Complex organization of mouse and rat suprachiasmatic nucleus

The suprachiasmatic nucleus, site of the dominant mammalian circadian clock, contains a variety of different neurons that tend to form groups within the nucleus. The present investigation used single and multiple label tract tracing and immunofluorescence methods to evaluate the relative locations of the neuron groups and to compare them with the distributions of the three major afferent projections, the retinohypothalamic tract, geniculohypothalamic tract and the serotonergic pathway from the median raphe nucleus. The suprachiasmatic nucleus has a complex order characterized by peptidergic cell groups (vasopressin, gastrin releasing peptide, vasoactive intestinal polypeptide, calbindin, calretinin, corticotrophin releasing factor and enkephalin) that, in most cases, substantially overlap. The retinohypothalamic tract projects bilaterally to virtually all the suprachiasmatic nucleus in both rat (predominantly contralateral) and mouse (symmetric) and its terminal field overlaps that for the geniculohypothalamic tract, but with distinctions visible according to density criteria; neither provides more than sparse innervation of the dorsomedial suprachiasmatic nucleus. In the mouse, the serotonergic terminal field is densest medially and ventrally, but is also distributed elsewhere with varying density. The serotonergic terminal plexus in the rat is densest centromedially and largely, but not completely, overlaps the complete distribution of retinal terminals with density much reduced in the lateral suprachiasmatic nucleus. The locations of vasopressin neurons, retinohypothalamic tract terminals and serotonergic (mouse, rat) or geniculohypothalamic tract (rat) provide evidence for three clear, but not exclusionary, sectors of the suprachiasmatic nucleus. The data, in conjunction with emerging knowledge concerning rhythmically dynamic changes in the size of regions of neuropeptide gene expression in suprachiasmatic nucleus cells, support the view that suprachiasmatic nucleus organization is more complex than a simple "core" and "shell" arrangement. While generalizations about suprachiasmatic nucleus organization can be made with respect to location of cell phenotypes or terminal fields, oversimplification may hinder, rather than facilitate, understanding of suprachiasmatic nucleus structure-function relationships.

[1]  W. Rietveld,et al.  Vasopressin-deficient suprachiasmatic nucleus grafts re-instate circadian rhythmicity in suprachiasmatic nucleus-lesioned arrhythmic rats , 1999, Neuroscience.

[2]  H. Rodman,et al.  Pattern of retinal projections in the California ground squirrel (Spermophilus beecheyi): Anterograde tracing study using cholera toxin , 2003, The Journal of comparative neurology.

[3]  R. Moore,et al.  Entrainment pathways and the functional organization of the circadian system. , 1996, Progress in brain research.

[4]  Lance J. Kriegsfeld,et al.  Targeted Microlesions Reveal Novel Organization of the Hamster Suprachiasmatic Nucleus , 2004, The Journal of Neuroscience.

[5]  L. P. Morin,et al.  Retinohypothalamic projections in the hamster and rat demonstrated using cholera toxin , 1988, Brain Research.

[6]  R. Silver,et al.  Calbindin Influences Response to Photic Input in Suprachiasmatic Nucleus , 2003, The Journal of Neuroscience.

[7]  R. Leak,et al.  Suprachiasmatic pacemaker organization analyzed by viral transynaptic transport , 1999, Brain Research.

[8]  L. P. Morin,et al.  Neuromodulator content of hamster intergeniculate leaflet neurons and their projection to the suprachiasmatic nucleus or visual midbrain , 2001, The Journal of comparative neurology.

[9]  L. P. Morin,et al.  The circadian visual system, 2005 , 2006, Brain Research Reviews.

[10]  J. Meijer,et al.  Phase differences in electrical discharge rhythms between neuronal populations of the left and right suprachiasmatic nuclei , 2001, Neuroscience.

[11]  L. Kriegsfeld,et al.  Signaling within the Master Clock of the Brain: Localized Activation of Mitogen-Activated Protein Kinase by Gastrin-Releasing Peptide , 2005, The Journal of Neuroscience.

[12]  Erik D Herzog,et al.  Vasoactive intestinal polypeptide mediates circadian rhythmicity and synchrony in mammalian clock neurons , 2005, Nature Neuroscience.

[13]  R. Silver,et al.  Temporal and spatial expression patterns of canonical clock genes and clock‐controlled genes in the suprachiasmatic nucleus , 2004, The European journal of neuroscience.

