Cellular circadian clocks in the pineal

被引:243
作者
Falcón, J [1 ]
机构
[1] Univ Poitiers, Lab Neurobiol Cellulaire, Dept Neurosci, CNRS UMR 6558, F-86022 Poitiers, France
关键词
D O I
10.1016/S0301-0082(98)00078-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Daily rhythms are a fundamental feature of all living organisms: most are synchronized by the 24 hr light/dark (LD) cycle. In most species, these rhythms are generated by a circadian system, and free run under constant conditions with a period close to 24 hr. To function properly the system needs a pacemaker or clock, an entrainment pathway to the clock, and one or more output signals, In vertebrates, the pineal hormone melatonin is one of these signals which functions as an internal time-keeping molecule. Its production is high at night and low during day. Evidence indicates that each melatonin producing cell of the pineal constitutes a circadian system pci sc in non-mammalian vertebrates. Ln addition to the melatonin generating system, they contain the clock as well as the photoreceptive unit. This is despite the fact that these cells have been profoundly modified from fish to birds. Modifications include a regression of the photoreceptive capacities, and of the ability to transmit a nervous message to the brain. The ultimate stage of this evolutionary process leads to the definitive loss of both the direct photosensitivity and the clock, as observed in the pineal of mammals. This review focuses on the functional properties of the cellular circadian clocks of non-mammalian vertebrates. How functions the clock? How is the photoreceptive unit linked to it and how is the clock linked to its output signal? These questions are addressed in light of past and recent data obtained in vertebrates, as well as invertebrates and unicellulars, (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:121 / 162
页数:42
相关论文
共 349 条
[1]   S-ANTIGEN FROM THE RAT RETINA AND PINEAL-GLAND HAVE IDENTICAL SEQUENCES [J].
ABE, T ;
SHINOHARA, T .
EXPERIMENTAL EYE RESEARCH, 1990, 51 (01) :111-112
[2]   A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light [J].
Albrecht, U ;
Sun, ZS ;
Eichele, G ;
Lee, CC .
CELL, 1997, 91 (07) :1055-1064
[3]   Functional identification of the mouse circadian Clock gene by transgenic BAC rescue [J].
Antoch, MP ;
Song, EJ ;
Chang, AM ;
Vitaterna, MH ;
Zhao, YL ;
Wilsbacher, LD ;
Sangoram, AM ;
King, DP ;
Pinto, LH ;
Takahashi, JS .
CELL, 1997, 89 (04) :655-667
[4]   DIFFERENTIATION OF BOTH ROD AND CONE TYPES OF PHOTORECEPTORS IN THE INVIVO AND INVITRO DEVELOPING PINEAL GLANDS OF THE QUAIL [J].
ARAKI, M ;
FUKADA, Y ;
SHICHIDA, Y ;
YOSHIZAWA, T ;
TOKUNAGA, F .
DEVELOPMENTAL BRAIN RESEARCH, 1992, 65 (01) :85-92
[5]   PHENOTYPIC-EXPRESSION OF PHOTORECEPTOR AND ENDOCRINE CELL PROPERTIES BY CULTURED PINEAL CELLS OF THE NEWBORN RAT [J].
ARAKI, M ;
WATANABE, K ;
TOKUNAGA, F ;
NONAKA, T .
CELL DIFFERENTIATION AND DEVELOPMENT, 1988, 25 (02) :155-164
[6]   NOREPINEPHRINE SUPPRESSES BOTH PHOTORECEPTOR AND NEURON-LIKE PROPERTIES EXPRESSED BY CULTURED RAT PINEAL GLANDS [J].
ARAKI, M ;
TOKUNAGA, F .
CELL DIFFERENTIATION AND DEVELOPMENT, 1990, 31 (02) :129-135
[7]   CELLULAR MECHANISM FOR NOREPINEPHRINE SUPPRESSION OF PINEAL PHOTORECEPTOR-LIKE CELL-DIFFERENTIATION IN RAT PINEAL CULTURES [J].
ARAKI, M .
DEVELOPMENTAL BIOLOGY, 1992, 149 (02) :440-447
[8]   Treatment of circadian rhythm disorders - Melatonin [J].
Arendt, J ;
Deacon, S .
CHRONOBIOLOGY INTERNATIONAL, 1997, 14 (02) :185-204
[9]   MELATONIN AND CIRCADIAN CONTROL IN MAMMALS [J].
ARMSTRONG, SM .
EXPERIENTIA, 1989, 45 (10) :932-938
[10]   NEGATIVE FEEDBACK DEFINING A CIRCADIAN CLOCK - AUTOREGULATION OF THE CLOCK GENE-FREQUENCY [J].
ARONSON, BD ;
JOHNSON, KA ;
LOROS, JJ ;
DUNLAP, JC .
SCIENCE, 1994, 263 (5153) :1578-1584