• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

甲状腺激素反应性 Spot14 在人类脂肪细胞分化过程中增加,而在肥胖患者中其表达水平下调。

Thyroid hormone responsive Spot 14 increases during differentiation of human adipocytes and its expression is down-regulated in obese subjects.

机构信息

Service of Diabetes, Endocrinology and Nutrition, Institut d'Investigació Biomèdica de Girona, CIBEROBN (CB06/03/0010) and Instituto de Salud Carlos III, Girona, Spain.

出版信息

Int J Obes (Lond). 2010 Mar;34(3):487-99. doi: 10.1038/ijo.2009.263. Epub 2009 Dec 22.

DOI:10.1038/ijo.2009.263
PMID:20029374
Abstract

CONTEXT

Very limited information is available regarding the function of human thyroid hormone responsive Spot 14 (human S14, hS14) in adipogenesis and human adiposity.

OBJECTIVE

To evaluate hS14 levels during differentiation of human pre-adipocytes, in human fat depots and isolated fat cells.

DESIGN

This was a cross-sectional study.

SUBJECTS

A total of 161 omental (OM) and 87 subcutaneous (SC) adipose tissue samples obtained during elective surgical procedures from a population who varied widely in terms of obesity.

MEASUREMENTS

hS14 gene expression and protein levels during adipogenesis were assessed by RT-PCR, western blot, and using an automated confocal imaging approach.

RESULTS

hS14 gene expression levels were decreased in OM adipose tissue from overweight (-42.0%) and obese subjects (-56.5%) compared with lean subjects (P<0.05 and P<0.0001, respectively). hS14 mRNA (but not hS14-related) was inversely associated with obesity measures such as body mass index (P=0.001), percent fat mass (P=0.001), waist-to-hip ratio (P=0.020), and systolic blood pressure (P=0.031). hS14 gene expression and protein levels were up-regulated at the early stages of differentiation of human pre-adipocytes as well as for 3T3-L1 cells. That observation was most prominent in those individual cells exhibiting the more marked differentiation features. hS14 gene expression levels increased by approximately 45 000-fold in mature adipocytes. Increased hS14 levels were also found in stromal-vascular cells/pre-adipocytes (3.8-fold, P<0.05) and in adipose tissue samples (1.9-fold, P<0.0001) from SC compared with OM fat depots.

CONCLUSIONS

These results suggest that hS14 is involved in human adipogenesis, but inversely related to obesity and OM fat accumulation.

摘要

背景

关于人类甲状腺激素反应性 Spot 14(人类 S14,hS14)在脂肪生成和人类肥胖中的功能,信息非常有限。

目的

评估人前脂肪细胞分化过程中、人体脂肪组织和分离脂肪细胞中 hS14 的水平。

设计

这是一项横断面研究。

受试者

从不同肥胖程度的人群接受择期手术时获得的总共 161 个网膜(OM)和 87 个皮下(SC)脂肪组织样本。

测量

通过 RT-PCR、western blot 和自动共聚焦成像方法评估脂肪生成过程中 hS14 基因表达和蛋白水平。

结果

与瘦受试者相比,超重(-42.0%)和肥胖(-56.5%)受试者的 OM 脂肪组织中 hS14 基因表达水平降低(P<0.05 和 P<0.0001)。hS14 mRNA(而非 hS14 相关)与肥胖指标如体重指数(P=0.001)、体脂肪百分比(P=0.001)、腰臀比(P=0.020)和收缩压(P=0.031)呈负相关。人前脂肪细胞的早期分化以及 3T3-L1 细胞中 hS14 基因表达和蛋白水平上调。在表现出更明显分化特征的个别细胞中,这种观察最为明显。成熟脂肪细胞中 hS14 基因表达水平增加了约 45000 倍。与 OM 脂肪组织相比,SC 中的基质血管细胞/前脂肪细胞(3.8 倍,P<0.05)和脂肪组织样本(1.9 倍,P<0.0001)中也发现 hS14 水平升高。

