• 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

肝细胞移植改善了中间型枫糖尿症小鼠模型的表型并延长了其生存期。

Hepatocyte transplantation improves phenotype and extends survival in a murine model of intermediate maple syrup urine disease.

作者信息

Skvorak Kristen J, Paul Harbhajan S, Dorko Kenneth, Marongiu Fabio, Ellis Ewa, Chace Donald, Ferguson Carolyn, Gibson K Michael, Homanics Gregg E, Strom Stephen C

机构信息

Department of Human Genetics, University of Pittsburgh, Pennsylvania, USA.

出版信息

Mol Ther. 2009 Jul;17(7):1266-73. doi: 10.1038/mt.2009.99. Epub 2009 May 12.

DOI:10.1038/mt.2009.99
PMID:19436271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2835204/
Abstract

Maple syrup urine disease (MSUD; OMIM 248600) is an inborn error of metabolism of the branched chain alpha-ketoacid dehydrogenase (BCKDH) complex that is treated primarily by dietary manipulation of branched-chain amino acids (BCAA). Dietary restriction is lifelong and compliance is difficult. Liver transplantation significantly improves outcomes; however, alternative therapies are needed. To test novel therapies such as hepatocyte transplantation (HTx), we previously created a murine model of intermediate MSUD (iMSUD), which closely mimics human iMSUD. LacZ-positive murine donor hepatocytes were harvested and directly injected (10(5) cells/50 microl) into liver of iMSUD mice (two injections at 1-10 days of age). Donor hepatocytes engrafted into iMSUD recipient liver, increased liver BCKDH activity, improved blood total BCAA/alanine ratio, increased body weight at weaning, and extended the lifespan of HTx-treated iMSUD mice compared to phosphate-buffered saline (PBS)-treated and untreated iMSUD mice. Based on these data demonstrating partial metabolic correction of iMSUD in a murine model, coupled to the fact that multiple transplants are possible to enhance these results, we suggest that HTx represents a promising therapeutic intervention for MSUD that warrants further investigation.

摘要

枫糖尿症(MSUD;OMIM 248600)是一种支链α-酮酸脱氢酶(BCKDH)复合体的先天性代谢缺陷疾病,主要通过对支链氨基酸(BCAA)进行饮食调控来治疗。饮食限制是终身的,且患者很难坚持。肝移植可显著改善治疗效果;然而,仍需要其他替代疗法。为了测试诸如肝细胞移植(HTx)等新疗法,我们之前创建了一种中度MSUD(iMSUD)的小鼠模型,该模型与人类iMSUD极为相似。收集LacZ阳性的小鼠供体肝细胞,并将其直接注射(10⁵个细胞/50微升)到iMSUD小鼠的肝脏中(在1-10日龄时进行两次注射)。供体肝细胞植入到iMSUD受体肝脏中,提高了肝脏BCKDH活性,改善了血液中总BCAA/丙氨酸比值,增加了断奶时的体重,并且与磷酸盐缓冲盐水(PBS)处理和未处理的iMSUD小鼠相比,延长了接受HTx治疗的iMSUD小鼠的寿命。基于这些数据表明在小鼠模型中iMSUD得到了部分代谢纠正,再加上多次移植有可能增强这些结果这一事实,我们认为HTx是一种有前景的MSUD治疗干预手段,值得进一步研究。

