Apoptosis in developing retinal tissue

被引:97
作者
Linden, R [1 ]
Rehen, SK [1 ]
Chiarini, LB [1 ]
机构
[1] Univ Fed Rio de Janeiro, Ctr Ciencias Saude, Inst Biofis, BR-21949900 Rio de Janeiro, Brazil
关键词
D O I
10.1016/S1350-9462(98)00020-2
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The mechanisms of apoptosis are strongly dependent an cell-cell interactions typical of organized tissues. Experimental studies of apoptosis using a histotypical preparation of retinal explants are reported in the present article. We found that various characteristics or apoptosis are selectively associated with retinal cell death depending on cell type. stage: of maturation. aad means of induction of apoptosis. Among these were: (1) thr requirements of protein synthesis; (2) the role of cAMP: (5) the expression of certain apoptosis-associated proteins: and (3) the sensitivity to excitotoxicity. modulation of protein phosphatases and calcium mobilization. Dividing cells undergo apoptosis in response to several inducers in specific phases of the cell cycle, and in distinct regions within their pathway of interkinetic nuclear migration. Recent post-mitotic cells are selectively sensitive to apoptosis induced by blockade of protein synthesis. while both proliferating and differentiated cells are more resistant, We also studied the association of several proteins, some of which play critical roles in the cell cycle, with both differentiation anti apoptosis in the retinal tissue. Detection of ct II cycle markers did not support thr hypothesis that retinal cells re-enter the cell cycle on their pathway to apoptosis although some proteins associated with cell proliferation re-appeared ill degenerating cells. The transcription factors c-Jun, c-Fos and c-Myc were found associated and apoptosis in retinal cells. but their sub-cellular location In apoptotic bodies is not consistent with their canonical functions in the control of gene expression. The bifunctional redox factor/AP endonuclease Ref-1 and the transcription factor Max are associated with progressive cell differentiation, and both ate down-regulated during ct-Il death in the retina. The data suggest that Ref-1 and Max may normally function as negative modulators of retinal apoptosis, The results indicate that nuclear exclusion of transcription factors and other important control proteins is a hallmark of retinal apoptosis. Histotypical explants mag. be a choice preparation for the experimental analysis of the mechanisms or. apoptosis. in the context both or. cell-cell interactions and of. the dynamic behavior of uf developing cells within the organized retinal tissue. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:133 / 165
页数:33
相关论文
共 262 条
[81]  
HAIMOVITZFRIEDMAN A, 1994, CANCER RES, V54, P2591
[82]  
Hallbook F, 1996, J COMP NEUROL, V364, P664
[83]   A C-JUN DOMINANT-NEGATIVE MUTANT PROTECTS SYMPATHETIC NEURONS AGAINST PROGRAMMED CELL-DEATH [J].
HAM, J ;
BABIJ, C ;
WHITFIELD, J ;
PFARR, CM ;
LALLEMAND, D ;
YANIV, M ;
RUBIN, LL .
NEURON, 1995, 14 (05) :927-939
[84]   NERVE GROWTH-FACTOR PREVENTS BOTH NEURORETINAL PROGRAMMED CELL-DEATH AND CAPILLARY PATHOLOGY IN EXPERIMENTAL DIABETES [J].
HAMMES, HP ;
FEDEROFF, HJ ;
BROWNLEE, M .
MOLECULAR MEDICINE, 1995, 1 (05) :527-534
[85]  
HAN JH, 1995, EXP HEMATOL, V23, P265
[86]   p53; From inductive signal to cellular effect [J].
Hansen, R ;
Oren, M .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (01) :46-51
[87]   CELL-DEATH IN THE INNER AND OUTER NUCLEAR LAYERS OF THE DEVELOPING RETINA IN THE WALLABY SETONIX-BRACHYURUS (QUOKKA) [J].
HARMAN, AM ;
SNELL, LL ;
BEAZLEY, LD .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 289 (01) :1-10
[88]   GDNF - A POTENT SURVIVAL FACTOR FOR MOTONEURONS PRESENT IN PERIPHERAL-NERVE AND MUSCLE [J].
HENDERSON, CE ;
PHILLIPS, HS ;
POLLOCK, RA ;
DAVIES, AM ;
LEMEULLE, C ;
ARMANINI, M ;
SIMPSON, LC ;
MOFFET, B ;
VANDLEN, RA ;
KOLIATSOS, VE ;
ROSENTHAL, A .
SCIENCE, 1994, 266 (5187) :1062-1064
[89]   DIFFERENT RHODOPSIN MONOCLONAL-ANTIBODIES REVEAL DIFFERENT BINDING PATTERNS ON DEVELOPING AND ADULT-RAT RETINA [J].
HICKS, D ;
BARNSTABLE, CJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1987, 35 (11) :1317-1328
[90]  
HOPEWELL R, 1995, MOL CELL BIOL, V15, P3470