Skip to main content
Log in

Basal cells in the mouse olfactory epithelium after axotomy: immunohistochemical and electron-microscopic studies

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Summary

The olfactory epithelium of mice after axotomy was investigated to clarify the stem cells of olfactory cells by double immunostaining using antikeratin (MA903) and anti-bromodeoxyuridine (BrdU) antibodies and by conventional electron microscopy. When a single dose of BrdU was given to mice 9 days after axotomy, immunostaining for BrdU was found in the globose basal cells which were negative for MA903, but not in the basal cells proper which were positive for MA903. The BrdU-immunoreactive cells increased 3-to 6-fold over the number of these cells in the controls, indicating active cell proliferation. At other postoperative days (4 and 14 days), fewer BrdU-immunoreactive cells were found. Furthermore, three pulses of BrdU resulted in numerous BrdU-immunolabelings in the globose basal cells and a few in the basal cells proper. There was no detectable difference in the number of labeled basal cells proper in operated and unoperated mice. In the electron micrographs 9 days after axotomy, the basal cells proper, flat-shaped in unoperated mice, appeared cylindrical or pyramidal in shape and the globose basal cells often lay between the basal cells proper. In unoperated controls, the globose basal cells were located above the flat-shaped basal cells proper. The results suggest that the stem cells of the olfactory cells are globose basal cells and not basal cells proper, and that the shape of basal cells proper changes in relation to the active proliferation of stem cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Andres KH (1969) Der olfaktorische Saum der Katze. Z Zellforsch 96:250–274

    Google Scholar 

  • Calof AL, Chikaraishi DM (1989) Analysis of neurogenesis in mammalian neuroepithelium: proliferation and differentiation of an olfactory neuron precursor in vitro. Neuron 3:115–127

    Google Scholar 

  • Carr VM, Farbman AI, Lidow MS, Colletti LM, Hempstead JL, Morgan JI (1989) Developmental expression of reactivity to monoclonal antibodies generated against olfactory epithelia. J Neuroscience 9:1179–1198

    Google Scholar 

  • Constanzo RM, Graziadei PPC (1987) Development and plasticity of the olfactory system. In: Finger TE, Silver WL (eds) Neurobiology of taste and smell. Wiley, New York Chichester Brisbane, pp 233–250

    Google Scholar 

  • Farbman AI (1990) Olfactory neurogenesis: genetic or environmental controls? Trends Neurosci 13:362–365

    Google Scholar 

  • Gratzner HG (1982) Monoclonal antibody to 5-bromo-and 5-iododeoxyuridine: a new reagent for detection of DNA replication. Science 218:474–475

    Google Scholar 

  • Graziadei PPC, Metcalf JF (1971) Autoradiogrpahic and ultrastructural observations in the frog's olfactory mucosa. Z Zellforsch 116:305–318

    Google Scholar 

  • Graziadei PPC, Monti-Graziadei GA (1979) Neurogenesis and neuron regeneration in the olfactory system of mammals. 1. Morpholgoical aspects of differentiation and structural organization of the olfactory sensory neurons. J Neurocytol 8:1–18

    Google Scholar 

  • Graziadei PPC, Karlan MS, Monti-Graziadei GA, Bernstein JJ (1980) Neurogenesis of sensory neurons in the primate olfactory system after section of the fila olfactoria. Brain Res 186:289–300

    Google Scholar 

  • Harms G, Goor H van, Koudstaal J, Ley L de (1986) Immunohistochemical demonstration of DNA-incorporated 5-bromodeoxyuridine in frozen and plastic embedded sections. Histochemistry 85:139–143

    Google Scholar 

  • Key B, Akeson RA (1990) Immunochemical markers for the frog olfactory neuroepithelium. Dev Brain Res 57:103–117

    Google Scholar 

  • Mackay-Sim A, Patel U (1984) Regional differences in cell density and cell genesis in the olfactory epithelium of the salamander, Ambystoma tigrium. Exp Brain Res 57:99–106

