Fetal NGF augmentation preserves excess trigeminal ganglion cells and interrupts whisker-related pattern formation

In the developing nervous system, precisely patterned connections result from mechanisms that remodel initially diffuse connections. For example, ocular dominance column formation depends upon activity-based competitive interactions. In the developing trigeminal (V) somatosensory system, injury to afferent inputs prevents somatotopic pattern formation; however, afferent impulse blockade does not. What establishes central V patterns remains unclear. As a first step in assessing the role of neurotrophins in naturally occurring death of V ganglion cells and whisker-related pattern formation, the consequences of prenatal NGF injections were evaluated. Fetal rats given NGF on both embryonic day (E) 15 and E18 had 36% more V ganglion cells than normal and lacked whisker-related patterns in the V brainstem complex at birth and through postnatal day 3, as determined by cytochrome oxidase histochemistry. Rats injected with NGF on E16 or on E18, or with vehicle had normal ganglion cell numbers and brainstem patterns. Animals injected with antibodies to NGF or an NGF receptor had reduced ganglion cell numbers and normal brainstem patterns. These findings suggest that naturally occurring cell death in the V ganglion is neurotrophically regulated and that this process impacts upon somatotopic pattern formation in the V brainstem complex. Results of anterograde tracing experiments in NGF-augmented animals suggest that pattern disruptions are due to an absence of whisker-related patterning in the central projections of V ganglion cells. Moreover, single primary afferent collaterals labeled by Neurobiotin injections in the V ganglion did not have widespread or unusually complex arbors. Thus, NGF may affect V pattern formation by preserving or inducing projections to brainstem regions that normally come to lack such projections, such as the spaces normally demarcating neighboring whisker primary afferent projections.

[1]  R. W. Gundersen,et al.  Neuronal chemotaxis: chick dorsal-root axons turn toward high concentrations of nerve growth factor. , 1979, Science.

[2]  P. Distefano,et al.  Identification of a truncated form of the nerve growth factor receptor. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. van der Loos,et al.  Barreloids in mouse somatosensory thalamus. , 1976, Neuroscience letters.

[4]  Richard E. Coggeshall,et al.  A consideration of neural counting methods , 1992, Trends in Neurosciences.

[5]  M. Barbacid,et al.  trkC, a new member of the trk family of tyrosine protein kinases, is a receptor for neurotrophin-3 , 1991, Cell.

[6]  G. Burnstock,et al.  Influence of nerve growth factor on the embryonic mouse trigeminal ganglion in culture. , 1981, Developmental neuroscience.

[7]  A. Davies,et al.  Relation of target encounter and neuronal death to nerve growth factor responsiveness in the developing mouse trigeminal ganglion , 1984, The Journal of comparative neurology.

[8]  H. Thoenen,et al.  Purification of a new neurotrophic factor from mammalian brain. , 1982, The EMBO journal.

[9]  M. Jacquin,et al.  Development and plasticity in hamster trigeminal primary afferent projections. , 1987, Brain research.

[10]  M F Jacquin,et al.  Morphology and topography of identified primary afferents in trigeminal subnuclei principalis and oralis. , 1993, Journal of neurophysiology.

[11]  N. Chiaia,et al.  Normal development and effects of neonatal infraorbital nerve damage upon the innervation of the trigeminal brainstem complex by primary afferent fibers containing calcitonin gene‐related peptide , 1992, The Journal of comparative neurology.

[12]  W M Cowan,et al.  Topographic targeting errors in the retinocollicular projection and their elimination by selective ganglion cell death , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  D. O'Leary,et al.  Potential of visual cortex to develop an array of functional units unique to somatosensory cortex , 1991, Science.

[14]  E. Shooter,et al.  A monoclonal antibody modulates the interaction of nerve growth factor with PC12 cells. , 1984, The Journal of biological chemistry.

[15]  L. Sikich,et al.  Effect of a uniform partial denervation of the periphery on the peripheral and central vibrissal system in guinea pigs , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  M. Jacquin,et al.  Parvalbumin and calbindin immunocytochemistry reveal functionally distinct cell groups and vibrissa‐related patterns in the trigeminal brainstem complex of the adult rat , 1992, The Journal of comparative neurology.

[17]  V. Bocchini,et al.  The nerve growth factor: purification as a 30,000-molecular-weight protein. , 1969, Proceedings of the National Academy of Sciences of the United States of America.

[18]  H. Killackey,et al.  The development of vibrissae representation in subcortical trigeminal centers of the neonatal rat , 1979, The Journal of comparative neurology.

[19]  C. Ibáñez,et al.  Evolutionary studies of the nerve growth factor family reveal a novel member abundantly expressed in xenopus ovary , 1991, Neuron.

[20]  G M Innocenti,et al.  Growth and reshaping of axons in the establishment of visual callosal connections. , 1981, Science.

[21]  Richard E. Coggeshall,et al.  Calibration of methods for determining numbers of dorsal root ganglion cells , 1990, Journal of Neuroscience Methods.

[22]  H. Killackey,et al.  Differential organization of thalamic projection cells in the brain stem trigeminal complex of the rat , 1980, Brain Research.

