Onset and time course of apoptosis in the developing zebrafish retina

被引:74
作者
Biehlmaier, O
Neuhauss, SCF
Kohler, K
机构
[1] Univ Tubingen, Hosp Eye, D-72076 Tubingen, Germany
[2] Univ Zurich, ETH, Brain Res Inst, CH-8057 Zurich, Switzerland
关键词
retina; apoptosis; development; zebrafish; Danio rerio (Teleostei);
D O I
10.1007/s004410100447
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In mammalian development, apoptosis spreads over the retina in consecutive waves and induces a remarkable amount of cell loss. No evidence for such consecutive waves has been revealed in the fish retina so far. As the zebrafish is of growing importance as a model for retinal development and for degenerative retinal diseases, we examined the onset and time course of apoptosis in the developing zebrafish retina and in adult fish. We found that apoptosis peaked in the ganglion cell layer (GCL) and inner nuclear layer (INL) in early developmental stages (3-4 days post-fertilization; dpf) followed by a second, but clearly smaller wave at 6-7dpf. Apoptosis in the outer nuclear layer (ONL) started at 5dpf and peaked at 7dpf. This late-onset high peak of apoptosis of photoreceptors is different from that of all other species examined to date. With 1.09% of cells in the GCL and 1.10% in the ONL being apoptotic, the rate of apoptosis in the developing zebrafish retina was conspicuously lower than that observed in other vertebrates (up to 50% in GCL). During development (2-21dpf), apoptotic waves were most obvious in the central retina, whereas in the periphery near the marginal zone (MZ), apoptosis was much lower; in adult animals, practically no apoptosis was present in the central retina but it still occurred near the MZ. Our data show that the onset and time course of apoptosis in the GCL and INL of the zebrafish is comparable with other vertebrates; however, the amount of apoptosis is clearly reduced. Thus, apoptosis in the zebrafish retina may serve more as a mechanism for the fine tuning of the retinal neuronal network after mitotic waves during development or in remaining mitotic areas than as a mechanism for eliminating large numbers of excess cells.
引用
收藏
页码:199 / 207
页数:9
相关论文
共 34 条
  • [1] Abdelilah S, 1996, DEVELOPMENT, V123, P217
  • [2] AN INVESTIGATION INTO THE ROLE OF GANGLION-CELLS IN THE REGULATION OF DIVISION AND DEATH OF OTHER RETINAL CELLS
    BEAZLEY, LD
    PERRY, VH
    BAKER, B
    DARBY, JE
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1987, 33 (02): : 169 - 184
  • [3] bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations
    Chen, J
    Flannery, JG
    LaVail, MM
    Steinberg, RH
    Xu, J
    Simon, MI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) : 7042 - 7047
  • [4] Cook B, 1998, J COMP NEUROL, V396, P12, DOI 10.1002/(SICI)1096-9861(19980622)396:1<12::AID-CNE2>3.0.CO
  • [5] 2-L
  • [6] Daly FJ, 2000, ANAT RECORD, V258, P145
  • [7] FurutaniSeiki M, 1996, DEVELOPMENT, V123, P229
  • [8] IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION
    GAVRIELI, Y
    SHERMAN, Y
    BENSASSON, SA
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 119 (03) : 493 - 501
  • [9] GLUCKSMANN A., 1940, BRIT JOUR OPHTHALMOL, V24, P153, DOI 10.1136/bjo.24.4.153
  • [10] Mutations affecting pigmentation and shape of the adult zebrafish
    Haffter, P
    Odenthal, J
    Mullins, MC
    Lin, S
    Farrell, MJ
    Vogelsang, E
    Haas, F
    Brand, M
    vanEeden, FJM
    FurutaniSeiki, M
    Granato, M
    Hammerschmidt, M
    Heisenberg, CP
    Jiang, YJ
    Kane, DA
    Kelsh, RN
    Hopkins, N
    NussleinVolhard, C
    [J]. DEVELOPMENT GENES AND EVOLUTION, 1996, 206 (04) : 260 - 276