结论

这些结果表明 hS14 参与了人类脂肪生成,但与肥胖和 OM 脂肪堆积呈负相关。

相似文献

1
Thyroid hormone responsive Spot 14 increases during differentiation of human adipocytes and its expression is down-regulated in obese subjects.甲状腺激素反应性 Spot14 在人类脂肪细胞分化过程中增加,而在肥胖患者中其表达水平下调。
Int J Obes (Lond). 2010 Mar;34(3):487-99. doi: 10.1038/ijo.2009.263. Epub 2009 Dec 22.
2
Subcutaneous fat shows higher thyroid hormone receptor-alpha1 gene expression than omental fat.皮下脂肪的甲状腺激素受体-α1 基因表达高于网膜脂肪。
Obesity (Silver Spring). 2009 Dec;17(12):2134-41. doi: 10.1038/oby.2009.110. Epub 2009 Apr 9.
3
Type I iodothyronine 5'-deiodinase mRNA and activity is increased in adipose tissue of obese subjects.肥胖症患者脂肪组织中的 I 型碘甲状腺原氨酸 5'-脱碘酶 mRNA 和活性增加。
Int J Obes (Lond). 2012 Feb;36(2):320-4. doi: 10.1038/ijo.2011.101. Epub 2011 May 24.
4
SH21B, an anti-obesity herbal composition, inhibits fat accumulation in 3T3-L1 adipocytes and high fat diet-induced obese mice through the modulation of the adipogenesis pathway.SH21B,一种减肥草药组合物,通过调节脂肪生成途径抑制 3T3-L1 脂肪细胞和高脂肪饮食诱导肥胖小鼠的脂肪积累。
J Ethnopharmacol. 2010 Feb 17;127(3):709-17. doi: 10.1016/j.jep.2009.12.002. Epub 2009 Dec 4.
5
The gene expression of the main lipogenic enzymes is downregulated in visceral adipose tissue of obese subjects.肥胖患者内脏脂肪组织中主要脂肪生成酶的基因表达下调。
Obesity (Silver Spring). 2010 Jan;18(1):13-20. doi: 10.1038/oby.2009.202. Epub 2009 Jun 18.
6
Human growth hormone receptor (GHR) expression in obesity: I. GHR mRNA expression in omental and subcutaneous adipose tissues of obese women.肥胖人群中生长激素受体(GHR)的表达:I. 肥胖女性网膜和皮下脂肪组织中 GHR mRNA 的表达。
Int J Obes (Lond). 2011 Dec;35(12):1511-9. doi: 10.1038/ijo.2011.23. Epub 2011 Mar 8.
7
The fatty acid transporter FAT/CD36 is upregulated in subcutaneous and visceral adipose tissues in human obesity and type 2 diabetes.脂肪酸转运蛋白FAT/CD36在人类肥胖症和2型糖尿病患者的皮下及内脏脂肪组织中表达上调。
Int J Obes (Lond). 2006 Jun;30(6):877-83. doi: 10.1038/sj.ijo.0803212.
8
Amyloid precursor protein expression is upregulated in adipocytes in obesity.肥胖状态下,脂肪细胞中淀粉样前体蛋白的表达上调。
Obesity (Silver Spring). 2008 Jul;16(7):1493-500. doi: 10.1038/oby.2008.267. Epub 2008 May 15.
9
Endothelin-1 stimulates human adipocyte lipolysis through the ET A receptor.内皮素-1通过ET A受体刺激人脂肪细胞的脂肪分解。
Int J Obes (Lond). 2009 Jan;33(1):67-74. doi: 10.1038/ijo.2008.212. Epub 2008 Nov 4.
10
Pathways of adipose tissue androgen metabolism in women: depot differences and modulation by adipogenesis.女性脂肪组织雄激素代谢途径:储存部位差异及脂肪生成的调节作用
Am J Physiol Endocrinol Metab. 2009 Feb;296(2):E244-55. doi: 10.1152/ajpendo.00039.2008. Epub 2008 Nov 4.

