) :71-78
[4]   Effect of testosterone and estradiol in a man with aromatase deficiency [J].
Carani, C ;
Qin, K ;
Simoni, M ;
FaustiniFustini, M ;
Serpente, S ;
Boyd, J ;
Korach, KS ;
Simpson, ER .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (02) :91-95
[5]   The emergence of the metabolic syndrome with menopause [J].
Carr, MC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (06) :2404-2411
[6]   Relationships between Rodent white Adipose Fat Pads and Human white Adipose Fat Depots [J].
Chusyd, Daniella E. ;
Wang, Donghai ;
Huffman, Derek M. ;
Nagy, Tim R. .
FRONTIERS IN NUTRITION, 2016, 3
[7]   Role of estrogens in adipocyte development and function [J].
Cooke, PS ;
Naaz, A .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 229 (11) :1127-1135
[8]   The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis [J].
Crewe, Clair ;
An, Yu Aaron ;
Scherer, Philipp E. .
JOURNAL OF CLINICAL INVESTIGATION, 2017, 127 (01) :74-82
[9]   The sexually dimorphic role of adipose and adipocyte estrogen receptors in modulating adipose tissue expansion, inflammation, and fibrosis [J].
Davis, Kathryn E. ;
Neinast, Michael D. ;
Sun, Kai ;
Skiles, William M. ;
Bills, Jessica D. ;
Zehr, Jordan A. ;
Zeve, Daniel ;
Hahner, Lisa D. ;
Cox, Derek W. ;
Gent, Lana M. ;
Xu, Yong ;
Wang, Zhao V. ;
Khan, Sohaib A. ;
Clegg, Deborah J. .
MOLECULAR METABOLISM, 2013, 2 (03) :227-242
[10]   27-hydroxycholesterol is an endogenous selective estrogen receptor modulator [J].
DuSell, Carolyn D. ;
Umetani, Michihisa ;
Shaul, Philip W. ;
Mangelsdorf, David J. ;
McDonnell, Donald P. .
MOLECULAR ENDOCRINOLOGY, 2008, 22 (01) :65-77