• 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

衰老、脂肪组织来源和前脂肪细胞基因表达。

Aging, depot origin, and preadipocyte gene expression.

机构信息

Department of Medicine, Boston University, Massachusetts, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2010 Mar;65(3):242-51. doi: 10.1093/gerona/glp213. Epub 2010 Jan 27.

DOI:10.1093/gerona/glp213
PMID:20106964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904595/
Abstract

Fat distribution changes with aging. Inherent changes in fat cell progenitors may contribute because fat cells turn over throughout life. To define mechanisms, gene expression was profiled in preadipocytes cultured from epididymal and perirenal depots of young and old rats. 8.4% of probe sets differed significantly between depots, particularly developmental genes. Only 0.02% differed with aging, despite using less stringent criteria than for comparing depots. Twenty-five genes selected based on fold change with aging were analyzed in preadipocytes from additional young, middle-aged, and old animals by polymerase chain reaction. Thirteen changed significantly with aging, 13 among depots, and 9 with both. Genes involved in inflammation, stress, and differentiation changed with aging, as occurs in fat tissue. Age-related changes were greater in perirenal than epididymal preadipocytes, consistent with larger declines in replication and adipogenesis in perirenal preadipocytes. Thus, age-related changes in preadipocyte gene expression differ among depots, potentially contributing to fat redistribution and dysfunction.

摘要

脂肪分布随年龄而变化。脂肪细胞祖细胞的固有变化可能是造成这种变化的原因,因为脂肪细胞在整个生命周期中都会更新。为了明确机制,我们对从小鼠附睾和肾周脂肪组织培养的前体脂肪细胞中的基因表达进行了分析。8.4%的探针在不同部位之间差异显著,特别是发育基因。尽管与比较不同部位相比,使用的标准不那么严格,但只有 0.02%的基因随年龄而变化。根据与衰老相关的倍数变化,从额外的年轻、中年和老年动物的前体脂肪细胞中选择了 25 个基因进行聚合酶链反应分析。其中 13 个与衰老相关,13 个与部位相关,9 个与两者都相关。与炎症、应激和分化相关的基因随衰老而变化,就像在脂肪组织中一样。肾周前体脂肪细胞的衰老相关变化大于附睾前体脂肪细胞,这与肾周前体脂肪细胞的复制和脂肪生成能力下降更大有关。因此,前体脂肪细胞基因表达的衰老相关变化在不同部位之间存在差异,这可能是导致脂肪重新分布和功能障碍的原因之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/95e77aaf2a46/geronaglp213f04_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/6e0fec9cd7ce/geronaglp213f01_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/cde76e18b5b2/geronaglp213f02_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/f1596f79dfad/geronaglp213f03_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/95e77aaf2a46/geronaglp213f04_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/6e0fec9cd7ce/geronaglp213f01_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/cde76e18b5b2/geronaglp213f02_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/f1596f79dfad/geronaglp213f03_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc39/2904595/95e77aaf2a46/geronaglp213f04_ht.jpg

