• 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

在一个表皮松解性角化过度小鼠模型中,超微结构正常,但角质层脂质和蛋白质组成发生改变。

Normal ultrastructure, but altered stratum corneum lipid and protein composition in a mouse model for epidermolytic hyperkeratosis.

作者信息

Reichelt J, Doering T, Schnetz E, Fartasch M, Sandhoff K, Magin A M

机构信息

Institut für Genetik and Bonner Forum Biomedizin, Friedrich-Wilhelms-Universität, Bonn, Germany.

出版信息

J Invest Dermatol. 1999 Sep;113(3):329-34. doi: 10.1046/j.1523-1747.1999.00702.x.

DOI:10.1046/j.1523-1747.1999.00702.x
PMID:10469329
Abstract

Recently, we established keratin 10-deficient mice, serving as a model for the hyperkeratotic skin disorder epidermolytic hyperkeratosis. The considerable ichthyosis in these mice suggested alterations in terminal differentiation and in the formation of a functional epidermal barrier. Here, we report on the ultrastructural organization and composition of the stratum corneum lipids and on the expression of two major cornified envelope proteins. Electron microscopy of ruthenium tetroxide postfixed skin samples demonstrated a normal extrusion and morphology of lamellar bodies as well as the formation of bona fide lamellar layers in neonatal keratin 10-deficient mice. When we studied the composition of the major stratum corneum lipids, however, we found significant changes. Most importantly, the analysis of ceramide subpopulations revealed that the total amount of ceramide 2 was elevated in keratin 10-deficient mice, whereas ceramides 1, 3, 4, and 5 were decreased among total stratum corneum lipids. The amount of the ceramide precursors sphingomyelin and glucosylceramide was reduced in the stratum corneum without accompanying changes in the mRNA coding for acid sphingomyelinase. Notably, we found an increased mRNA and protein content for involucrin in neonatal keratin 10-deficient mice, whereas the expression of loricrin was not changed. Our data demonstrate that, although the formation of lipid layers in the stratum corneum appeared to be normal, its lipid composition is significantly altered in keratin 10-deficient mice.

摘要

最近,我们培育出了角蛋白10缺陷型小鼠,作为角化过度性皮肤病——表皮松解性角化过度症的模型。这些小鼠出现的严重鱼鳞病表明其终末分化及功能性表皮屏障的形成发生了改变。在此,我们报告角质层脂质的超微结构组织和组成以及两种主要的角质包膜蛋白的表达情况。对经四氧化锇后固定的皮肤样本进行电子显微镜观察发现,新生角蛋白10缺陷型小鼠的板层小体挤出和形态正常,且形成了真正的板层结构。然而,当我们研究主要角质层脂质的组成时,发现了显著变化。最重要的是,对角质层神经酰胺亚群的分析显示,角蛋白10缺陷型小鼠中神经酰胺2的总量升高,而在总角质层脂质中,神经酰胺1、3、4和5的含量降低。角质层中神经酰胺前体鞘磷脂和葡萄糖神经酰胺的含量减少,而酸性鞘磷脂酶的mRNA编码没有相应变化。值得注意的是,我们发现新生角蛋白10缺陷型小鼠中兜甲蛋白的mRNA和蛋白质含量增加,而loricrin的表达没有变化。我们的数据表明,尽管角质层脂质层的形成似乎正常,但在角蛋白10缺陷型小鼠中其脂质组成发生了显著改变。

