Topographic Organization of the Peripheral Projections of the Trigeminal Ganglion in the Fetal Rat

References

• Arvidsson J. Somatotopic organization of vi-brissae afferents in the trigeminal sensory nuclei of the rat studied by transganglionic transport of HRP. J. Comp. Neurol. 1982; 211: 84–92
   PubMed Web of Science ®Google Scholar
• Bennett M., Ho S., Lavidis N. Competition between segmental nerves at end-plastes in rat gastrocnemius muscle during loss of polyneuronal innervation. J. Physiol. 1986; 381: 351–376
   PubMed Web of Science ®Google Scholar
• Betz J. H., Caldwell J. H., Ribchester R. R. The effects of partial denervation at birth on the development of muscle fibres and motor units in rat lubrical muscle. J. Physiol. 1980; 303: 265–279
   PubMed Web of Science ®Google Scholar
• Blakemore C., Garey L. J., Henderson Z., Swindale N. V., Vital-Durand F. Visual experience can promote rapid axonal reinnervation in monkey visual cortex. J. Physiol. 1980; 307: 25–26
   Web of Science ®Google Scholar
• Carr V. M., Simpson S. B., Jr. Proliferative and degenerative events in the early development of chick dorsal root ganglia: I. Normal development. J. Comp. Neurol. 1978; 182: 727–740
   PubMed Web of Science ®Google Scholar
• Chalupa L. M., Killackey H. P. Process elimination underlies ontogenetic change in the distribution of callosal projection neurons in the postcentral gyrus of the fetal rhesus monkey. Proc. Natl. Acad. Sci. USA 1989; 86: 1076–1079
   PubMed Web of Science ®Google Scholar
• Chiaia N. L., Allen Z., Carlson E., MacDonald G., Rhoades R. W. Neonatal infraorbital nerve transection in rat results in peripheral trigeminal sprouting. J. Comp. Neurol. 1988; 274: 101–114
   PubMed Web of Science ®Google Scholar
• Chiaia N. L., Hess P. R., Rhoades R. W. Preventing regeneration of infraorbital axons does not alter the ganglionic or transganglionic consequences of neonatal transection of this trigeminal branch. Dev. Brain Res. 1987; 36: 75–88
   Google Scholar
• Chiaia N. L., Macdonald G. J., Rhoades R. W. Effect of fetal infraorbital nerve transection upon the peripheral and central projections of individual trigeminal ganglion cells. Soc. Neurosci. Abstr. 1989; 15: 92
   Google Scholar
• Coimbra A., Ribeiro-Da-Silva A., Pignatelli D. Rexed's laminae and the acid phosphatase (FRAP)-band in the superficial dorsal horn of the neonatal rat spinal cord. Neurosci. Lett. 1986; 71: 131–136
   PubMed Web of Science ®Google Scholar
• Crissman R. S., Bennett-Clarke C., Chiaia N. L., Rhoades R. W. Central projections of trigeminal primary afferents in perinatal rats visualized by anterograde transport of Di-I. Soc. Neurosci. Abstr. 1989; 15: 843
   Google Scholar
• Davies A. M., Lumsden A. G. S. Relation of target encounter and neuronal death to nerve growth factor responsiveness in the developing mouse trigeminal ganglion. J. Comp. Neurol. 1984; 223: 124–137
   PubMed Web of Science ®Google Scholar
• Davies A. M., Lumsden A. G. S. Fasciculation in the early mouse trigeminal nerve is not ordered in relation to the emerging pattern of whisker follicles. J. Comp. Neurol. 1986; 253: 13–24
   PubMed Web of Science ®Google Scholar
• English K. B., Burgess P. R., Kavka-Van Normal D. Development of rat Merkel cells. J. Comp. Neurol. 1980; 194: 475–496
   PubMed Web of Science ®Google Scholar
• Erzurumlu R. S., Killackey H. P. Order in the developing rat trigeminal nerve. Dev. Brain Res. 1982; 3: 305–310
   Google Scholar
• Erzurumlu R. S., Killackey H. P. Development of order in the rat trigeminal system. J. Comp. Neurol. 1983; 213: 365–380
   PubMed Web of Science ®Google Scholar
• Fawcett J. W., O'Leary D. D. M., Cowan W. M. Activity and the control of ganglion cell death in the rat retina. Proc. Natl. Acad. Sci. USA 1984; 81: 5589–5593
   PubMed Web of Science ®Google Scholar
