• 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

Syndecan-1 表达降低的小鼠的代谢和行为参数。

Metabolic and behavioral parameters of mice with reduced expression of Syndecan-1.

机构信息

Central Unit for Animal Research and Animal Welfare Affairs (ZETT) of the Heinrich-Heine-University of Düsseldorf, Düsseldorf, Germany.

Düsseldorf University Hospital, Department of OB/GYN and REI (UniKiD), Düsseldorf, Germany.

出版信息

PLoS One. 2019 Jul 12;14(7):e0219604. doi: 10.1371/journal.pone.0219604. eCollection 2019.

DOI:10.1371/journal.pone.0219604
PMID:31299063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6625734/
Abstract

Energy balance is essential for all species. Ligand-receptor interactions mediate processes that regulate body activities like reproduction and metabolism based on the energy status. Such receptors are the heparan sulfate proteoglycans and specifically the family of syndecans. Therefore we investigated the differences of metabolic parameters of heterozygous Syndecan 1 mice (Sdc1+/-) with reduced expression of Sdc1 and the corresponding wild type mice. Sdc1+/- mice have a reduced body weight although they show increased leptin and decreased corticosterone levels. Furthermore, their food and water intake is increased. This is accompanied with less adipose tissue, smaller adipocytes and thus an increased density of adipocytes. For the detailed analysis of the metabolism the automated PhenoMaster system has been used, which allowed continuous and undisturbed recording of food and water intake, energy expenditure and movement. The reason for the lower body weight was the higher energy expenditure of these animals compared to controls. Additionally, female Sdc1+/- mice showed an increased locomotor activity. Referring to organs, the intestine in Sdc1+/- mice was heavier and longer, but no differences at the cellular level could be observed. These findings were independent of normal mating or vice versa embryo transfers of Sdc1+/- and wild type embryos in recipient females of the other genotype. Herein we showed that the reduced expression of Sdc1 led to an altered metabolism on fetal as well as on maternal side, which may play a role in the growth restriction observed in human pregnancy pathologies and in mice lacking Sdc1.

摘要

能量平衡对所有物种都是至关重要的。配体-受体相互作用介导了根据能量状态调节身体活动的过程,如繁殖和代谢。这些受体是硫酸乙酰肝素蛋白聚糖,特别是 syndecan 家族。因此,我们研究了表达减少的 Syndecan 1 杂合子(Sdc1+/-)小鼠与相应野生型小鼠代谢参数的差异。尽管 Sdc1+/- 小鼠的瘦素水平升高,皮质酮水平降低,但它们的体重却减轻了。此外,它们的食物和水摄入量增加。这伴随着更少的脂肪组织,更小的脂肪细胞,因此脂肪细胞的密度增加。为了详细分析代谢情况,使用了自动化 PhenoMaster 系统,该系统允许连续和不受干扰地记录食物和水的摄入量、能量消耗和运动。这些动物的体重较低是由于它们的能量消耗高于对照动物。此外,Sdc1+/- 雌性小鼠的运动活性增加。就器官而言,Sdc1+/- 小鼠的肠道更重、更长,但在细胞水平上没有观察到差异。这些发现与正常交配无关,或者反之亦然,将 Sdc1+/- 和野生型胚胎的胚胎转移到另一种基因型的受体雌性中。在这里,我们表明 Sdc1 的表达减少导致胎儿和母体代谢发生改变,这可能在人类妊娠病理和缺乏 Sdc1 的小鼠中观察到的生长受限中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/5e72b01fa36a/pone.0219604.g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/8a5a7807e626/pone.0219604.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/52eea6c202ba/pone.0219604.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/854b9c668c25/pone.0219604.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/dc6fccb2954e/pone.0219604.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/ff03f3e1aec8/pone.0219604.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/562d7c860d15/pone.0219604.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/026d30e27f02/pone.0219604.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/ea3d7e45bc51/pone.0219604.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/d3eeb048e894/pone.0219604.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/51f665927a28/pone.0219604.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/8c8a8421abce/pone.0219604.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/cf0f9711d0e3/pone.0219604.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/3d3a119a3ed9/pone.0219604.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/0c87de1c6160/pone.0219604.g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/e2c128d61fc0/pone.0219604.g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/5e72b01fa36a/pone.0219604.g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/8a5a7807e626/pone.0219604.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/52eea6c202ba/pone.0219604.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/854b9c668c25/pone.0219604.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/dc6fccb2954e/pone.0219604.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/ff03f3e1aec8/pone.0219604.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/562d7c860d15/pone.0219604.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/026d30e27f02/pone.0219604.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/ea3d7e45bc51/pone.0219604.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/d3eeb048e894/pone.0219604.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/51f665927a28/pone.0219604.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/8c8a8421abce/pone.0219604.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/cf0f9711d0e3/pone.0219604.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/3d3a119a3ed9/pone.0219604.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/0c87de1c6160/pone.0219604.g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/e2c128d61fc0/pone.0219604.g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6e/6625734/5e72b01fa36a/pone.0219604.g016.jpg