[14]  Yasufumi Shigeyoshi,et al.  An Abrupt Shift in the Day/Night Cycle Causes Desynchrony in the Mammalian Circadian Center , 2003, The Journal of Neuroscience.

[15]  D. Cutler,et al.  Distribution of substance P and neurokinin‐1 receptor immunoreactivity in the suprachiasmatic nuclei and intergeniculate leaflet of hamster, mouse, and rat , 2001, The Journal of comparative neurology.

[16]  I. Zucker,et al.  Circadian rhythms in drinking behavior and locomotor activity of rats are eliminated by hypothalamic lesions. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[17]  C. Pennartz,et al.  Hypothalamic integration of circadian rhythms , 1996 .

[18]  Rae Silver,et al.  Expression of Period Genes: Rhythmic and Nonrhythmic Compartments of the Suprachiasmatic Nucleus Pacemaker , 2001, The Journal of Neuroscience.

[19]  R. Moore,et al.  The suprachiasmatic nucleus of the golden hamster: Immunohistochemical analysis of cell and fiber distribution , 1984, Neuroscience.

[20]  R. Silver,et al.  Multiple regulatory elements result in regional specificity in circadian rhythms of neuropeptide expression in mouse SCN. , 1999, Neuroreport.

[21]  H. Okamura,et al.  Gradients in the circadian expression of Per1 and Per2 genes in the rat suprachiasmatic nucleus , 2002, The European journal of neuroscience.

[22]  S. Reuss,et al.  Substance P-like immunoreactivity in the hypothalamic suprachiasmatic nucleus of Phodopus sungorus — relation to daytime, photoperiod, sex and age , 1994, Brain Research.

[23]  R. Moore,et al.  Suprachiasmatic nucleus in the mouse: retinal innervation, intrinsic organization and efferent projections , 2001, Brain Research.

[24]  R. Moore,et al.  A retinohypothalamic projection in the rat , 1972, The Journal of comparative neurology.

[25]  F. Dudek,et al.  5-HT1B Receptor–Mediated Presynaptic Inhibition of Retinal Input to the Suprachiasmatic Nucleus , 1999, The Journal of Neuroscience.

[26]  M. Coculescu,et al.  Vasopressin neurotransmission and the control of circadian rhythms in the suprachiasmatic nucleus. , 1998, Progress in brain research.

[27]  R. Moore,et al.  Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. , 1972, Brain research.

[28]  L. Martinet,et al.  Neurons containing gastrin-releasing peptide and vasoactive intestinal polypeptide are involved in the reception of the photic signal in the suprachiasmatic nucleus of the Syrian hamster: an immunocytochemical ultrastructural study , 1998, Cell and Tissue Research.

[29]  L. P. Morin,et al.  Retinal ganglion cell projections to the hamster suprachiasmatic nucleus, intergeniculate leaflet, and visual midbrain: Bifurcation and melanopsin immunoreactivity , 2003, The Journal of comparative neurology.

[30]  F. Davis,et al.  Transplanted suprachiasmatic nucleus determines circadian period. , 1990, Science.

[31]  A. Hendrickson,et al.  An autoradiographic and electron microscopic study of retino-hypothalamic connections , 2004, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[32]  S. Kuhlman,et al.  GFP fluorescence reports Period 1 circadian gene regulation in the mammalian biological clock , 2000, Neuroreport.

[33]  P. Pévet,et al.  Per and neuropeptide expression in the rat suprachiasmatic nuclei: compartmentalization and differential cellular induction by light , 2002, Brain Research.

[34]  L. P. Morin,et al.  Immunocytochemical characterization of the suprachiasmatic nucleus and the intergeniculate leaflet in the diurnal ground squirrel, Spermophilus lateralis , 1991, Brain Research.

[35]  Sandra J. Kuhlman,et al.  The Biological Clock Nucleus: A Multiphasic Oscillator Network Regulated by Light , 2003, The Journal of Neuroscience.

[36]  R. Silver,et al.  Calbindin‐D28K cells in the hamster SCN express light‐induced Fos , 1996, Neuroreport.

[37]  V. Cassone,et al.  Comparative Anatomy of the Mammalian Hypothalamic Suprachiasmatic Nucleus , 1988, Journal of biological rhythms.