相似文献

1
Normal ultrastructure, but altered stratum corneum lipid and protein composition in a mouse model for epidermolytic hyperkeratosis.在一个表皮松解性角化过度小鼠模型中,超微结构正常,但角质层脂质和蛋白质组成发生改变。
J Invest Dermatol. 1999 Sep;113(3):329-34. doi: 10.1046/j.1523-1747.1999.00702.x.
2
Impaired cutaneous permeability barrier function, skin hydration, and sphingomyelinase activity in keratin 10 deficient mice.角蛋白10缺陷小鼠的皮肤渗透屏障功能受损、皮肤水合作用及鞘磷脂酶活性降低。
J Invest Dermatol. 2000 Oct;115(4):708-13. doi: 10.1046/j.1523-1747.2000.00103.x.
3
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosis.表皮松解性角化过度症中通透性屏障异常的发病机制。
J Invest Dermatol. 2001 Oct;117(4):837-47. doi: 10.1046/j.0022-202x.2001.01471.x.
4
Aberrant lipid organization in stratum corneum of patients with atopic dermatitis and lamellar ichthyosis.特应性皮炎和板层状鱼鳞病患者角质层中异常的脂质组织。
J Invest Dermatol. 2001 Sep;117(3):710-7. doi: 10.1046/j.0022-202x.2001.01455.x.
5
Altered distribution of keratinization markers in epidermolytic hyperkeratosis.表皮松解性角化过度中角化标记物分布的改变。
Arch Dermatol Res. 1995;287(8):705-11. doi: 10.1007/BF01105793.
6
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis).丝聚合蛋白在表皮松解性鱼鳞病(表皮松解性角化过度症)中的表达。
Br J Dermatol. 1994 Dec;131(6):767-79. doi: 10.1111/j.1365-2133.1994.tb08578.x.
7
Avian sebokeratocytes and marine mammal lipokeratinocytes: structural, lipid biochemical, and functional considerations.鸟类皮脂腺角质形成细胞和海洋哺乳动物脂角质形成细胞:结构、脂质生物化学及功能方面的考量
Am J Anat. 1987 Oct;180(2):161-77. doi: 10.1002/aja.1001800206.
8
Human epidermal glucosylceramides are major precursors of stratum corneum ceramides.人表皮葡糖神经酰胺是角质层神经酰胺的主要前体。
J Invest Dermatol. 2002 Aug;119(2):416-23. doi: 10.1046/j.1523-1747.2002.01836.x.
9
Comparison of rat epidermal keratinocyte organotypic culture (ROC) with intact human skin: lipid composition and thermal phase behavior of the stratum corneum.大鼠表皮角质形成细胞器官型培养(ROC)与完整人体皮肤的比较:角质层的脂质组成和热相行为
Biochim Biophys Acta. 2008 Apr;1778(4):824-34. doi: 10.1016/j.bbamem.2007.12.019. Epub 2008 Jan 4.
10
Vitamin C enhances differentiation of a continuous keratinocyte cell line (REK) into epidermis with normal stratum corneum ultrastructure and functional permeability barrier.维生素C可促进连续角质形成细胞系(REK)分化为具有正常角质层超微结构和功能性渗透屏障的表皮。
Histochem Cell Biol. 2001 Oct;116(4):287-97. doi: 10.1007/s004180100312.

引用本文的文献

1
The role of epidermal sphingolipids in dermatologic diseases.表皮鞘脂类在皮肤病中的作用。
Lipids Health Dis. 2016 Jan 19;15:13. doi: 10.1186/s12944-016-0178-7.
2
Effects of in utero exposure of C57BL/6J mice to 2,3,7,8-tetrachlorodibenzo-p-dioxin on epidermal permeability barrier development and function.子宫内暴露于2,3,7,8-四氯二苯并对二恶英对C57BL/6J小鼠表皮渗透屏障发育和功能的影响。
Environ Health Perspect. 2014 Oct;122(10):1052-8. doi: 10.1289/ehp.1308045. Epub 2014 Jun 6.
3
Two- and three-dimensional culture of keratinocyte stem and precursor cells derived from primary murine epidermal cultures.
从原代鼠表皮培养物中分离的角蛋白干细胞和前体细胞的二维和三维培养。
Stem Cell Rev Rep. 2012 Jun;8(2):402-13. doi: 10.1007/s12015-011-9314-y.
4
Highly efficient zinc-finger nuclease-mediated disruption of an eGFP transgene in keratinocyte stem cells without impairment of stem cell properties.高效锌指核酸酶介导的角质细胞干细胞中 eGFP 转基因的敲除而不损害干细胞特性。
Stem Cell Rev Rep. 2012 Jun;8(2):426-34. doi: 10.1007/s12015-011-9313-z.
5
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.角蛋白5基因的功能丧失突变会导致道林-迪戈斯病。
Am J Hum Genet. 2006 Mar;78(3):510-9. doi: 10.1086/500850. Epub 2006 Jan 19.
6
Epidermolysis bullosa simplex-type mutations alter the dynamics of the keratin cytoskeleton and reveal a contribution of actin to the transport of keratin subunits.单纯型大疱性表皮松解症相关突变改变了角蛋白细胞骨架的动力学,并揭示了肌动蛋白对角蛋白亚基运输的作用。
Mol Biol Cell. 2004 Mar;15(3):990-1002. doi: 10.1091/mbc.e03-09-0687. Epub 2003 Dec 10.
7
Formation of a normal epidermis supported by increased stability of keratins 5 and 14 in keratin 10 null mice.在角蛋白10基因敲除小鼠中,角蛋白5和14稳定性增加支持正常表皮形成。
Mol Biol Cell. 2001 Jun;12(6):1557-68. doi: 10.1091/mbc.12.6.1557.