• Fish S. E., Rhoades R. W. A method for making very small, quantifiable micropipette injections of axonal tracer substances. J. Neurosci. Meth. 1981; 4: 291–297
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. The post-natal development of cutaneous afferent fiber input and receptive field organization in the rat dorsal horn. J. Physiol. 1985a; 364: 1–18
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. The sprouting of saphenous nerve terminals in the spinal cord following early postnatal sciatic nerve section in the rat. J. Comp. Neurol. 1985b; 240: 407–413
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. Spontaneous and evoked activity of fetal primary afferents in vivo. Nature 1987a; 326: 603
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. Cutaneous primary afferent properties in the hind limb of the neonatal rat. J. Physiol. 1987b; 383: 79–92
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. Prenatal growth of fine-diameter primary afferents into the rat spinal cord: A transganglionic tracer study. J. Comp. Neurol. 1987c; 261: 98–104
   PubMed Web of Science ®Google Scholar
• Fitzgerald M., Swett J. The termination pattern of sciatic nerve afferents in the substantia gelatinosa of neonatal rats. Neurosci. Lett. 1983; 43: 149–154
   PubMed Web of Science ®Google Scholar
• Fitzgerald M., Vrbova G. Plasticity of acid phosphatase (FRAP) afferent terminal fields and of dorsal horn cell growth in the neonatal rat. J. Comp. Neurol. 1985; 240: 414–422
   PubMed Web of Science ®Google Scholar
• Forbes D. J., Welt C. Neurogenesis in the trigeminal ganglion of the albino rat: A quantitative autoradiographic study. J. Comp. Neurol. 1981; 199: 133–147
   PubMed Web of Science ®Google Scholar
• Frank E., Westerfield M. Development of sensory-motor synapses in the spinal cord of the frog. J. Physiol. 1983; 343: 593–610
   PubMed Web of Science ®Google Scholar
• Gregg J. M., Dixon A. D. Somatotopic organization of the trigeminal ganglion in the rat. Arch. Oral Biol. 1973; 18: 487–498
   PubMed Web of Science ®Google Scholar
• Guillery R. W. Experiments to determine whether retinogeniculate axons can form translaminar collateral sprouts in the lateral geniculate nucleus of the cat. J. Comp. Neurol. 1972; 146: 407–420
   PubMed Web of Science ®Google Scholar
• Hamburger V., Levi-Montalcini R. Proliferation, differentiation, and degeneration in the spinal ganglia of the chick embryo under normal and experimental conditions. J. Exp. Zool. 1949; 111: 457–500
   PubMedGoogle Scholar
• Honig M. G. The development of sensory projection patterns in embryonic chick hind limb. J. Physiol. 1982; 330: 175–302
   PubMed Web of Science ®Google Scholar
• Hubel D. H., Wiesel T. N., LeVay S. Plasticity of ocular dominance columns in monkey striate cortex. Phil. Trans. Roy. Soc. B 1977; 278: 377–409
   PubMed Web of Science ®Google Scholar
• Innocenti G. M. Growth and reshaping of axons in the establishment of visual callosal connections. Science 1981; 212: 824–827
   PubMed Web of Science ®Google Scholar
• Ivy G. O., Killackey H. P. Ontogenetic changes in the projections of neocortical neurons. J. Neurosci. 1982; 2: 735–743
   PubMed Web of Science ®Google Scholar
• Jackson P. C., Diamond J. Failure of intact cutaneous mechanosensory axons to sprout functional collaterals in skin of adult rabbit. Brain Res. 1983; 273: 277–283
   PubMed Web of Science ®Google Scholar
• Jackson P. C., Diamond J. Temporal and spatial constraints on the collateral sprouting of low-threshold mechanosensory nerves in the skin of rats. J. Comp. Neurol. 1984; 226: 336–345
   PubMedGoogle Scholar
• Jacquin M. E., Renehan W. E., Klein B. G., Mooney R. D., Rhoades R. W. Functional consequences of neonatal infraorbital nerve section in rat trigeminal ganglion. J. Neurosci. 1986; 6: 3706–3720
