• 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

Bone marrow transplant in a case of mucopolysaccharidosis I Scheie phenotype: skin ultrastructure before and after transplantation.

作者信息

Navarro C, Dominguez C, Costa M, Ortega J J

机构信息

Division of Neuropathology, Hospital Infantil, Ciudad Sanitaria Valle de Hebrón, Universidad Autónoma, Barcelona, Spain.

出版信息

Acta Neuropathol. 1991;82(1):33-8. doi: 10.1007/BF00310920.

DOI:10.1007/BF00310920
PMID:1950476
Abstract

An 11-year-old girl with mucopolysaccharidosis I Scheie phenotype (MPS I-S) received a bone marrow transplant (BMT) from her heterozygous HLA-identical LMC-non-reactive mother. Multidisciplinary studies were carried out and results evaluated 21 months after transplantation. Herein we report the ultrastructural findings pre- and post-BMT in skin. Multidisciplinary studies are commonly used to evaluate the benefits of metabolic correction following BMT in some MPS and other inherited metabolic disorders, and changes in morphology have been described in liver and few other tissues. In this case, we elected skin, since connective tissue is universally involved in MPS and is safely and easily obtainable. Comparison of skin biopsy specimens taken before and after BMT showed a considerable change in dermal fibroblast morphology, with marked reduction in cell size and the number and size of abnormal lysosomes, thus indicating the clearance of storage. Our results demonstrate that dermal cells respond to enzyme replacement therapy in MPS I-S, with the clearance of glycosaminoglycan lysosomal accumulation in connective tissue fibroblasts, which had near-normal morphology 21 months after BMT. Therefore, the practice of skin biopsy after BMT in MPS and other metabolic disorders in which dermal cells are involved should be encouraged.

摘要

相似文献

1
Bone marrow transplant in a case of mucopolysaccharidosis I Scheie phenotype: skin ultrastructure before and after transplantation.
Acta Neuropathol. 1991;82(1):33-8. doi: 10.1007/BF00310920.
2
Stereological and morphometric analysis of dermal fibroblasts before and after bone marrow transplantation in a case of mucopolysaccharidosis I Scheie phenotype.黏多糖贮积症I型Scheie表型病例中骨髓移植前后真皮成纤维细胞的体视学和形态计量学分析
Acta Neuropathol. 1993;86(1):21-8. doi: 10.1007/BF00454894.
3
[Bone marrow transplantation in mucopolysaccharidosis type I, Hurler-Scheie variety. Metabolic correction and clinical results].
An Esp Pediatr. 1990 Oct;33(4):369-75.
4
Bone marrow transplantation for feline mucopolysaccharidosis I.猫黏多糖贮积症I型的骨髓移植
Mol Genet Metab. 2007 Jul;91(3):239-50. doi: 10.1016/j.ymgme.2007.03.001. Epub 2007 May 7.
5
Long-term effects of bone marrow transplantation in dogs with mucopolysaccharidosis I.骨髓移植对黏多糖贮积症I型犬的长期影响。
Am J Pathol. 1989 Mar;134(3):677-92.
6
Pathology of the liver in mucopolysaccharidosis: light and electron microscopic assessment before and after bone marrow transplantation.黏多糖贮积症的肝脏病理学:骨髓移植前后的光镜和电镜评估
Bone Marrow Transplant. 1992 Sep;10(3):273-80.
7
Impaired bone remodeling and its correction by combination therapy in a mouse model of mucopolysaccharidosis-I.黏多糖贮积症 I 型小鼠模型中骨重塑受损及其联合治疗矫正
Hum Mol Genet. 2015 Dec 15;24(24):7075-86. doi: 10.1093/hmg/ddv407. Epub 2015 Oct 1.
8
Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotype.具有明确基因型的骨髓移植I型黏多糖贮积症患者的长期临床进展
J Inherit Metab Dis. 1993;16(6):1024-33. doi: 10.1007/BF00711520.
9
Bone marrow transplantation in newborn rats with mucopolysaccharidosis type VI: biochemical, pathological, and clinical findings.新生黏多糖贮积症VI型大鼠的骨髓移植:生化、病理及临床发现
Transplantation. 1997 May 27;63(10):1386-93. doi: 10.1097/00007890-199705270-00003.
10
Residual α-L-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients.黏多糖贮积症 I 型患者的成纤维细胞中残留的α-L-艾杜糖苷酸酶活性。
Mol Genet Metab. 2013 Aug;109(4):377-81. doi: 10.1016/j.ymgme.2013.05.016. Epub 2013 Jun 4.

引用本文的文献

1
Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome.马罗-拉米综合征猫模型中的酶替代疗法。
J Clin Invest. 1996 Apr 15;97(8):1864-73. doi: 10.1172/JCI118617.
2
Stereological and morphometric analysis of dermal fibroblasts before and after bone marrow transplantation in a case of mucopolysaccharidosis I Scheie phenotype.黏多糖贮积症I型Scheie表型病例中骨髓移植前后真皮成纤维细胞的体视学和形态计量学分析
Acta Neuropathol. 1993;86(1):21-8. doi: 10.1007/BF00454894.
3
Nerve biopsy findings in Niemann-Pick type II (NPC).尼曼-匹克病II型(NPC)的神经活检结果。

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
The uptake of enzymes into lysosomes: an overview.酶进入溶酶体的过程:概述
Birth Defects Orig Artic Ser. 1980;16(1):77-84.
3
Correction of feline arylsulphatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation.通过骨髓移植纠正猫的芳基硫酸酯酶B缺乏症(粘多糖贮积症VI型)
Acta Neuropathol. 1994;88(6):602-3. doi: 10.1007/BF00296502.
Nature. 1984;312(5993):467-9. doi: 10.1038/312467a0.
4
Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases.黏多糖贮积症的产前病理学:与产后病例的比较
Clin Neuropathol. 1983;2(3):122-7.
5
Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Biochemical and clinical status 24 months after transplantation.马洛托-拉米综合征(黏多糖贮积症 VI 型)的骨髓移植。移植后 24 个月的生化和临床状况。
N Engl J Med. 1984 Dec 20;311(25):1606-11. doi: 10.1056/NEJM198412203112504.
6
Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation.骨髓移植治疗后,黏多糖贮积症I型临床特征的逆转及生化指标的改善。
Lancet. 1981 Oct 3;2(8249):709-12. doi: 10.1016/s0140-6736(81)91046-1.
7
Ultrastructure of the skin in the genetic mucopolysaccharidoses.遗传性黏多糖贮积症患者皮肤的超微结构
Arch Pathol. 1972 Dec;94(6):511-8.
8
The clinical spectrum of alpha-L-iduronidase deficiency.α-L-艾杜糖醛酸酶缺乏症的临床谱
Am J Med Genet. 1985 Mar;20(3):471-81. doi: 10.1002/ajmg.1320200308.
9
Bone marrow transplantation for Hurler syndrome: assessment of metabolic correction.黏多糖贮积症Ⅰ型的骨髓移植:代谢纠正评估
Birth Defects Orig Artic Ser. 1986;22(1):7-24.
10
Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT.马罗-拉米综合征(黏多糖贮积症6型)的骨髓移植:骨髓移植40个月后的状况
Birth Defects Orig Artic Ser. 1986;22(1):41-53.