[23]  W. Greenough,et al.  Dendritic pattern formation involves both oriented regression and oriented growth in the barrels of mouse somatosensory cortex. , 1988, Brain research.

[24]  J. Pearson,et al.  Dorsal root ganglion neurons are destroyed by exposure in utero to maternal antibody to nerve growth factor. , 1980, Science.

[25]  T. Woolsey,et al.  The structural organization of layer IV in the somatosensory region (S I) of mouse cerebral cortex , 1970 .

[26]  M. Barbacid,et al.  Expression of the trk proto-oncogene is restricted to the sensory cranial and spinal ganglia of neural crest origin in mouse development. , 1990, Genes & development.

[27]  H. van der Loos,et al.  Development of the barrels and barrel field in the somatosensory cortex of the mouse , 1977, The Journal of comparative neurology.

[28]  P. Distefano,et al.  trkB encodes a functional receptor for brain-derived neurotrophic factor and neurotrophin-3 but not nerve growth factor , 1991, Cell.

[29]  E. Johnson,et al.  Characterization of the binding properties and retrograde axonal transport of a monoclonal antibody directed against the rat nerve growth factor receptor , 1985, The Journal of cell biology.

[30]  H. Thoenen,et al.  Timing and site of nerve growth factor synthesis in developing skin in relation to innervation and expression of the receptor , 1987, Nature.

[31]  P. Ernfors,et al.  Cells Expressing mRNA for Neurotrophins and their Receptors During Embryonic Rat Development , 1992, The European journal of neuroscience.

[32]  E. Johnson,et al.  Experimental autoimmune model of nerve growth factor deprivation: effects on developing peripheral sympathetic and sensory neurons. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[33]  H. Killackey,et al.  Vibrissae representation in subcortical trigeminal centers of the neonatal rat , 1979, The Journal of comparative neurology.

[34]  R. Vongdokmai Effect of protein malnutrition on development of mouse cortical barrels , 1980, The Journal of comparative neurology.

[35]  P. Vos,et al.  Merkel cells in vitro: production of nerve growth factor and selective interactions with sensory neurons. , 1991, Developmental biology.

[36]  V. Hamburger,et al.  Neuronal death in the spinal ganglia of the chick embryo and its reduction by nerve growth factor , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  J. Arvidsson Somatotopic organization of vibrissae afferents in the trigeminal sensorynuclei of the rat studied by transganglionic transport of HRP , 1982, The Journal of comparative neurology.

[38]  N. Chiaia,et al.  Evidence for prenatal competition among the central arbors of trigeminal primary afferent neurons , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[39]  H. Killackey,et al.  Distinguishing topography and somatotopy in the thalamocortical projections of the developing rat. , 1985, Brain research.

[40]  Michael W. Miller,et al.  Birthdates of trigeminal ganglion cells contributing axons to the infraorbital nerve and specific vibrissal follicles in the rat , 1991, The Journal of comparative neurology.

[41]  M. Wong-Riley Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry , 1979, Brain Research.

[42]  R. Coggeshall,et al.  An empirical method for converting nucleolar counts to neuronal numbers , 1984, Journal of Neuroscience Methods.

[43]  I. W. Mclean,et al.  PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY , 1974, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[44]  T. Woolsey,et al.  Somatosensory Cortex: Structural Alterations following Early Injury to Sense Organs , 1973, Science.

[45]  M. Armstrong‐James,et al.  Spatiotemporal convergence and divergence in the rat S1 “Barrel” cortex , 1987, The Journal of comparative neurology.

[46]  S. Jhaveri,et al.  Trigeminal ganglion cell processes are spatially ordered prior to the differentiation of the vibrissa pad , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[47]  D. Kaplan,et al.  High-affinity NGF binding requires coexpression of the trk proto-oncogene and the low-affinity NGF receptor , 1991, Nature.

[48]  R S Erzurumlu,et al.  Thalamic axons confer a blueprint of the sensory periphery onto the developing rat somatosensory cortex. , 1990, Brain research. Developmental brain research.

[49]  M. Bothwell,et al.  Structure and developmental expression of the chicken NGF receptor. , 1990, Developmental biology.

[50]  M. Goedert,et al.  Requirement of nerve growth factor for development of substance P-containing sensory neurones , 1980, Nature.

[51]  R. Rhoades,et al.  Postnatal blockade of cortical activity by tetrodotoxin does not disrupt the formation of vibrissa-related patterns in the rat's somatosensory cortex. , 1992, Brain research. Developmental brain research.

[52]  Y. Barde,et al.  Identification and characterization of a novel member of the nerve growth factor/brain-derived neurotrophic factor family , 1990, Nature.

[53]  M. Constantine-Paton,et al.  Eye-specific segregation requires neural activity in three-eyed Rana pipiens , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[54]  H. Yip,et al.  Developing dorsal root ganglion neurons require trophic support from their central processes: evidence for a role of retrogradely transported nerve growth factor from the central nervous system to the periphery. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[55]  L. Belluscio,et al.  Neurotrophin-3: a neurotrophic factor related to NGF and BDNF. , 1990, Science.