   PubMed Web of Science ®Google Scholar
• Jacquin M. F., Rhoades R. W. Effects of neonatal infraorbital lesions upon central trigeminal primary afferent projections in rat and hamster. J. Comp. Neurol. 1985; 235: 129–143
   PubMed Web of Science ®Google Scholar
• Jacquin M. F., Semba K., Egger M. D., Rhoades R. W. Organization of HRP-labeled trigeminal mandibular primary afferent neurons in the rat. J. Comp. Neurol. 1983; 215: 397–420
   PubMed Web of Science ®Google Scholar
• Jacquin M. F., Semba K., Egger M. D., Rhoades R. W. Organization of HRP-labeled trigeminal mandibular primary afferent neurons in the rat. J. Comp. Neurol. 1983; 215: 397–420
   PubMed Web of Science ®Google Scholar
• Jacquin M. F., Semba K., Rhoades R. W., Egger M. D. Trigeminal primary afferents project bilaterally to dorsal horn and ipsilaterally to cerebellum, reticular formation and cuneate, solitary, supratrigeminal and vagal nuclei. Brain Res. 1982; 246: 285–291
   PubMed Web of Science ®Google Scholar
• Killackey H. P., Shinder A. Central correlates of peripheral pattern alterations in the trigeminal system of the rat: II. The effect of nerve section. Dev. Brain Res. 1981; 1: 121–126
   Google Scholar
• Klein B. G., Macdonald G. J., Szczepanik A. M., Rhoades R. W. Topographic organization of peripheral trigeminal ganglionic projections in newborn rats. Dev. Brain Res. 1986; 27: 257–262
   Google Scholar
• Klein B. G., Renehan W. E., Jacquin M. E., Rhoades R. W. Anatomical consequences of neonatal infraorbital nerve transection upon the trigeminal ganglion and vibrissa follicle nerves in the adult rat. J. Comp. Neurol. 1988; 268: 459–488
   Web of Science ®Google Scholar
• Kudo N., Yamada T. Morphological and physiological studies of development of the monosynaptic reflex pathway in the rat lumbar spinal cord. J. Physiol. 1987; 389: 441–459
   PubMed Web of Science ®Google Scholar
• Lance-Jones C. Motoneuron axon guidance: Development of specific projections to two muscles in the embryonic chick limb. Brain Behav. Evol. 1988; 31: 209–217
   PubMed Web of Science ®Google Scholar
• Lance-Jones C., Landmesser L. Motoneuron projection patterns to the chick hind limb following early partial reversals of the spinal cord. J. Physiol. 1980; 302: 581–602
   PubMed Web of Science ®Google Scholar
• Land P. W., Lund R. D. Development of rat's uncrossed retinotectal pathway and its relation to plasticity studies. Science 1979; 205: 698–700
   PubMed Web of Science ®Google Scholar
• Landmesser L., Morris D. G. The development of functional innervation in the hind limb of the chick embryo. J. Physiol. 1975; 249: 301–326
   PubMed Web of Science ®Google Scholar
• LeVay S., Stryker M. P., Shatz C. J. Ocular dominance columns and their development in layer IV of the cat's visual cortex: A quantitative study. J. Comp. Neurol. 1978; 179: 223–244
   PubMed Web of Science ®Google Scholar
• LeVay S., Wiesel T. N., Hubel D. H. The development of ocular dominance columns in normal and visually deprived monkeys. J. Comp. Neurol. 1980; 191: 1–51
   PubMed Web of Science ®Google Scholar
• Lumsden A. G. S., Davies A. M. Earliest sensory nerve fibers are guided by attractants other than nerve growth factor. Nature 1983; 306: 786–788
   PubMed Web of Science ®Google Scholar
• Myers P. Z., Eisen J. S., Westerfield M. Development and axonal outgrowth of identified motoneurons in the zebrafish. J. Neurosci. 1986; 6: 2278–2289
   PubMed Web of Science ®Google Scholar
• Noden D. M. Somatotopic organization of the embryonic chick trigeminal ganglion. J. Comp. Neurol. 1980; 190: 429–444
   PubMed Web of Science ®Google Scholar
• O'Leary D. D. M., Stanfield B. B., Cowan W. M. Evidence that the early postnatal restriction of the cells of origin of the callosal projection is due to the elimination of axonal collaterals rather than to the death of neurons. Dev. Brain Res. 1981; 1: 607–617