[38]  L. P. Morin The circadian visual system , 1994, Brain Research Reviews.

[39]  Rae Silver,et al.  The eye is necessary for a circadian rhythm in the suprachiasmatic nucleus , 2003, Nature Neuroscience.

[40]  L. Kriegsfeld,et al.  Calbindin-D28K cells selectively contact intra-SCN neurons , 2002, Neuroscience.

[41]  Y. Sagot,et al.  NGF‐induced motoneuron cell death depends on the genetic background and motoneuron sub‐type , 2000, Neuroreport.

[42]  R. Leak,et al.  Suprachiasmatic nucleus organization , 2002, Cell and Tissue Research.

[43]  R. Dyball,et al.  Defined Cell Groups in the Rat Suprachiasmatic Nucleus Have Different Day/Night Rhythms of Single-Unit Activity In Vivo , 2003, Journal of biological rhythms.

[44]  R. Moore,et al.  GABA is the principal neurotransmitter of the circadian system , 1993, Neuroscience Letters.

[45]  R. Gillette,et al.  Circadian rhythm of firing rate recorded from single cells in the rat suprachiasmatic brain slice , 1982, Brain Research.

[46]  L. Smale,et al.  Calbindin and Fos within the suprachiasmatic nucleus and the adjacent hypothalamus of Arvicanthis niloticus and Rattus norvegicus , 2000, Neuroscience.

[47]  S. Yamaguchi,et al.  Synchronization of Cellular Clocks in the Suprachiasmatic Nucleus , 2003, Science.

[48]  W. Schwartz,et al.  Light‐induced c‐Fos Expression in the Mouse Suprachiasmatic Nucleus: Immunoelectron Microscopy Reveals Co‐localization in Multiple Cell Types , 1997, The European journal of neuroscience.

[49]  R. Leak,et al.  Topographic organization of suprachiasmatic nucleus projection neurons , 2001, The Journal of comparative neurology.

[50]  R. Monnerie,et al.  Vasoactive Intestinal Polypeptide in the Suprachiasmatic Nucleus of the Mink (Mustela vison) Could Play a Key Role in Photic Induction , 1995, Journal of neuroendocrinology.

[51]  P. Tresco,et al.  A diffusible coupling signal from the transplanted suprachiasmatic nucleus controlling circadian locomotor rhythms , 1996, Nature.

[52]  J. D. Miller,et al.  New insights into the mammalian circadian clock. , 1996, Sleep.

[53]  Rae Silver,et al.  Localization of a Suprachiasmatic Nucleus Subregion Regulating Locomotor Rhythmicity , 1999, The Journal of Neuroscience.

[54]  C. Colwell,et al.  Disrupted circadian rhythms in VIP- and PHI-deficient mice. , 2003, American journal of physiology. Regulatory, integrative and comparative physiology.

[55]  R. Snowball,et al.  Circadian rhythm of neuronal activity in suprachiasmatic nucleus slices from the vasopressin-deficient Brattleboro rat , 1996, Neuroscience.

[56]  S. T. Inouye,et al.  Persistence of circadian rhythmicity in a mammalian hypothalamic "island" containing the suprachiasmatic nucleus. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[57]  L. Smale,et al.  Suprachiasmatic nucleus and intergeniculate leaflet in the diurnal rodent Octodon degus: retinal projections and immunocytochemical characterization , 1999, Neuroscience.

[58]  L. P. Morin,et al.  Intergeniculate leaflet and suprachiasmatic nucleus organization and connections in the golden hamster , 1992, Visual Neuroscience.

[59]  H. Okamura,et al.  Two types of VIP neuronal components in rat suprachiasmatic nucleus , 2003, Journal of neuroscience research.

[60]  Andrew D Huberman,et al.  Crossed and uncrossed retinal projections to the hamster circadian system , 2003, The Journal of comparative neurology.

[61]  Johanna H. Meijer,et al.  Heterogeneity of rhythmic suprachiasmatic nucleus neurons: Implications for circadian waveform and photoperiodic encoding , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[62]  C. Allen,et al.  Calbindin neurons in the hamster suprachiasmatic nucleus do not exhibit a circadian variation in spontaneous firing rate , 2002, The European journal of neuroscience.

[63]  Samer Hattar,et al.  Central projections of melanopsin‐expressing retinal ganglion cells in the mouse , 2006, The Journal of comparative neurology.