相似文献

1
Aging, depot origin, and preadipocyte gene expression.衰老、脂肪组织来源和前脂肪细胞基因表达。
J Gerontol A Biol Sci Med Sci. 2010 Mar;65(3):242-51. doi: 10.1093/gerona/glp213. Epub 2010 Jan 27.
2
Thiazolidinedione exposure increases the expression of uncoupling protein 1 in cultured human preadipocytes.噻唑烷二酮类药物暴露可增加培养的人前脂肪细胞中解偶联蛋白1的表达。
Diabetes. 1998 Jan;47(1):138-41. doi: 10.2337/diab.47.1.138.
3
Increased TNFalpha and CCAAT/enhancer-binding protein homologous protein with aging predispose preadipocytes to resist adipogenesis.随着衰老,肿瘤坏死因子α(TNFα)和CCAAT/增强子结合蛋白同源蛋白增加,使前脂肪细胞易发生脂肪生成抵抗。
Am J Physiol Endocrinol Metab. 2007 Dec;293(6):E1810-9. doi: 10.1152/ajpendo.00295.2007. Epub 2007 Oct 2.
4
Fat depot origin affects fatty acid handling in cultured rat and human preadipocytes.脂肪储存部位的来源会影响培养的大鼠和人类前脂肪细胞中脂肪酸的处理。
Am J Physiol Endocrinol Metab. 2001 Feb;280(2):E238-47. doi: 10.1152/ajpendo.2001.280.2.E238.
5
Effects of age and anatomic site on preadipocyte number in rat fat depots.年龄和解剖部位对大鼠脂肪库中前脂肪细胞数量的影响。
J Gerontol. 1994 Jan;49(1):B31-5. doi: 10.1093/geronj/49.1.b31.
6
Aging and regional differences in fat cell progenitors - a mini-review.脂肪细胞祖细胞的衰老与区域差异——综述
Gerontology. 2011;57(1):66-75. doi: 10.1159/000279755. Epub 2010 Jan 29.
7
Effects of fat depot site on differentiation-dependent gene expression in rat preadipocytes.脂肪储存部位对大鼠前脂肪细胞中分化相关基因表达的影响。
Int J Obes Relat Metab Disord. 1996 Mar;20 Suppl 3:S102-7.
8
Aging in adipocytes: potential impact of inherent, depot-specific mechanisms.脂肪细胞衰老:内在的、特定部位机制的潜在影响。
Exp Gerontol. 2007 Jun;42(6):463-71. doi: 10.1016/j.exger.2007.03.003. Epub 2007 Mar 25.
9
Aging results in paradoxical susceptibility of fat cell progenitors to lipotoxicity.衰老导致脂肪细胞祖细胞对脂毒性产生矛盾的易感性。
Am J Physiol Endocrinol Metab. 2007 Apr;292(4):E1041-51. doi: 10.1152/ajpendo.00557.2006. Epub 2006 Dec 5.
10
Modulation of rat preadipocyte adipose conversion by androgenic status: involvement of C/EBPs transcription factors.雄激素状态对大鼠前脂肪细胞脂肪转化的调节作用:C/EBPs转录因子的参与
J Endocrinol. 1999 Apr;161(1):89-97. doi: 10.1677/joe.0.1610089.

引用本文的文献

1
Pharmacological inhibition of G protein-coupled receptor kinase 5 decreases high-fat diet-induced hepatic steatosis in mice.G蛋白偶联受体激酶5的药理学抑制作用可减轻高脂饮食诱导的小鼠肝脏脂肪变性。
bioRxiv. 2025 Jun 28:2025.06.25.661655. doi: 10.1101/2025.06.25.661655.
2
The Interplay Between Obesity and Type 2 Diabetes: Common Pathophysiological Mechanisms Contributing to Telomere Shortening.肥胖与2型糖尿病之间的相互作用:导致端粒缩短的共同病理生理机制
Life (Basel). 2025 May 28;15(6):873. doi: 10.3390/life15060873.
3
Enhancing adipose tissue functionality in obesity: senotherapeutics, autophagy and cellular senescence as a target.