相似文献

1
Metabolic and behavioral parameters of mice with reduced expression of Syndecan-1.Syndecan-1 表达降低的小鼠的代谢和行为参数。
PLoS One. 2019 Jul 12;14(7):e0219604. doi: 10.1371/journal.pone.0219604. eCollection 2019.
2
Physiological and anatomical aspects of the reproduction of mice with reduced Syndecan-1 expression.Syndecan-1 表达降低的小鼠生殖的生理和解剖学方面。
Reprod Biol Endocrinol. 2019 Mar 2;17(1):28. doi: 10.1186/s12958-019-0470-2.
3
Lack of Syndecan-1 produces significant alterations in whole-body composition, metabolism and glucose homeostasis in mice.Syndecan-1的缺失会使小鼠的全身组成、新陈代谢和葡萄糖稳态产生显著变化。
World J Diabetes. 2020 Apr 15;11(4):126-136. doi: 10.4239/wjd.v11.i4.126.
4
Induction of syndecan-1 expression in stromal fibroblasts promotes proliferation of human breast cancer cells.基质成纤维细胞中syndecan-1表达的诱导促进人乳腺癌细胞的增殖。
Cancer Res. 2004 Jan 15;64(2):612-21. doi: 10.1158/0008-5472.can-03-2439.
5
Mice lacking the syndecan-3 gene are resistant to diet-induced obesity.缺乏syndecan-3基因的小鼠对饮食诱导的肥胖具有抗性。
J Clin Invest. 2004 Nov;114(9):1354-60. doi: 10.1172/JCI20631.
6
Transgenic expression of syndecan-1 uncovers a physiological control of feeding behavior by syndecan-3.Syndecan-1的转基因表达揭示了syndecan-3对进食行为的生理控制。
Cell. 2001 Jul 13;106(1):105-16. doi: 10.1016/s0092-8674(01)00415-9.
7
Mammary gland development requires syndecan-1 to create a beta-catenin/TCF-responsive mammary epithelial subpopulation.乳腺发育需要syndecan-1来产生一个β-连环蛋白/TCF反应性乳腺上皮亚群。
Oncogene. 2003 Dec 18;22(58):9243-53. doi: 10.1038/sj.onc.1207217.
8
Cell surface-anchored syndecan-1 ameliorates intestinal inflammation and neutrophil transmigration in ulcerative colitis.细胞表面锚定的syndecan-1可改善溃疡性结肠炎中的肠道炎症和中性粒细胞迁移。
J Cell Mol Med. 2017 Jan;21(1):13-25. doi: 10.1111/jcmm.12934. Epub 2016 Aug 25.
9
Syndecan-1 Acts in Synergy with Tight Junction Through Stat3 Signaling to Maintain Intestinal Mucosal Barrier and Prevent Bacterial Translocation.Syndecan-1通过Stat3信号通路与紧密连接协同作用,维持肠道黏膜屏障并防止细菌移位。
Inflamm Bowel Dis. 2015 Aug;21(8):1894-907. doi: 10.1097/MIB.0000000000000421.
10
Syndecan-1 Promotes Streptococcus pneumoniae Corneal Infection by Facilitating the Assembly of Adhesive Fibronectin Fibrils.Syndecan-1 通过促进黏附性纤维连接蛋白纤维的组装促进肺炎链球菌角膜感染。
mBio. 2020 Dec 8;11(6):e01907-20. doi: 10.1128/mBio.01907-20.