引用本文的文献

1
Spot-14 and its paralog Spot-14R regulate expression of metabolic and thermogenic pathway genes in murine brown and beige adipocytes.斑点蛋白14及其旁系同源物斑点蛋白14R调节小鼠棕色和米色脂肪细胞中代谢和产热途径基因的表达。
FEBS Lett. 2025 Jun;599(12):1760-1780. doi: 10.1002/1873-3468.70052. Epub 2025 May 2.
2
Insulin-inducible THRSP maintains mitochondrial function and regulates sphingolipid metabolism in human adipocytes.胰岛素诱导的 THRSP 维持人脂肪细胞中线粒体功能并调节神经酰胺代谢。
Mol Med. 2022 Jun 17;28(1):68. doi: 10.1186/s10020-022-00496-3.
3
A Nine-Strain Bacterial Consortium Improves Portal Hypertension and Insulin Signaling and Delays NAFLD Progression In Vivo.
一种九菌株细菌联合体可改善门静脉高压和胰岛素信号传导,并延缓非酒精性脂肪性肝病在体内的进展。
Biomedicines. 2022 May 20;10(5):1191. doi: 10.3390/biomedicines10051191.
4
Genetic regulation and variation of expression of miRNA and mRNA transcripts in fetal muscle tissue in the context of sex, dam and variable fetal weight.miRNA 和 mRNA 转录本在胎儿肌肉组织中的遗传调控和表达变化及其与性别、母体和胎儿体重变化的关系。
Biol Sex Differ. 2022 May 12;13(1):24. doi: 10.1186/s13293-022-00433-3.
5
Bone Marrow Adiposity in Models of Radiation- and Aging-Related Bone Loss Is Dependent on Cellular Senescence.辐射和衰老相关的骨丢失模型中的骨髓脂肪含量依赖于细胞衰老。
J Bone Miner Res. 2022 May;37(5):997-1011. doi: 10.1002/jbmr.4537. Epub 2022 Mar 29.
6
Elevated serum S14 levels are associated with more severe liver steatosis by ultrasonography.血清 S14 水平升高与超声检查显示的更严重的肝脂肪变性相关。
Sci Rep. 2021 Dec 17;11(1):24181. doi: 10.1038/s41598-021-03279-8.
7
CLARITY-BPA: Bisphenol A or Propylthiouracil on Thyroid Function and Effects in the Developing Male and Female Rat Brain.CLARITY-BPA:双酚 A 或丙硫氧嘧啶对雄性和雌性幼鼠大脑甲状腺功能和影响的研究。
Endocrinology. 2019 Aug 1;160(8):1771-1785. doi: 10.1210/en.2019-00121.
8
Genetic Regulation of Liver Metabolites and Transcripts Linking to Biochemical-Clinical Parameters.与生化临床参数相关的肝脏代谢物和转录本的基因调控
Front Genet. 2019 Apr 17;10:348. doi: 10.3389/fgene.2019.00348. eCollection 2019.
9
Proposal of a study protocol of a preliminary double-blind randomized controlled trial. Verifying effects of selenium supplementation on selenoprotein p and s genes expression in protein and mRNA levels in subjects with coronary artery disease: selenegene.一项初步双盲随机对照试验研究方案的提议。验证补充硒对冠心病患者蛋白质和mRNA水平上硒蛋白p和s基因表达的影响:selenegene研究。
Acta Biomed. 2019 Jan 22;90(1):44-50. doi: 10.23750/abm.v90i1.6167.
10
The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome.新型脂肪生成蛋白 Spot 14 的血清水平在代谢综合征中降低。
PLoS One. 2019 Feb 14;14(2):e0212341. doi: 10.1371/journal.pone.0212341. eCollection 2019.