相似文献

1
Hepatocyte transplantation improves phenotype and extends survival in a murine model of intermediate maple syrup urine disease.肝细胞移植改善了中间型枫糖尿症小鼠模型的表型并延长了其生存期。
Mol Ther. 2009 Jul;17(7):1266-73. doi: 10.1038/mt.2009.99. Epub 2009 May 12.
2
Placental stem cell correction of murine intermediate maple syrup urine disease.胎盘干细胞纠正鼠类中间型枫糖尿症。
Hepatology. 2013 Mar;57(3):1017-23. doi: 10.1002/hep.26150. Epub 2013 Feb 15.
3
Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD).肝细胞移植(HTx)可纠正小鼠中间型枫糖尿症(iMSUD)中某些神经代谢异常。
Biochim Biophys Acta. 2009 Oct;1792(10):1004-10. doi: 10.1016/j.bbadis.2009.08.006. Epub 2009 Aug 19.
4
Muscle-directed AAV gene therapy rescues the maple syrup urine disease phenotype in a mouse model.肌肉导向的 AAV 基因治疗挽救了小鼠模型中的枫糖尿症表型。
Mol Genet Metab. 2021 Sep-Oct;134(1-2):139-146. doi: 10.1016/j.ymgme.2021.08.003. Epub 2021 Aug 17.
5
Improved amino acid, bioenergetic metabolite and neurotransmitter profiles following human amnion epithelial cell transplant in intermediate maple syrup urine disease mice.人羊膜上皮细胞移植后中间型枫糖尿症小鼠的氨基酸、生物能量代谢物和神经递质谱改善。
Mol Genet Metab. 2013 Jun;109(2):132-8. doi: 10.1016/j.ymgme.2013.02.011. Epub 2013 Feb 26.
6
Production and characterization of murine models of classic and intermediate maple syrup urine disease.经典型和中间型枫糖尿症小鼠模型的构建与特性分析
BMC Med Genet. 2006 Mar 31;7:33. doi: 10.1186/1471-2350-7-33.
7
Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes.支链α-酮酸脱氢酶缺乏症(枫糖尿症):治疗、生物标志物和结局。
Mol Genet Metab. 2020 Mar;129(3):193-206. doi: 10.1016/j.ymgme.2020.01.006. Epub 2020 Jan 16.
8
Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.脂肪移植治疗小鼠支链氨基酸代谢障碍的先天缺陷
Mol Genet Metab. 2013 Aug;109(4):345-53. doi: 10.1016/j.ymgme.2013.05.010. Epub 2013 May 30.
9
Animal models of maple syrup urine disease.枫糖尿症的动物模型。
J Inherit Metab Dis. 2009 Apr;32(2):229-46. doi: 10.1007/s10545-009-1086-z. Epub 2009 Mar 9.
10
Developmental Defects of Caenorhabditis elegans Lacking Branched-chain α-Ketoacid Dehydrogenase Are Mainly Caused by Monomethyl Branched-chain Fatty Acid Deficiency.缺乏支链α-酮酸脱氢酶的秀丽隐杆线虫的发育缺陷主要由单甲基支链脂肪酸缺乏引起。
J Biol Chem. 2016 Feb 5;291(6):2967-73. doi: 10.1074/jbc.M115.676650. Epub 2015 Dec 18.

引用本文的文献

1
Postnatal hyperglycemia alters amino acid profile in retinas (model of Phase I ROP).产后高血糖会改变视网膜中的氨基酸谱(I期视网膜病变模型)。
iScience. 2023 Sep 22;26(10):108021. doi: 10.1016/j.isci.2023.108021. eCollection 2023 Oct 20.
2
Amniotic Membrane and Its Derivatives: Novel Therapeutic Modalities in Liver Disorders.羊膜及其衍生物:肝脏疾病治疗的新方法。
Cells. 2023 Aug 21;12(16):2114. doi: 10.3390/cells12162114.
3
Hyperactivation of mTOR and AKT in a cardiac hypertrophy animal model of Friedreich ataxia.弗里德赖希共济失调心脏肥大动物模型中mTOR和AKT的过度激活。
Heliyon. 2022 Aug 23;8(8):e10371. doi: 10.1016/j.heliyon.2022.e10371. eCollection 2022 Aug.
4
Hepatic Regeneration in Cirrhosis.肝硬化中的肝再生
J Clin Exp Hepatol. 2022 Mar-Apr;12(2):603-616. doi: 10.1016/j.jceh.2021.08.029. Epub 2021 Sep 4.
5
Liver transplantation for pediatric inherited metabolic liver diseases.小儿遗传性代谢性肝病的肝移植
World J Hepatol. 2021 Oct 27;13(10):1351-1366. doi: 10.4254/wjh.v13.i10.1351.
6
Clinical perspective on the use of human amniotic epithelial cells to treat congenital metabolic diseases with a focus on maple syrup urine disease.临床视角下应用人羊膜上皮细胞治疗先天性代谢疾病:以枫糖尿症为例。
Stem Cells Transl Med. 2021 Jun;10(6):829-835. doi: 10.1002/sctm.20-0225. Epub 2021 Feb 6.
7
[Maple syrup urine disease and gene mutations in twin neonates].[枫糖尿症与双胎新生儿的基因突变]
Zhongguo Dang Dai Er Ke Za Zhi. 2016 Dec;18(12):1242-1246. doi: 10.7499/j.issn.1008-8830.2016.12.009.
8
Metformin inhibits Branched Chain Amino Acid (BCAA) derived ketoacidosis and promotes metabolic homeostasis in MSUD.二甲双胍可抑制支链氨基酸(BCAA)衍生的酮酸中毒,并促进 MSUD 中的代谢平衡。
Sci Rep. 2016 Jul 4;6:28775. doi: 10.1038/srep28775.
9
Overexpression of transcription factor Foxa2 and Hnf1α induced rat bone mesenchymal stem cells into hepatocytes.转录因子Foxa2和Hnf1α的过表达将大鼠骨髓间充质干细胞诱导为肝细胞。
Cytotechnology. 2016 Oct;68(5):2037-47. doi: 10.1007/s10616-016-9944-7. Epub 2016 Jan 21.
10
Dynamic Arginine Methylation of Tumor Necrosis Factor (TNF) Receptor-associated Factor 6 Regulates Toll-like Receptor Signaling.肿瘤坏死因子(TNF)受体相关因子6的动态精氨酸甲基化调控Toll样受体信号传导。
J Biol Chem. 2015 Sep 4;290(36):22236-49. doi: 10.1074/jbc.M115.653543. Epub 2015 Jul 28.