引用本文的文献

1
Antidepressive-like Behavior-Related Metabolomic Signatures of Sigma-1 Receptor Knockout Mice.σ-1受体基因敲除小鼠抗抑郁样行为相关的代谢组学特征
Biomedicines. 2022 Jul 1;10(7):1572. doi: 10.3390/biomedicines10071572.
2
Deconstructing cold-induced brown adipocyte neogenesis in mice.解析冷诱导米色脂肪细胞新生在小鼠体内的作用机制。
Elife. 2022 Jul 18;11:e80167. doi: 10.7554/eLife.80167.
3
Genome-Wide Association Analysis to Search for New Loci Associated with Lifelong Premature Ejaculation Risk in Chinese Male Han Population.全基因组关联分析以寻找中国汉族男性人群中与终身早泄风险相关的新基因座。

本文引用的文献

1
Physiological and anatomical aspects of the reproduction of mice with reduced Syndecan-1 expression.Syndecan-1 表达降低的小鼠生殖的生理和解剖学方面。
Reprod Biol Endocrinol. 2019 Mar 2;17(1):28. doi: 10.1186/s12958-019-0470-2.
2
Neuroendocrine integration of nutritional signals on reproduction.营养信号对生殖的神经内分泌整合
J Mol Endocrinol. 2017 Feb;58(2):R107-R128. doi: 10.1530/JME-16-0212. Epub 2017 Jan 5.
3
Syndecan-1 is required to maintain intradermal fat and prevent cold stress.Syndecan-1是维持真皮内脂肪和预防冷应激所必需的。
World J Mens Health. 2022 Apr;40(2):330-339. doi: 10.5534/wjmh.210084. Epub 2022 Jan 1.
PLoS Genet. 2014 Aug 7;10(8):e1004514. doi: 10.1371/journal.pgen.1004514. eCollection 2014 Aug.
4
Placental syndecan-1 and sulphated glycosaminoglycans are decreased in preeclampsia.子痫前期患者胎盘的syndecan-1和硫酸化糖胺聚糖含量降低。
J Perinat Med. 2014 May;42(3):329-38. doi: 10.1515/jpm-2013-0097.
5
Fasting of mice: a review.禁食小鼠:综述。
Lab Anim. 2013 Oct;47(4):225-40. doi: 10.1177/0023677213501659.
6
FELASA guidelines for the refinement of methods for genotyping genetically-modified rodents: a report of the Federation of European Laboratory Animal Science Associations Working Group.FELASA 指导原则:基因修饰啮齿类动物基因分型方法的优化——欧洲实验动物科学协会联合会工作组的报告。
Lab Anim. 2013 Jul;47(3):134-45. doi: 10.1177/0023677212473918.
7
Cold-induced activation of brown adipose tissue and adipose angiogenesis in mice.冷诱导激活棕色脂肪组织和脂肪血管生成在小鼠。
Nat Protoc. 2012 Mar 1;7(3):606-15. doi: 10.1038/nprot.2012.013.
8
Placental syndecan expression is altered in human idiopathic fetal growth restriction.胎盘黏附素的表达在人类特发性胎儿生长受限中发生改变。
Am J Pathol. 2012 Feb;180(2):693-702. doi: 10.1016/j.ajpath.2011.10.023. Epub 2011 Dec 2.
9
Hematoxylin and eosin staining of tissue and cell sections.组织和细胞切片的苏木精和伊红染色。
CSH Protoc. 2008 May 1;2008:pdb.prot4986. doi: 10.1101/pdb.prot4986.
10
A conserved role for syndecan family members in the regulation of whole-body energy metabolism.黏附素家族成员在全身能量代谢调节中的保守作用。
PLoS One. 2010 Jun 23;5(6):e11286. doi: 10.1371/journal.pone.0011286.