• 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

母体低蛋白饮食致成年程序化大鼠肾小体微小 RNA 表达改变与上皮间质转化的关系。

Involvement of renal corpuscle microRNA expression on epithelial-to-mesenchymal transition in maternal low protein diet in adult programmed rats.

机构信息

Fetal Programming Laboratory, Morphology Department, São Paulo State University, Botucatu, São Paulo, Brazil.

出版信息

PLoS One. 2013 Aug 19;8(8):e71310. doi: 10.1371/journal.pone.0071310. eCollection 2013.

DOI:10.1371/journal.pone.0071310
PMID:23977013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3747155/
Abstract

Prior study shows that maternal protein-restricted (LP) 16-wk-old offspring have pronounced reduction of nephron number and arterial hypertension associated with unchanged glomerular filtration rate, besides enhanced glomerular area, which may be related to glomerular hyperfiltration/overflow and which accounts for the glomerular filtration barrier breakdown and early glomerulosclerosis. In the current study, LP rats showed heavy proteinuria associated with podocyte simplification and foot process effacement. TGF-β1 glomerular expression was significantly enhanced in LP. Isolated LP glomeruli show a reduced level of miR-200a, miR-141, miR-429 and ZEB2 mRNA and upregulated collagen 1α1/2 mRNA expression. By western blot analyzes of whole kidney tissue, we found significant reduction of both podocin and nephrin and enhanced expression of mesenchymal protein markers such as desmin, collagen type I and fibronectin. From our present knowledge, these are the first data showing renal miRNA modulation in the protein restriction model of fetal programming. The fetal-programmed adult offspring showed pronounced structural glomerular disorders with an accentuated and advanced stage of fibrosis, which led us to state that the glomerular miR-200 family would be downregulated by TGF-β1 action inducing ZEB 2 expression that may subsequently cause glomeruli epithelial-to-mesenchymal transition.

摘要

先前的研究表明,母源性蛋白质限制(LP)16 周龄的后代的肾单位数量明显减少,同时伴有动脉高血压,但肾小球滤过率不变,此外肾小球面积增加,这可能与肾小球高滤过/超负荷有关,是肾小球滤过屏障破坏和早期肾小球硬化的原因。在本研究中,LP 大鼠表现出大量蛋白尿,伴有足细胞简化和足突消失。LP 肾小球中 TGF-β1 的表达显著增强。分离的 LP 肾小球显示 miR-200a、miR-141、miR-429 和 ZEB2mRNA 水平降低,胶原 1α1/2mRNA 表达上调。通过对全肾组织的 Western blot 分析,我们发现 podocin 和 nephrin 的表达明显减少,间充质蛋白标志物如结蛋白、I 型胶原和纤维连接蛋白的表达增强。就我们目前的知识而言,这些是首次在胎儿编程的蛋白质限制模型中显示肾脏 miRNA 调节的研究数据。胎儿编程的成年后代表现出明显的结构性肾小球病变,纤维化程度加重且处于更高级阶段,这使我们认为肾小球 miR-200 家族可能会被 TGF-β1 诱导的 ZEB2 表达下调,从而导致肾小球上皮细胞向间充质转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/21a645df920b/pone.0071310.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/e4916ba8f1b4/pone.0071310.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/8e724426951a/pone.0071310.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/49fe185d2ad6/pone.0071310.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/c6274903f62f/pone.0071310.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/f8b95c20ee0d/pone.0071310.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/d36024418ae3/pone.0071310.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/44ab3a626728/pone.0071310.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/6b0451d0e1e6/pone.0071310.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/21a645df920b/pone.0071310.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/e4916ba8f1b4/pone.0071310.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/8e724426951a/pone.0071310.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/49fe185d2ad6/pone.0071310.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/c6274903f62f/pone.0071310.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/f8b95c20ee0d/pone.0071310.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/d36024418ae3/pone.0071310.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/44ab3a626728/pone.0071310.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/6b0451d0e1e6/pone.0071310.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637b/3747155/21a645df920b/pone.0071310.g011.jpg

