Human lens cells in culture.: I.: Isolation of adult lens epithelial cells from lens capsule preparations and reactivation of nucleus containing fiber cells

被引:3
|
作者
Iwig, M
Glässer, D
Luther, M
Struck, HG
机构
[1] Univ Halle Wittenberg, Fak Med, Inst Physiol Chem, D-06097 Halle, Germany
[2] Univ Halle Wittenberg, Klin & Poliklin Augenheilkunde, Arbeitsbereich Expt Ophthalmol, D-06097 Halle, Germany
关键词
lens epithelial cells; cell culturing; human lens cell lines; lens fiber cells; secondary cataract;
D O I
10.1055/s-2001-12253
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Bovine lens epithelial cells in culture revealed a high sensitivity against micromolar concentrations of linoleic acid. To prove the assumption that unsatturated free fatty acids are risk factors for cataractogenesis, human lens cell lines are needed. Furthermore, the reactivation of nucleus-containing fiber cells to mitotic growth may hint at their role in after cataract genesis. Material and methods: Epithelium-capsule-preparations obtained by capsulorhexis were cultured in serum containing medium. Subculturing of these adult human lens epithelial cells was done by trypsinization. Fiber cell bundles from the equator region of a fetal human lens were transfered into culture medium. Aggregates of nucleus containing fiber cells were isolated from floating fiber cell bundles by trypsinization. Subculturing and cryoconservation of suitable cell lines. Results: Primary culture of epithelium-capsule-preparations results in flattening, migration and proliferation of adult human lens epithelial cells. Nucleus containing fiber cells were reactivated to mitotic growth after adhesion to a suitable substratum. Established cell lines were received from adult human lens epithelial cells and fetal human fiber cells after repeated subculturing. Conclusions: Lens-capsule-preparations available from cataract surgery are well suited for the isolation of human lens cell lines, which were needed for testing cytotoxicity of drugs and for tracing of cataractogenic risk factors. The finding that nucleus containing fiber cells from the equator of human lenses can be reactivated to proliferating cells let us suppose, that these cells, which can not be removed easely from the posterior lens capsule, contribute to the after cataract formation.
引用
收藏
页码:102 / 110
页数:9
相关论文
共 50 条
  • [1] SYNTHESIS OF LENS CAPSULE IN LONG-TERM CULTURE OF HUMAN LENS EPITHELIAL-CELLS
    ARITA, T
    MURATA, Y
    LIN, LR
    TSUJI, T
    REDDY, VN
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1993, 34 (02) : 355 - 362
  • [2] Anterior lens capsule as a tool to study the physiology of human lens epithelial cells
    Andjelic, Sofija
    Zupancic, Gregor
    Perovsek, Darko
    Robic, Tatjana
    Hawlina, Marko
    ZDRAVNISKI VESTNIK-SLOVENIAN MEDICAL JOURNAL, 2010, 79 : 123 - 130
  • [3] PHYSIOLOGY OF HUMAN EPITHELIAL LENS CELLS IN CULTURE
    TASSIN, J
    COURTOIS, Y
    GERONTOLOGY, 1979, 25 (03) : 172 - 173
  • [4] Human anterior lens capsule epithelial cells contraction
    Andjelic, Sofija
    Zupancic, Gregor
    Perovsek, Darko
    Hawlina, Marko
    ACTA OPHTHALMOLOGICA, 2011, 89 (08) : e645 - e653
  • [5] Human sera obtained from patients with cataract killed lens epithelial cells in culture.
    Chylack, LT
    Singh, DP
    Kikuchi, T
    Sueno, T
    Wolfe, J
    Shinohara, T
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 5225 - 5225
  • [6] VOLUME REGULATION IN LENS EPITHELIAL-CELLS AND DIFFERENTIATING LENS FIBER CELLS
    BEEBE, DC
    PARMELEE, JT
    BELCHER, KS
    JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (03) : 455 - 459
  • [7] Expression of matrix metalloproteinases of human lens epithelial cells in the cultured lens capsule bag
    Li, J. H.
    Wang, N. L.
    Wang, J. J.
    EYE, 2008, 22 (03) : 439 - 444
  • [8] Expression of matrix metalloproteinases of human lens epithelial cells in the cultured lens capsule bag
    J H Li
    N L Wang
    J J Wang
    Eye, 2008, 22 : 439 - 444
  • [9] GROWTH OF HUMAN LENS EPITHELIAL-CELLS ON THE ANTERIOR LENS CAPSULE IN-VITRO
    MEYER, JH
    SCHMIDT, J
    EPPINGER, F
    FLUGEL, B
    LOFFLER, KU
    HANSEN, LL
    VISION RESEARCH, 1995, 35 : P229 - P229