• 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

黏多糖贮积症 I 型(MPS I)小鼠模型中雄性附属性腺的形态学描述。

Morphologic description of male reproductive accessory glands in a mouse model of mucopolysaccharidosis type I (MPS I).

机构信息

Department of Psychobiology, Universidade Federal de São Paulo, 925, Napoleão de Barros St, 3rd Floor, São Paulo, SP, 04024-002, Brazil.

Department of Biosciences, Universidade Federal de São Paulo, Santos, SP, Brazil.

出版信息

J Mol Histol. 2020 Apr;51(2):137-145. doi: 10.1007/s10735-020-09864-x. Epub 2020 Mar 11.

DOI:10.1007/s10735-020-09864-x
PMID:32162173
Abstract

Mucopolysaccharidosis type I (MPS I) is a genetic disease caused by a deficiency of the lysosomal hydrolase α-L-iduronidase (IDUA). IDUA degrades two types of glycosaminoglycans (GAGs): heparan and dermatan sulfates, important components of extracellular matrix, with signaling and structural functions. The accumulation of GAGs results in progressive physiological impairments in a variety of tissues, making MPS I a complex and multisystemic disease. Due the advent of therapeutic strategies which have increased patients' life expectancy, our group have been investigating the effect of IDUA deficiency on the reproductive system. In the present study, we aimed to characterize some of the accessory glands of the male reproductive tract in an MPS I mouse model. We used 6-month-old Idua+/+ and Idua-/- male mice to evaluate the histology of the seminal vesicles and prostate. Interstitial deposits of GAGs and collagen fibers were also observed. Seminal vesicles were smaller in the Idua-/- group, regardless of the normal staining pattern of the epithelial cells, marked with antiandrogen receptor. The prostate of Idua-/- mice presented necrotic acini and increased deposition of collagen fibers in the interstitium. All glands presented evident deposits of GAGs in the extracellular matrix, especially inside vacuolated interstitial cells. We concluded that, at this stage of the disease, the prostate is the most damaged accessory gland and may therefore, be the first to manifest functional impairments during disease progression.

摘要

黏多糖贮积症 I 型(MPS I)是一种由溶酶体水解酶α-L-艾杜糖苷酸酶(IDUA)缺乏引起的遗传性疾病。IDUA 降解两种类型的糖胺聚糖(GAG):肝素和硫酸皮肤素,它们是细胞外基质的重要成分,具有信号和结构功能。GAG 的积累导致各种组织中进行性生理损伤,使 MPS I 成为一种复杂的多系统疾病。由于治疗策略的出现提高了患者的预期寿命,我们的研究小组一直在研究 IDUA 缺乏对生殖系统的影响。在本研究中,我们旨在描述 MPS I 小鼠模型中男性生殖系统的一些附属腺体。我们使用 6 个月大的 Idua+/+和 Idua-/-雄性小鼠来评估精囊和前列腺的组织学。还观察到 GAG 和胶原纤维的间质沉积物。无论上皮细胞的正常染色模式如何,IDua-/- 组的精囊都较小,用抗雄激素受体标记。IDua-/- 小鼠的前列腺呈现出坏死的腺泡和间质中胶原纤维的增加沉积。所有腺体在细胞外基质中都有明显的 GAG 沉积,尤其是在空泡化的间质细胞内。我们得出结论,在疾病的这个阶段,前列腺是最受损的附属腺体,因此可能是在疾病进展过程中最早表现出功能障碍的腺体。