相似文献

1
Involvement of renal corpuscle microRNA expression on epithelial-to-mesenchymal transition in maternal low protein diet in adult programmed rats.母体低蛋白饮食致成年程序化大鼠肾小体微小 RNA 表达改变与上皮间质转化的关系。
PLoS One. 2013 Aug 19;8(8):e71310. doi: 10.1371/journal.pone.0071310. eCollection 2013.
2
Gestational low-protein intake enhances whole-kidney miR-192 and miR-200 family expression and epithelial-to-mesenchymal transition in rat adult male offspring.低蛋白饮食可增强大鼠成年雄性子代肾脏全组织 miR-192 和 miR-200 家族表达并促进上皮-间充质转化。
J Exp Biol. 2018 May 22;221(Pt 10):jeb171694. doi: 10.1242/jeb.171694.
3
Gestational and Breastfeeding Low-Protein Intake on Blood Pressure, Kidney Structure, and Renal Function in Male Rat Offspring in Adulthood.孕期及哺乳期低蛋白摄入对雄性大鼠成年后代血压、肾脏结构和肾功能的影响
Front Physiol. 2021 Apr 22;12:658431. doi: 10.3389/fphys.2021.658431. eCollection 2021.
4
Role of MiR-155 Signal Pathway in Regulating Podocyte Injury Induced by TGF-β1.微小RNA-155信号通路在调节转化生长因子-β1诱导的足细胞损伤中的作用
Cell Physiol Biochem. 2017;42(4):1469-1480. doi: 10.1159/000479211. Epub 2017 Jul 18.
5
Adenovirus-mediated gene transfer of TGF-β1 to the renal glomeruli leads to proteinuria.腺病毒介导的 TGF-β1 基因转移到肾小球导致蛋白尿。
Am J Pathol. 2012 Mar;180(3):940-951. doi: 10.1016/j.ajpath.2011.11.023. Epub 2011 Dec 25.
6
Temporal and spatial expression of podocyte-associated molecules are accompanied by proteinuria in IgA nephropathy rat model.在 IgA 肾病大鼠模型中,足细胞相关分子的时空表达伴随着蛋白尿。
Physiol Res. 2013;62(1):35-45. doi: 10.33549/physiolres.932380. Epub 2012 Nov 22.
7
Selective phosphodiesterase-5 (PDE-5) inhibitor vardenafil ameliorates renal damage in type 1 diabetic rats by restoring cyclic 3',5' guanosine monophosphate (cGMP) level in podocytes.选择性磷酸二酯酶-5(PDE-5)抑制剂伐地那非通过恢复足细胞中环鸟苷酸(cGMP)水平改善 1 型糖尿病大鼠的肾损伤。
Nephrol Dial Transplant. 2013 Jul;28(7):1751-61. doi: 10.1093/ndt/gfs391. Epub 2012 Nov 29.
8
Implication of CD38 gene in podocyte epithelial-to-mesenchymal transition and glomerular sclerosis.CD38 基因在足细胞上皮-间充质转化及肾小球硬化中的作用
J Cell Mol Med. 2012 Aug;16(8):1674-85. doi: 10.1111/j.1582-4934.2011.01462.x.
9
Mesenchymal stem cells ameliorate podocyte injury and proteinuria in a type 1 diabetic nephropathy rat model.间充质干细胞改善 1 型糖尿病肾病大鼠模型的足细胞损伤和蛋白尿。
Biol Blood Marrow Transplant. 2013 Apr;19(4):538-46. doi: 10.1016/j.bbmt.2013.01.001. Epub 2013 Jan 4.
10
Epithelial-to-mesenchymal transition is a potential pathway leading to podocyte dysfunction and proteinuria.上皮-间充质转化是导致足细胞功能障碍和蛋白尿的潜在途径。
Am J Pathol. 2008 Feb;172(2):299-308. doi: 10.2353/ajpath.2008.070057. Epub 2008 Jan 17.

引用本文的文献

1
Early and long-term effects of maternal protein restriction on offspring organs and systems: insights from the developmental origins of health and disease (DOHaD).母体蛋白质限制对后代器官和系统的早期及长期影响:来自健康与疾病的发育起源(DOHaD)的见解
Biogerontology. 2025 Aug 28;26(5):175. doi: 10.1007/s10522-025-10316-w.
2
Nutrition and Developmental Origins of Kidney Disease.营养与肾脏疾病的发育起源
Nutrients. 2023 Sep 29;15(19):4207. doi: 10.3390/nu15194207.
3
The function of miRNAs in the process of kidney development.微小RNA在肾脏发育过程中的作用。