[56]  P. Wall,et al.  Expansion of receptive fields in the mouse cortical barrelfield after administration of capsaicin to neonates or local application on the infraorbital nerve in adults , 1985, Brain Research.

[57]  Thomas A. Woolsey,et al.  Cytoarchitectonic correlates of the vibrissae in the medullary trigeminal complex of the mouse , 1984, Brain Research.

[58]  S. Turner Prenatal development. , 1988, The Lamp.

[59]  M. Jacquin,et al.  Structure and function of barrel 'precursor' cells in trigeminal nucleus principalis. , 1988, Brain research.

[60]  T. Woolsey Some anatomical bases of cortical somatotopic organization. , 1978, Brain, behavior and evolution.

[61]  M. Jacquin,et al.  Intra-axonal neurobiotin™ injection rapidly stains the long-range projections of identified trigeminal primary afferents in vivo: comparisons with HRP and PHA-L , 1992, Journal of Neuroscience Methods.

[62]  J. S. McCasland,et al.  2‐DG uptake patterns related to single vibrissae during exploratory behaviors in the hamster trigeminal system , 1993, The Journal of comparative neurology.

[63]  T. Hunter,et al.  The neurotrophic factors brain-derived neurotrophic factor and neurotrophin-3 are ligands for the trkB tyrosine kinase receptor , 1991, Cell.

[64]  Eugene M. Johnson,et al.  Destruction of sympathetic and sensory neurons in the developing rat by a monoclonal antibody against the nerve growth factor (NGF) receptor , 1989, Brain Research.

[65]  E. Fenton Tissue culture assay of nerve growth factor and of the specific antiserum. , 1970, Experimental cell research.

[66]  Thomas A. Woolsey,et al.  Some Anatomical Bases of Cortical Somatotopic Organization; pp. 325347 , 1978 .

[67]  R. Levi‐montalcini,et al.  The nerve growth factor 35 years later. , 1987, Science.

[68]  M. Jacquin,et al.  Reorganization of the peripheral projections of the trigeminal ganglion following neonatal transection of the infraorbital nerve. , 1987, Somatosensory research.

[69]  J. Milbrandt,et al.  Dorsal root ganglion neurons expressing trk are selectively sensitive to NGF deprivation in utero , 1992, Neuron.

[70]  M. Bothwell Tissue localization of nerve growth factor and nerve growth factor receptors. , 1991, Current topics in microbiology and immunology.

[71]  S. Thanos,et al.  Major role for neuronal death during brain development: refinement of topographical connections. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[72]  H. Yip,et al.  The effects of nerve growth factor and its antiserum on the postnatal development and survival after injury of sensory neurons in rat dorsal root ganglia , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[73]  E. Shooter,et al.  Molecular characteristics of nerve growth factor receptors on PC12 cells. , 1985, The Journal of biological chemistry.

[74]  R. Rhoades,et al.  Prenatal development of the receptive fields of individual trigeminal ganglion cells in the rat. , 1993, Journal of neurophysiology.

[75]  S. Hunt,et al.  Biochemical and anatomical effects of antibodies against nerve growth factor on developing rat sensory ganglia. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[76]  H. Killackey,et al.  The role of the principal sensory nucleus in central trigeminal pattern formation. , 1985, Brain research.

[77]  M F Jacquin,et al.  Infraorbital nerve blockade from birth does not disrupt central trigeminal pattern formation in the rat. , 1992, Brain research. Developmental brain research.

[78]  M. Jacquin,et al.  Functional consequences of neonatal infraorbital nerve section in rat trigeminal ganglion , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[79]  R. Rhoades,et al.  Effects of cortical and thalamic lesions upon primary afferent terminations, distributions of projection neurons, and the cytochrome oxidase pattern in the trigeminal brainstem complex , 1991, The Journal of comparative neurology.

[80]  M. Bothwell,et al.  Novel roles for neurotrophins are suggested by BDNF and NT-3 mRNA expression in developing neurons , 1992, Neuron.

[81]  M. Jacquin Structure‐function relationships in rat brainstem subnucleus interpolaris: V. Functional consequences of neonatal infraorbital nerve section , 1989, The Journal of comparative neurology.

[82]  C. Welt,et al.  Neurogenesis in the trigeminal ganglion of the albino rat: A quantitative autoradiographic study , 1981, The Journal of comparative neurology.

[83]  H. J. G. Gundersen,et al.  The new stereological tools: Disector, fractionator, nucleator and point sampled intercepts and their use in pathological research and diagnosis , 1988, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[84]  H. Nagura,et al.  Tissue localization of nerve growth factor receptors:trk A and low-affinity nerve growth factor receptor in neuroblastoma, pheochromocytoma, and retinoblastoma , 1996, Endocrine pathology.

[85]  M. Jacquin,et al.  Structure‐function relationships in the rat brainstem subnucleus interpolaris: II. Low and high threshold trigeminal primary afferents , 1988, The Journal of comparative neurology.

[86]  M. Barbacid,et al.  The trkB tyrosine protein kinase is a receptor for brain-derived neurotrophic factor and neurotrophin-3 , 1991, Cell.