Lim1 is essential for the correct Laminar positioning of retinal horizontal cells

被引:83
作者
Poche, Ross A. [1 ]
Kwan, Kin Ming [2 ]
Raven, Mary A. [4 ]
Furuta, Yasuhide [3 ]
Reese, Benjamin E. [4 ,5 ]
Behringer, Richard R. [1 ,2 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Program Dev Biol, Baylor Coll Med, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[4] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[5] Univ Calif Santa Barbara, Dept Psychol, Santa Barbara, CA 93106 USA
关键词
differentiation; horizontal cell; lamina; migration; plasticity; retina;
D O I
10.1523/JNEUROSCI.4046-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although much is known about the transcriptional regulation that coordinates retinal cell fate determination, very little is known about the developmental processes that establish the characteristic laminar architecture of the retina, in particular, the specification of neuronal positioning. The LIM class homeodomain transcription factor Lim1 (Lhx1) is expressed in postmitotic, differentiating, and mature retinal horizontal cells. We show that conditional ablation of Lim1 results in the ectopic localization of horizontal cells to inner aspects of the inner nuclear layer, among the retinal amacrine cells. The ectopic cells maintain a molecular phenotype consistent with horizontal cell identity; however, these neurons adopt a unique morphology more reminiscent of amacrine cells, including a dendritic arbor positioned within the inner plexiform layer. All other retinal cell populations appear unaltered. Our data suggest a model whereby Lim1 lies downstream of horizontal cell fate determination factors and functions cell autonomously to instruct differentiating horizontal cells to the appropriate laminar position in the developing retina. This study is the first to describe a cell type-specific genetic program that is essential for targeting a discrete retinal neuron population to the proper lamina.
引用
收藏
页码:14099 / 14107
页数:9
相关论文
共 43 条
  • [1] Interkinetic nuclear migration and the selection of neurogenic cell divisions during vertebrate retinogenesis
    Baye, Lisa M.
    Link, Brian A.
    [J]. JOURNAL OF NEUROSCIENCE, 2007, 27 (38) : 10143 - 10152
  • [2] BAYE LM, 2007, IN PRESS BRAIN RES
  • [3] Cell fate determination in the vertebrate retina
    Cepko, CL
    Austin, CP
    Yang, XJ
    Alexiades, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) : 589 - 595
  • [4] The roles of intrinsic and extrinsic cues and bHLH genes in the determination of retinal cell fates
    Cepko, CL
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (01) : 37 - 46
  • [5] Prox1 function controls progenitor cell proliferation and horizontal, cell genesis in the mammalian retina
    Dyer, MA
    Livesey, FJ
    Cepko, CL
    Oliver, G
    [J]. NATURE GENETICS, 2003, 34 (01) : 53 - 58
  • [6] Newborn horizontal cells migrate bi-directionally across the neuroepithelium during retinal development
    Edqvist, PHD
    Hallböök, F
    [J]. DEVELOPMENT, 2004, 131 (06): : 1343 - 1351
  • [7] FU X, 2003, DEV BIOL, V299, P424
  • [8] Ptf1a determines horizontal and amacrine cell fates during mouse retinal development
    Fujitani, Yoshio
    Fujitani, Shuko
    Luo, Huijun
    Qiu, Feng
    Burlison, Jared
    Long, Qiaoming
    Kawaguchi, Yoshiya
    Edlund, Helena
    MacDonald, Raymond J.
    Furukawa, Takahisa
    Fujikado, Takashi
    Magnuson, Mark A.
    Xiang, Mengqing
    Wright, Christopher V. E.
    [J]. DEVELOPMENT, 2006, 133 (22): : 4439 - 4450
  • [9] Furuta Y, 2000, GENESIS, V26, P130, DOI 10.1002/(SICI)1526-968X(200002)26:2<130::AID-GENE9>3.0.CO
  • [10] 2-I