本文引用的文献

1
De novo expression of podocyte proteins in parietal epithelial cells in experimental aging nephropathy.实验性衰老肾病中壁层上皮细胞中足细胞蛋白的从头表达。
Am J Physiol Renal Physiol. 2012 Mar 1;302(5):F571-80. doi: 10.1152/ajprenal.00516.2011. Epub 2011 Nov 30.
2
The miR-200 family regulates TGF-β1-induced renal tubular epithelial to mesenchymal transition through Smad pathway by targeting ZEB1 and ZEB2 expression.miR-200 家族通过靶向 ZEB1 和 ZEB2 的表达来调控 TGF-β1 诱导的肾小管所上皮到间质的转化,这一过程是通过 Smad 通路实现的。
Am J Physiol Renal Physiol. 2012 Feb 1;302(3):F369-79. doi: 10.1152/ajprenal.00268.2011. Epub 2011 Oct 19.
3
Noncoding RNA Res. 2023 Aug 23;8(4):593-601. doi: 10.1016/j.ncrna.2023.08.009. eCollection 2023 Dec.
4
Vitamin D deficiency contributes to the diabetic kidney disease progression via increase ZEB1/ZEB2 expressions.维生素 D 缺乏通过增加 ZEB1/ZEB2 的表达促进糖尿病肾病的进展。
Nutr Diabetes. 2023 Jul 1;13(1):9. doi: 10.1038/s41387-023-00238-2.
5
Impact of maternal protein restriction on Hypoxia-Inducible Factor (HIF) expression in male fetal kidney development.母体蛋白质限制对雄性胎儿肾脏发育中缺氧诱导因子 (HIF) 表达的影响。
PLoS One. 2023 May 4;18(5):e0266293. doi: 10.1371/journal.pone.0266293. eCollection 2023.
6
Transcriptome and morphological analysis on the heart in gestational protein-restricted aging male rat offspring.孕期蛋白质限制的老龄雄性大鼠后代心脏的转录组和形态学分析
Front Cell Dev Biol. 2022 Oct 24;10:892322. doi: 10.3389/fcell.2022.892322. eCollection 2022.
7
Fetal Undernutrition Programming, Sympathetic Nerve Activity, and Arterial Hypertension Development.胎儿营养不足编程、交感神经活动与动脉高血压的发生
Front Physiol. 2021 Nov 17;12:704819. doi: 10.3389/fphys.2021.704819. eCollection 2021.
8
Gestational Low Protein Diet Modulation on miRNA Transcriptome and Its Target During Fetal and Breastfeeding Nephrogenesis.孕期低蛋白饮食对胎儿及哺乳期肾脏发育过程中miRNA转录组及其靶标的调控作用
Front Physiol. 2021 Jun 22;12:648056. doi: 10.3389/fphys.2021.648056. eCollection 2021.
9
Gestational and Breastfeeding Low-Protein Intake on Blood Pressure, Kidney Structure, and Renal Function in Male Rat Offspring in Adulthood.孕期及哺乳期低蛋白摄入对雄性大鼠成年后代血压、肾脏结构和肾功能的影响
Front Physiol. 2021 Apr 22;12:658431. doi: 10.3389/fphys.2021.658431. eCollection 2021.
10
Targeting the Renin-Angiotensin-Aldosterone System to Prevent Hypertension and Kidney Disease of Developmental Origins.针对肾素-血管紧张素-醛固酮系统预防发育起源性高血压和肾脏疾病。
Int J Mol Sci. 2021 Feb 25;22(5):2298. doi: 10.3390/ijms22052298.
The role of EMT in renal fibrosis.
EMT 在肾纤维化中的作用。
Cell Tissue Res. 2012 Jan;347(1):103-16. doi: 10.1007/s00441-011-1227-1. Epub 2011 Aug 16.
4
Mechanisms and consequences of TGF-ß overexpression by podocytes in progressive podocyte disease.足细胞 TGF-β过表达在进行性足细胞病中的机制和后果。
Cell Tissue Res. 2012 Jan;347(1):129-40. doi: 10.1007/s00441-011-1169-7. Epub 2011 May 4.
5
Maternal undernutrition and the offspring kidney: from fetal to adult life.母体营养不足与后代肾脏:从胎儿到成年期。
Braz J Med Biol Res. 2010 Nov;43(11):1010-8. doi: 10.1590/s0100-879x2010007500113. Epub 2010 Oct 29.
6
miR-200a Prevents renal fibrogenesis through repression of TGF-β2 expression.miR-200a 通过抑制 TGF-β2 的表达来防止肾纤维化。
Diabetes. 2011 Jan;60(1):280-7. doi: 10.2337/db10-0892. Epub 2010 Oct 15.
7
Mechanisms of tubulointerstitial fibrosis.肾小管间质纤维化的机制。
J Am Soc Nephrol. 2010 Nov;21(11):1819-34. doi: 10.1681/ASN.2010080793. Epub 2010 Sep 23.
8
miR-192 mediates TGF-beta/Smad3-driven renal fibrosis.miR-192 介导 TGF-β/Smad3 驱动的肾脏纤维化。
J Am Soc Nephrol. 2010 Aug;21(8):1317-25. doi: 10.1681/ASN.2010020134. Epub 2010 May 20.
9
E-cadherin expression is regulated by miR-192/215 by a mechanism that is independent of the profibrotic effects of transforming growth factor-beta.E-钙黏蛋白的表达受 miR-192/215 调控,其机制与转化生长因子-β的促纤维化作用无关。
Diabetes. 2010 Jul;59(7):1794-802. doi: 10.2337/db09-1736. Epub 2010 Apr 14.
10
New insights into epithelial-mesenchymal transition in kidney fibrosis.上皮-间质转化在肾纤维化中的新认识。
J Am Soc Nephrol. 2010 Feb;21(2):212-22. doi: 10.1681/ASN.2008121226. Epub 2009 Dec 17.