   Google Scholar
• O'Leary D. D. M., Terashima T. Cortical axons branch to multiple subcortical targets by interstitial axon budding: Implications for target recognition and “waiting periods”. Neuron 1988; 1: 901–910
   PubMed Web of Science ®Google Scholar
• Oppenheim R. W. Neuronal cell death and some related regressive phenomena during neurogenesis: A selective historical review and progress report. Studies in Developmental Neurobiology: Essays in Honor of Viktor Hamburger, W. M. Cowan. Oxford University Press, New York 1981; 74–133
   Google Scholar
• Rakic P., Riley K. Regulation of axon number in primate optic nerve by prenatal binocular competition. Nature 1983; 305: 135–137
   PubMed Web of Science ®Google Scholar
• Renehan W. E., Rhoades R. W. A quantitative electron microscopic analysis of the infraorbital newborn rat. Brain Res. 1984; 322: 369–373
   PubMed Web of Science ®Google Scholar
• Rhoades R. W., Chiaia N. L., Macdonald G. J., Jacquin M. E. The effect of fetal infraorbital nerve transection upon trigeminal primary afferent projections in the rat. J. Comp. Neurol. 1989; 287: 82–97
   PubMed Web of Science ®Google Scholar
• Rhoades R. W., Chiaia N. L., Mooney R. D., Klein B. G., Renehan W. E., Jacquin M. F. Reorganization of the peripheral projections of the trigeminal ganglion following neonatal transection of the infraorbital nerve. Somatosens. Res. 1987; 5: 35–62
   PubMed Web of Science ®Google Scholar
• Rhoades R. W., Fiore J. M., Math M. F., Jacquin M. F. Reorganization of trigeminal primary afferents following neonatal infraorbital nerve section in hamster. Dev. Brain Res. 1983; 7: 337–343
   Google Scholar
• Saito K. Development of spinal reflexes in the rat fetus studied in vitro. J. Physiol. 1979; 294: 581–594
   PubMed Web of Science ®Google Scholar
• Shatz C. J. The prenatal development of the cat's retinogeniculate pathway. J. Neurosci. 1983; 3: 482–499
   PubMed Web of Science ®Google Scholar
• Scott S. A. The development of the segmental pattern of skin sensory innervation in embryonic chick hind limb. J. Physiol. 1982; 333: 203–220
   Google Scholar
• Scott S. A. The effects of neural crest deletions on the development of sensory innervation patterns in embryonic chick hind limb. J. Physiol. 1984; 352: 285–304
   PubMed Web of Science ®Google Scholar
• Smith C. L. The development and postnatal organization of primary afferent projections to the rat thoracic spinal cord. J. Comp. Neurol. 1983; 269: 96–108
   Google Scholar
• Smith C. L., Frank E. Specificity of sensory projections to the spinal cord during development in bullfrog. J. Comp. Neurol. 1988; 269: 96–108
   PubMed Web of Science ®Google Scholar
• Sretavan D. W., Shatz C. J. Prenatal development of cat retinogeniculate axon arbors in the absence of binocular interactions. J. Neurosci. 1986; 6: 990–1003
   PubMed Web of Science ®Google Scholar
• Tosney K. W., Landmesser L. T. Specificity of early motoneuron growth cone outgrowth in the chick embryo. J. Neurosci. 1985; 5: 2336–2344
   PubMed Web of Science ®Google Scholar
• Van der Loos H., Woolsey T. A. Somatosensory cortex: Structural alterations following early injury to sense organs. Science 1973; 179: 395–397
   PubMed Web of Science ®Google Scholar
• Welt C. Somatotopic organization of the rat trigeminal ganglion determined by horseradish peroxidase (HRP) mapping. Soc. Neurosci. Abstr. 1982; 8: 1023
   Google Scholar
• Wessels W. J. T., Feierabend H. K. P., Marani E. Development of the sensory innervation in the rat hindlimb. Soc. Neurosci. Abstr. 1988; 14: 422
   Google Scholar
• Williams R. W., Chalupa L. M. Prenatal development of retinocollicular projections in the cat: An anterograde tracer transport study. J. Neurosci. 1982; 2: 604–622
   PubMed Web of Science ®Google Scholar