An investigation into the composition of amniotic membrane used for ocular surface reconstruction

被引:42
作者
Cooper, LJ
Kinoshita, S
German, M
Koizumi, N
Nakamura, T
Fullwood, NJ [1 ]
机构
[1] Univ Lancaster, Inst Environm & Nat Sci, Lancaster LA1 4YQ, England
[2] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kyoto, Japan
基金
英国惠康基金;
关键词
amniotic membrane; basal lamina; extracellular matrix;
D O I
10.1097/01.ico.0000154237.49112.29
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Cultivated limbal epithelial transplantation using an amniotic membrane (AM) carrier is now widely used for ocular surface reconstruction. The reasons for the exceptional success of AM as a carrier are not fully understood but are believed to be related to its unique composition. In this project we characterize, at the ultrastructural level, the extracellular matrix (ECM) components present in AM. We also compare the distribution of ECM components of cellular AM with that of denuded AM. Methods: Scanning, transmission, and atomic force microscopy was used to examine the structure of cellular and denuded amniotic membranes. Immunogold labeling with a panel of antibodies against ECM molecules was carried out on cellular and denuded AM. Results: Heparan sulfate, fibronectin, and laminin were present at high concentration in the lamina densa, Collagen IV was the major component of the basal lamina. Type I collagen was confined to the stroma along with significant amounts of keratan and chondroitin sulfate. Both cellular and denuded AMs had similar distributions of the ECM components. Conclusions: We were able to determine the distribution of ECM molecules in the lamina densa, basal lamina, and stroma of AM at the ultrastructural level. The removal of amniotic epithelial cells using our protocol does not appear to have any significant effects on the structure of the basal lamina or the distribution of ECM components.
引用
收藏
页码:722 / 729
页数:8
相关论文
共 25 条
  • [1] An ultrastructural investigation into proteoglycan distribution in human corneas
    Bairaktaris, G
    Lewis, D
    Fullwood, NJ
    Nieduszynski, IA
    Marcyniuk, B
    Quantock, AJ
    Ridgway, AEA
    [J]. CORNEA, 1998, 17 (04) : 396 - 402
  • [2] BEESLEY JE, 1989, MICROSCOPY HDB ROYAL, V17
  • [3] Amniotic membrane transplantation for severe neurotrophic corneal ulcers
    Chen, HJ
    Pires, RTF
    Tseng, SCG
    [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 2000, 84 (08) : 826 - 833
  • [4] An investigation of removed cultivated epithelial transplants in patients after allocultivated corneal epithelial transplantation
    Cooper, LJ
    Fullwood, NJ
    Koizumi, N
    Nakamura, T
    Kinoshita, S
    [J]. CORNEA, 2004, 23 (03) : 235 - 242
  • [5] Differential distribution of subchains of the basement membrane components type IV collagen and laminin among the amniotic membrane, cornea, and conjunctiva
    Fukuda, K
    Chikama, T
    Nakamura, M
    Nishida, T
    [J]. CORNEA, 1999, 18 (01) : 73 - 79
  • [6] Grueterich M, 2002, INVEST OPHTH VIS SCI, V43, P63
  • [7] Koizumi N, 2000, INVEST OPHTH VIS SCI, V41, P2506
  • [8] Cryopreserved human amniotic membrane for ocular surface reconstruction
    Kruse, FE
    Joussen, AM
    Rohrschneider, K
    You, LT
    Sinn, B
    Baumann, J
    Völcker, HE
    [J]. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2000, 238 (01) : 68 - 75
  • [9] Amniotic membrane transplantation for persistent epithelial defects with ulceration
    Lee, SH
    Tseng, SCG
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1997, 123 (03) : 303 - 312
  • [10] Corneal and scleral collagens - a microscopist's perspective
    Meek, KM
    Fullwood, NJ
    [J]. MICRON, 2001, 32 (03) : 261 - 272