相似文献

1
Morphologic description of male reproductive accessory glands in a mouse model of mucopolysaccharidosis type I (MPS I).黏多糖贮积症 I 型(MPS I)小鼠模型中雄性附属性腺的形态学描述。
J Mol Histol. 2020 Apr;51(2):137-145. doi: 10.1007/s10735-020-09864-x. Epub 2020 Mar 11.
2
Evidence that glycosaminoglycan storage and collagen deposition in the cauda epididymidis does not impair sperm viability in the Mucopolysaccharidosis type I mouse model.证据表明,黏多糖贮积症 I 型小鼠模型的尾部附睾中糖胺聚糖的储存和胶原沉积并不损害精子活力。
Reprod Fertil Dev. 2020 Feb;32(3):304-312. doi: 10.1071/RD19144.
3
Morphological damage in Sertoli, myoid and interstitial cells in a mouse model of mucopolysaccharidosis type I (MPS I).黏多糖贮积症 I 型(MPS I)小鼠模型中 Sertoli 细胞、肌样细胞和间质细胞的形态损伤。
Mol Biol Rep. 2021 Jan;48(1):363-370. doi: 10.1007/s11033-020-06055-5. Epub 2020 Dec 15.
4
Analysis of male reproductive parameters in a murine model of mucopolysaccharidosis type I (MPS I).I型黏多糖贮积症(MPS I)小鼠模型中雄性生殖参数的分析。
Int J Clin Exp Pathol. 2014 May 15;7(6):3488-97. eCollection 2014.
5
Sexual behaviour in a murine model of mucopolysaccharidosis type I (MPS I).黏多糖贮积症Ⅰ型(MPS I)小鼠模型中的性行为。
PLoS One. 2019 Dec 13;14(12):e0220429. doi: 10.1371/journal.pone.0220429. eCollection 2019.
6
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation.一种 MPS I-H 基因敲入小鼠的特征,该小鼠携带一种类似于人类 IDUA-W402X 突变的无义突变。
Mol Genet Metab. 2010 Jan;99(1):62-71. doi: 10.1016/j.ymgme.2009.08.002.
7
Biomechanical and histological characterization of MPS I mice femurs.MPS I 型小鼠股骨的生物力学和组织学特性研究。
Acta Histochem. 2021 Feb;123(2):151678. doi: 10.1016/j.acthis.2020.151678. Epub 2021 Jan 9.
8
Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome.艾杜糖醛酸酶基因敲除小鼠功能减退模拟了黏多糖贮积症I型患者关节功能和运动能力的受限情况。
Orphanet J Rare Dis. 2015 Sep 25;10:121. doi: 10.1186/s13023-015-0337-3.
9
Characterization of joint disease in mucopolysaccharidosis type I mice.黏多糖贮积症 I 型小鼠关节疾病的特征。
Int J Exp Pathol. 2013 Oct;94(5):305-11. doi: 10.1111/iep.12033. Epub 2013 Jun 21.
10
Alterations of membrane lipids and in gene expression of ganglioside metabolism in different brain structures in a mouse model of mucopolysaccharidosis type I (MPS I).黏多糖贮积症Ⅰ型(MPS I)小鼠模型不同脑区神经节苷脂代谢相关基因表达及膜脂改变。
Gene. 2013 Sep 15;527(1):109-14. doi: 10.1016/j.gene.2013.06.002. Epub 2013 Jun 15.

引用本文的文献

1
Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review.溶酶体贮积病动物模型中的繁殖:一项范围综述。
Front Mol Biosci. 2021 Nov 12;8:773384. doi: 10.3389/fmolb.2021.773384. eCollection 2021.

本文引用的文献

1
Sexual behaviour in a murine model of mucopolysaccharidosis type I (MPS I).黏多糖贮积症Ⅰ型(MPS I)小鼠模型中的性行为。
PLoS One. 2019 Dec 13;14(12):e0220429. doi: 10.1371/journal.pone.0220429. eCollection 2019.
2
Evidence that glycosaminoglycan storage and collagen deposition in the cauda epididymidis does not impair sperm viability in the Mucopolysaccharidosis type I mouse model.证据表明,黏多糖贮积症 I 型小鼠模型的尾部附睾中糖胺聚糖的储存和胶原沉积并不损害精子活力。
Reprod Fertil Dev. 2020 Feb;32(3):304-312. doi: 10.1071/RD19144.
3
Pregnancy in patients with mucopolysaccharidosis: a case series.
黏多糖贮积症患者的妊娠:病例系列
Mol Genet Metab Rep. 2016 Aug 29;8:111-5. doi: 10.1016/j.ymgmr.2016.08.002. eCollection 2016 Sep.
4
The mouse prostate: a basic anatomical and histological guideline.小鼠前列腺:基础解剖学与组织学指南。
Bosn J Basic Med Sci. 2016 Feb 10;16(1):8-13. doi: 10.17305/bjbms.2016.917.
5
Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome.艾杜糖醛酸酶基因敲除小鼠功能减退模拟了黏多糖贮积症I型患者关节功能和运动能力的受限情况。
Orphanet J Rare Dis. 2015 Sep 25;10:121. doi: 10.1186/s13023-015-0337-3.
6
Successful pregnancy and breastfeeding in a woman with mucopolysaccharidosis type I while receiving laronidase enzyme replacement. therapy.
Clin Exp Obstet Gynecol. 2015;42(1):108-13.
7
Analysis of male reproductive parameters in a murine model of mucopolysaccharidosis type I (MPS I).I型黏多糖贮积症(MPS I)小鼠模型中雄性生殖参数的分析。
Int J Clin Exp Pathol. 2014 May 15;7(6):3488-97. eCollection 2014.
8
Evidence of a progressive motor dysfunction in Mucopolysaccharidosis type I mice.黏多糖贮积症Ⅰ型小鼠进行性运动功能障碍的证据。
Behav Brain Res. 2012 Jul 15;233(1):169-75. doi: 10.1016/j.bbr.2012.04.051. Epub 2012 May 9.
9
Androgen action in the epididymis.雄激素在附睾中的作用。
J Androl. 2011 Nov-Dec;32(6):592-9. doi: 10.2164/jandrol.111.014266. Epub 2011 Jul 15.
10
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation.一种 MPS I-H 基因敲入小鼠的特征,该小鼠携带一种类似于人类 IDUA-W402X 突变的无义突变。
Mol Genet Metab. 2010 Jan;99(1):62-71. doi: 10.1016/j.ymgme.2009.08.002.