本文引用的文献

1
Dual mechanism of brain injury and novel treatment strategy in maple syrup urine disease.枫糖尿症脑损伤的双重机制及新治疗策略
Brain. 2009 Apr;132(Pt 4):903-18. doi: 10.1093/brain/awp024. Epub 2009 Mar 17.
2
Animal models of maple syrup urine disease.枫糖尿症的动物模型。
J Inherit Metab Dis. 2009 Apr;32(2):229-46. doi: 10.1007/s10545-009-1086-z. Epub 2009 Mar 9.
3
Ex vivo gene transfer into hepatocytes.肝细胞的体外基因转移。
Methods Mol Biol. 2009;481:117-40. doi: 10.1007/978-1-59745-201-4_11.
4
Correction of hyperoxaluria by liver repopulation with hepatocytes in a mouse model of primary hyperoxaluria type-1.在1型原发性高草酸尿症小鼠模型中,通过肝细胞重新填充肝脏来纠正高草酸尿症。
Transplantation. 2008 May 15;85(9):1253-60. doi: 10.1097/TP.0b013e31816de49e.
5
Hepatocyte transplantation for glycogen storage disease type Ib.肝细胞移植治疗Ⅰb型糖原贮积病。
Cell Transplant. 2007;16(6):629-37. doi: 10.3727/000000007783465019.
6
Hepatocyte transplantation: clinical experience and potential for future use.肝细胞移植:临床经验及未来应用潜力
Cell Transplant. 2006;15 Suppl 1:S105-10. doi: 10.3727/000000006783982395.
7
Production and characterization of murine models of classic and intermediate maple syrup urine disease.经典型和中间型枫糖尿症小鼠模型的构建与特性分析
BMC Med Genet. 2006 Mar 31;7:33. doi: 10.1186/1471-2350-7-33.
8
Elective liver transplantation for the treatment of classical maple syrup urine disease.择期肝移植治疗经典型枫糖尿症。
Am J Transplant. 2006 Mar;6(3):557-64. doi: 10.1111/j.1600-6143.2005.01209.x.
9
Administration-route and gender-independent long-term therapeutic correction of phenylketonuria (PKU) in a mouse model by recombinant adeno-associated virus 8 pseudotyped vector-mediated gene transfer.通过重组腺相关病毒8假型载体介导的基因转移,在小鼠模型中对苯丙酮尿症(PKU)进行与给药途径和性别无关的长期治疗性矫正
Gene Ther. 2006 Apr;13(7):587-93. doi: 10.1038/sj.gt.3302684.
10
Hepatocyte transplantation for inherited factor VII deficiency.肝细胞移植治疗遗传性因子VII缺乏症。
Transplantation. 2004 Dec 27;78(12):1812-4. doi: 10.1097/01.tp.0000146386.77076.47.