本文引用的文献

1
Inflammation and impaired adipogenesis in hypertrophic obesity in man.人类肥胖症中肥大与脂肪生成受损相关的炎症反应。
Am J Physiol Endocrinol Metab. 2009 Nov;297(5):E999-E1003. doi: 10.1152/ajpendo.00377.2009. Epub 2009 Jul 21.
2
Differential expression of cytokines in subcutaneous and marrow fat of aging C57BL/6J mice.衰老 C57BL/6J 小鼠皮下和骨髓脂肪中细胞因子的差异表达。
Exp Gerontol. 2009 Sep;44(9):613-8. doi: 10.1016/j.exger.2009.05.009. Epub 2009 Jun 6.
3
Dynamics of fat cell turnover in humans.人类脂肪细胞更新的动态变化
增强肥胖症患者的脂肪组织功能:衰老治疗学、自噬和细胞衰老作为靶点。
Biol Res. 2024 Aug 8;57(1):51. doi: 10.1186/s40659-024-00531-z.
4
Aging and homeostasis of the hypodermis in the age-related deterioration of skin function.随着皮肤功能的衰老相关性下降,皮下组织的衰老和内稳态。
Cell Death Dis. 2024 Jun 24;15(6):443. doi: 10.1038/s41419-024-06818-z.
5
Caloric restriction mitigates age-associated senescence characteristics in subcutaneous adipose tissue-derived stem cells.热量限制减轻了来源于皮下脂肪组织的干细胞的与年龄相关的衰老特征。
Aging (Albany NY). 2024 May 9;16(9):7535-7552. doi: 10.18632/aging.205812.
6
From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and Inflammation.从太阳到细胞:透过维生素D与炎症的视角审视肥胖症
Metabolites. 2023 Dec 20;14(1):4. doi: 10.3390/metabo14010004.
7
Insight into the function of tetranectin in human diseases: A review and prospects for tetranectin-targeted disease treatment.纤连蛋白在人类疾病中的功能洞察:纤连蛋白靶向疾病治疗的综述与展望
Heliyon. 2023 Dec 10;10(1):e23512. doi: 10.1016/j.heliyon.2023.e23512. eCollection 2024 Jan 15.
8
Nicotinamide Riboside Improves Stemness of Human Adipose-Derived Stem Cells and Inhibits Terminal Adipocyte Differentiation.烟酰胺核糖可改善人脂肪干细胞的干性并抑制脂肪细胞终末分化。
Pharmaceuticals (Basel). 2023 Aug 10;16(8):1134. doi: 10.3390/ph16081134.
9
Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs.毛发根部基因表达谱的改变突出了钙信号传导和脂质代谢途径与曼加利察猪卷曲毛发生成及维持的关联。
Front Genet. 2023 Jun 7;14:1184015. doi: 10.3389/fgene.2023.1184015. eCollection 2023.
10
Hydroxylation markedly alters how the polychlorinated biphenyl (PCB) congener, PCB52, affects gene expression in human preadipocytes.羟基化显著改变了多氯联苯(PCB)同系物 PCB52 对人前脂肪细胞基因表达的影响。
Toxicol In Vitro. 2023 Jun;89:105568. doi: 10.1016/j.tiv.2023.105568. Epub 2023 Feb 15.
Nature. 2008 Jun 5;453(7196):783-7. doi: 10.1038/nature06902. Epub 2008 May 4.
4
Characterization of transplanted green fluorescent protein+ bone marrow cells into adipose tissue.移植到脂肪组织中的绿色荧光蛋白阳性骨髓细胞的特性分析。
Stem Cells. 2008 Feb;26(2):330-8. doi: 10.1634/stemcells.2007-0567. Epub 2007 Nov 1.
5
Increased TNFalpha and CCAAT/enhancer-binding protein homologous protein with aging predispose preadipocytes to resist adipogenesis.随着衰老,肿瘤坏死因子α(TNFα)和CCAAT/增强子结合蛋白同源蛋白增加,使前脂肪细胞易发生脂肪生成抵抗。
Am J Physiol Endocrinol Metab. 2007 Dec;293(6):E1810-9. doi: 10.1152/ajpendo.00295.2007. Epub 2007 Oct 2.
6
Transcriptional response to aging and caloric restriction in heart and adipose tissue.心脏和脂肪组织对衰老及热量限制的转录反应。
Aging Cell. 2007 Oct;6(5):673-88. doi: 10.1111/j.1474-9726.2007.00319.x.
7
Aging in adipocytes: potential impact of inherent, depot-specific mechanisms.脂肪细胞衰老:内在的、特定部位机制的潜在影响。
Exp Gerontol. 2007 Jun;42(6):463-71. doi: 10.1016/j.exger.2007.03.003. Epub 2007 Mar 25.
8
Rosiglitazone promotes development of a novel adipocyte population from bone marrow-derived circulating progenitor cells.罗格列酮促进骨髓来源的循环祖细胞形成一种新型脂肪细胞群体。
J Clin Invest. 2006 Dec;116(12):3220-8. doi: 10.1172/JCI28510.
9
Prevention of high-fat diet-induced adipose tissue remodeling in obese diabetic mice by n-3 polyunsaturated fatty acids.n-3多不饱和脂肪酸预防肥胖糖尿病小鼠高脂饮食诱导的脂肪组织重塑
Int J Obes (Lond). 2007 Jun;31(6):1004-13. doi: 10.1038/sj.ijo.0803511. Epub 2006 Nov 28.
10
Differential expression of matrix metalloproteinase 3 (MMP3) in preadipocytes/stromal vascular cells from nonobese nondiabetic versus obese nondiabetic Pima Indians.非肥胖非糖尿病与肥胖非糖尿病皮马印第安人前脂肪细胞/基质血管细胞中基质金属蛋白酶3(MMP3)的差异表达
Diabetes. 2006 Nov;55(11):3160-5. doi: 10.2337/db06-0373.