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An ultrastructural study of glomeruli associated with vomeronasal organs transplanted into the rat CNS

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Abstract

Rat neonate vomeronasal organs were transplanted into the parietal cortex of littermates to examine their survival and the behavior of axon growth into the surrounding host brain parenchyma. After survival times of 10–100 days the brains were processed for ultrastructural examination. The transplanted vomeronasal organs (VNO) formed several vesicles lined with a sensory epithelium. From these sensory epithelia, VNO neurons leave the epithelium and enter the host brain. Transplant neurons grew axons that fasciculated into bundles surrounded by sheath cell processes and formed one or more fiber plexuses containing distinct globose or spherical-shaped glomeralar-like structures. The glomeruli consisted of nerve terminals between which existed asymmetric synaptic contacts. Rarely did we observe clear reciprocal synapses. The glomeruli also contained terminals that showed signs of degeneration, such as increased density of the terminals, clumping of mitochondria and multivesicular bodies. The glomeruli were not partitioned or subdivided by glial septa; however, glial profiles were interspersed among the sensory terminals. Transplant glomeruli also lacked periglomerular cells and had no definitive glial envelope. These results suggest that glomerular formation is not dependent on dendrite contribution of second order neurons or glial support, but rather on a complementary population of receptor neurons.

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References

  • Brunjes PC, Frazier LL (1986) Maturation and plasticity in the olfactory system of vertebrates. Brain Res Rev 11:1–45

    Google Scholar 

  • Chuah MI, Au C (1991) Olfactory Schwann cells are derived form precursor cells in the olfactory epithelium. J Neurosci Res 29:172–180

    Google Scholar 

  • Doucette R (1989) Development of the nerve fiber layer in the olfactory bulb of mouse embryo. J Comp Neurol 285:514–527

    Google Scholar 

  • Graziadei PPC (1990) Olfactory development. In: Coleman JR (ed) Development of sensory systems in mammals. Wiley, New York, pp 519–566

    Google Scholar 

  • Graziadei PPC, Monti Graziadei GA (1986a) Neuronal changes in the forebrain of mice following penetration of regenerating olfactory axons. J Comp Neurol 247:344–356

    Google Scholar 

  • Graziadei PPC, Monti Graziadei GA (1986b) Principles of organization of the vertebrate olfactory glomerulus: an hypothesis. Neuroscience 19:1025–1035

    Google Scholar 

  • Graziadei PPC, Samanen DW (1980) Ectopic glomerular structures in the olfactory bulb of neonatal and adult mice. Brain Res 187:467–472

    Google Scholar 

  • Graziadei PPC, Levine RR, Monti Graziadei GA (1978) Regeneration of olfactory axons and synapse formation in forebrain after bulbectomy in neonatal mice. Proc Natl Acad Sci USA 75:5230–5234

    Google Scholar 

  • Graziadei PPC, Levine RR, Monti Graziadei GA (1979) Plasticity of connections of the olfactory sensory neuron: regeneration into the forebrain following bulbectomy in neonatal mouse. Neuroscience 4:713–727

    Google Scholar 

  • Koo H, Graziadei PPC (1995a) Cell migration from the transplanted olfactory placode in Xenopus. Anat Embryol 191:171–187

    Google Scholar 

  • Koo H, Graziadei PPC (1995b) Eye primordium transplantation in Xenopus embryos. Anat Embryol 191:155–170

    Google Scholar 

  • Magrassi L, Graziadei PPC (1985) Interaction of the transplanted olfactory organ with the optic stalk and the diencephalon in Xenopus laevis embryos. Neuroscience 15:903–921

    Google Scholar 

  • Magrassi L, Graziadei PPC (1994) Developmental potential of cells dissociated from the mature and developing olfactory organ and transplanted into the fetal brain. Soc Neurosci Abstract, November 13–18, Miami Beach, Fla. No. 280.18

  • Monti Graziadei AG (1992) Cell migration from the olfactory neuroepithelium of neonatal and adult rodents. Brain Res Dev Brain Res 70:65–74

    Google Scholar 

  • Monti Graziadei GA, Graziadei PPC (1984) The olfactory organ. Neural transplantation. In: Sladek JR Jr, Gash DM (eds) Neural transplants, chap 6. Plenum Press, New York, pp 167–186

    Google Scholar 

  • Monti Graziadei GA, Graziadei PPC (1989) Experimental studies on the olfactory marker protein. V. Olfactory marker protein in the olfactory neurons transplanted within the olfactory bulb. Brain Res 484:157–167

    Google Scholar 

  • Monti Graziadei GA, Graziadei PPC (1992) Sensory reinnervation after partial removal of the olfactory bulb. J Comp Neurol 316:32–44

    Google Scholar 

  • Morrison EE, Graziadei PPC (1983) Transplants of olfactory mucosa in the rat brain. I. A light microscopic study of transplant organization. Brain Res 279:241–245

    Google Scholar 

  • Morrison EE, Graziadei PPC (1995) Transplantation of postnatal vomeronasal organ in the CNS of newborn rats. Anat Embryol 191:319–327

    Google Scholar 

  • Schwanzel-Fukuda M, Abraham MS, Crossin KL, Edelman GM, Pfaff DW (1992) Immunocytochemical demonstration of neural cell adhesion molecule (N-CAM) along the migration route of luteinizing-hormone-releasing-hormone (LHRH) neurons in mice. J Comp Neurol 321:1–8

    Google Scholar 

  • Schwanzel-Fukuda M, Reinhard S, Abraham S, Crossin KL, Edelman GM, Pfaff DW (1994) Antibody to neural cell adhesion molecule can disrupt the migration of luteinizing hormone-releasing hormone neurons into the mouse brain. J Comp Neurol 342:174–185

    Google Scholar 

  • Stanley RS (1979) A histological study of the prenatal development of the peripheral olfactory system in mouse (Mus musculus). Thesis, Florida State University, Tallahassee, Florida, USA

    Google Scholar 

  • Valverde F, Santacana M, Heredia M (1992) Formation of an olfactory glomerulus: morphological aspects of development and organization. Neuroscience 49:255–275

    Google Scholar 

  • Valverde F, Heredia M, Santacana M (1993) Characterization of neuronal cell varieties migrating from the olfactory epithelium during prenatal development in the rat — immunocytochemical study using antibodies against olfactory marker protein (OMP) and luteinizing-hormone-releasing-hormone (LHRH). Brain Res Dev Brain Res 71:209–220

    Google Scholar 

  • Wray S, Nieburgs A, Elkabes S (1989) Spatiotemporal cell expression of luteinizing-hormone-releasing-hormone in the prenatal mouse: evidence for an embryonic origin in the olfactory placode. Brain Res Dev Brain Res 46:309–318

    Google Scholar 

  • Wray S, Grant P, Gainer H (1990) Evidence that cells expressing luteinizing-hormone-releasing-hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode. Proc Natl Acad Sci USA 86:8132–8136

    Google Scholar 

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Morrison, E.E., Graziadei, P.P.C. An ultrastructural study of glomeruli associated with vomeronasal organs transplanted into the rat CNS. Anat Embryol 193, 331–339 (1996). https://doi.org/10.1007/BF00186690

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