    Google Scholar 

  • Miragall F, Monti-Graziadei GA (1982) Experimental studies on the olfactory marker protein. II Appearance of the olfactory marker protein during differentiation of the olfactory sensory neurons of mouse: an immunohistochemical and autoradiographic study. Brain Res 239:245–250

    Google Scholar 

  • Miragall F, Kadmon G, Husmann M, Schachner M (1988) Expression of cell adhesion molecules in the olfactory system of the adult mouse: presence of the embryonic form of N-CAM. Dev Biol 129:516–531

    Google Scholar 

  • Monti-Graziadei GA, Graziadei PPC (1979) Neurogenesis and neuron regeneration in the olfactory system of mammals. II Degeneration and regeneration of olfactory sensory neurons after axotomy. J Neurocytol 8:197–213

    Google Scholar 

  • Morrison EE, Constanzo RM (1989) Scanning electron microscopic study of degeneration and regeneration in the olfactory epithelium after axotomy. J Neurocytol 18:393–405

    Google Scholar 

  • Nagahara Y (1940) Experimentalle Studien über die histologischen Veränderungen des Geruchsorgans nach der Olfaktorius-durchschneidung —Beiträge zur Kenntnis des feineres Baus des Geruchsorgans. Jpn J Med Sci V Pathol 5:165–199

    Google Scholar 

  • Onoa N (1988) Monoclonal antibody immunohistochemistry of degenerative and renewal patterns in rabbit olfactory receptor neurons following unilateral olfactory bulbectomy. Neuroscience 26:1013–1022

    Google Scholar 

  • Simmons PA, Rafols JA, Getchell TV (1981) Ultrastructural changes in olfactory receptor neurons following olfactory nerve section. J Comp Neurol 197:237–257

    Google Scholar 

  • Suzuki Y, Takeda M (1991) Keratins in the developing olfactory epithelia. Dev Brain Res 59:171–178

    Google Scholar 

  • Vollrath M, Altmannsberger M, Weber K, Osborn M (1985) An ultrastructural and immunohistological study of the rat olfactory epithelium: unique properties of olfactory cells. Differentiation 29:243–253

    Google Scholar 

  • Wang RT, Halpern M (1982a) Neurogenesis in the vomeronasal epithelium of adult garter snakes. 1. Degeneration of bipolar neurons and proliferation of undifferentiated cells following experimental vomeronasal axotomy. Brain Res 237:23–39

    Google Scholar 

  • Wang RT, Halpern M (1982b) Neurogenesis in the vomeronasal epithelium of adult garter snakes. 2. Reconstitution of the bipolar neuron layer following experimental vomeronasal axotomy. Brain Res 237:47–59

    Google Scholar 

  • Yamagishi M, Hasegawa S, Takahashi S, Nakano Y, Iwanaga T (1989a) Immunohistochemical analysis of the olfactory mucosa by use of antibodies to brain proteins and cytokeratin. Ann Otol Rhinol Laryngol 98:384–388

    Google Scholar 

  • Yamagishi M, Nakamura H, Takahashi S, Nakano Y, Iwanaga T (1989b) Olfactory receptor cells: immunocytochemistry for nervous system-specific proteins and re-evaluation of their precursor cells. Arch Histol Cytol 52 [Suppl]:375–381

    Google Scholar 

  • Yamamoto M (1976) An electron microscopic study of the olfactory mucosa in the bat and rabbit. Arch Histol Jpn 38:359–412

    Google Scholar 

  • Yamamoto M, Uchida K, Ito T (1976) Regeneration of olfactory bipolar neurons in the normal olfactory epithelium of the adult bat. Okajimas Folia Anat Jpn 53:291–304

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Suzuki, Y., Takeda, M. Basal cells in the mouse olfactory epithelium after axotomy: immunohistochemical and electron-microscopic studies. Cell Tissue Res 266, 239–245 (1991). https://doi.org/10.1007/BF00318179

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00318179

Key words

Navigation