Abstract
Fish grow throughout life1 and new neurones are added to the retina as the eyes increase in size2–6. As the retina expands, the density of cells decreases: ganglion cells, cones and cells in the inner nuclear layer are spaced further apart in retinas from larger (older) fish2–5,7–9. In contrast, the density of rods increases during larval development and is then maintained approximately constant as the adult eye grows2–5. Previous developmental studies, in which 3H-thymidine was used to identify proliferating cells, revealed a germinal zone at the margin of the retina. The germinal cells divide to produce new retinal neurones which are added annularly at the perimeter of the growing retina5,6,10. A similar circumferential pattern of growth has been demonstrated in larval amphibians11–15. These studies concluded that the retinal margin is the only site of neurogenesis in post-embryonic retinas. In contrast, our observations suggest that new rods originate from mitotic divisions of precursor cells which are interspersed among the nuclei of mature rods within the retina. The selective addition of rods throughout the retina could explain how the proportion of rods relative to other neurones increases as the retinas of fish grow2–4,7. Preliminary reports of these experiments have appeared elsewhere16,17.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Brown, M. E. The Physiology of Fishes Vol. 1 (Academic, New York, 1957).
Müller, H. Zool. Jb. 63, 275–324 (1952).
Lyall, A. H. Q. Jl micros. Sci. 98, 101–110 (1957).
Wagner, H.-J. Z. Morph. Okol. Tiere. 79, 113–131 (1974).
Johns, P. R. J. comp. Neurol. 176, 343–358 (1977).
Meyer, R. L. Expl Neurol. 59, 99–111 (1978).
Johns, P. R. & Easter, S. S. J. comp. Neurol. 176, 331–342 (1977).
Ali, M. A. Growth 27, 57–76 (1963); 28, 83–89 (1964).
Kock, J.-H. & Reuter, T. J. comp. Neurol. 179, 533 (1978).
Scholes, J. H. in Neural Principles in Vision (eds Zettler, F. & Weiler, R.) 63–93 (Springer, New York, 1976).
Gaze, R. M. & Watson, W. E. in Growth of the Nervous System (eds Wolstenholme, G. E. W. & O'Connor, M.) 53–67 (Churchill, London, 1968).
Hollyfield, J. G. Devl Biol. 18, 163–179 (1968).
Straznicky, K. & Gaze, R. M. J. Embryol. exp. Morph. 26, 67–79 (1971).
Jacobson, M. Brain Res. 103, 541–545 (1976).
Beach, D. H. & Jacobson, M. J. comp. Neurol. 183, 603–614 (1979).
Johns, P. R. Neurosci. Abstr. 6, 639 (1980).
Fernald, R. D. & Johns, P. R. Neurosci. Abstr. 6, 208 (1980).
Cleaver, J. E. Thymidine Metabolism and Cell Kinetics (North-Holland, Amsterdam, 1967).
Rogers, A. W. Techniques in Autoradiography (Elsevier, Amsterdam, 1967).
Wünder, W. Z. vergl. Physiol. 3, 1–61 (1925).
Walls, G. L. The Vertebrate Eye and Its Adaptive Radiation (Hafner, New York, 1967).
Fraley, N. & Fernald, R. D. Z.f. Tierpych. (submitted).
Blaxter, J. H. S. in Vision in Fishes: New Approaches in Research, 427–444 (Plenum, New York, 1975).
Blaxter, J. H. S. & Jones, M. P. J. mar. Biol. Ass. U.K. 47, 677–679 (1967).
Blaxter, J. H. S. & Staines, M. J. mar. Biol. Ass. U.K. 50, 449–460 (1970).
Bernard, H. M. Q. Jl micros. Sci. 43, 23–47 (1900).
Lyall, A. H. Q. Jl micros. Sci. 98, 189–201 (1957).
Tamura, T. Bull. Jap. Soc. Sci. Fish. 22, 536–557 (1957).
Easter, S. S., Johns, P. R. & Baumann, L. Vision Res. 17, 469–477 (1977).
Sandy & Blaxter, J. H. S. J. mar. biol. Ass. U.K. 60, 59–71 (1980).
Johns, P. R. Invest. Ophthal. vis. Sci. Suppl. 20, 150 (1981).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Johns, P., Fernald, R. Genesis of rods in teleost fish retina. Nature 293, 141–142 (1981). https://doi.org/10.1038/293141a0
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/293141a0
This article is cited by
-
Bioengineering strategies for restoring vision
Nature Biomedical Engineering (2022)
-
β-SNAP activity in the outer segment growth period is critical for preventing BNip1-dependent apoptosis in zebrafish photoreceptors
Scientific Reports (2020)
-
Injury-induced purinergic signalling molecules upregulate pluripotency gene expression and mitotic activity of progenitor cells in the zebrafish retina
Purinergic Signalling (2017)
-
Presynaptic partner selection during retinal circuit reassembly varies with timing of neuronal regeneration in vivo
Nature Communications (2016)
-
Müller glial cell reprogramming and retina regeneration
Nature Reviews Neuroscience (2014)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.