Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1986 Aug;83(15):5736–5740. doi: 10.1073/pnas.83.15.5736

Substance P-containing ganglion cells become progressively less detectable during retinotectal development in the frog Rana pipiens.

R O Kuljis, H J Karten
PMCID: PMC386364  PMID: 2426705

Abstract

Substance P-like immunoreactivity (SPLI) was immunohistochemically analyzed in the retinae and optic tecta of Rana pipiens embryos and tadpoles between stages 25 of Shumway (S25) and XXV of Taylor and Kollros (TKXXV). A population of retinal ganglion cell (RGC) somata display SPLI. The number of labeled cell bodies increases in proportion and staining intensity between S25 and TKX and progressively decreases toward the end of metamorphosis. At TKXXV, only occasional cells in the periphery of the retina displaying SPLI can be observed in the RGC layer, heralding the adult condition, in which SPLI can only be seen rarely in occasional RGCs. An increasing proportion of optic nerve axons display SPLI from S25 through TKXVI, decreasing progressively thereafter toward the end of the larval period. Concurrently, SPLI appears for the first time in the superficial tectal neuropil between TKIII and TKV, with progressively increasing staining intensity and in a discrete lamina previously shown to contain retinofugal terminals in the adult. These observations corroborate inferences from previous studies indicating the existence of populations of peptidergic RGCs that terminate within precisely restricted synaptic loci in the tectum and presumably perform different functional operations in the adult. Previous observations, however, necessitated various experimental manipulations involving injuries to the visual system in order to demonstrate neuroactive peptide-like immunoreactivity in RGCs, thus allowing the possibility of posttraumatic expression of anomalous peptide phenotypes that may not reflect normal features of RGCs. The present study eliminates this variable and provides further evidence of the existence of peptidergic RGCs.

Full text

PDF
5736

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. COONS A. H. Fluorescent antibody methods. Gen Cytochem Methods. 1958;1:399–422. [PubMed] [Google Scholar]
  2. Currie J., Cowan W. M. The development of the retino-tectal projection in Rana pipiens. Dev Biol. 1975 Sep;46(1):103–119. doi: 10.1016/0012-1606(75)90090-1. [DOI] [PubMed] [Google Scholar]
  3. Hollyfield J. G. Differential addition of cells to the retina in Rana pipiens tadpoles. Dev Biol. 1968 Aug;18(2):163–179. doi: 10.1016/0012-1606(68)90041-9. [DOI] [PubMed] [Google Scholar]
  4. Kuljis R. O., Karten H. J. Laminar organization of peptide-like immunoreactivity in the anuran optic tectum. J Comp Neurol. 1982 Dec 1;212(2):188–201. doi: 10.1002/cne.902120208. [DOI] [PubMed] [Google Scholar]
  5. Kuljis R. O., Karten H. J. Modifications in the laminar organization of peptide-like immunoreactivity in the anuran optic tectum following retinal deafferentation. J Comp Neurol. 1983 Jul 1;217(3):239–251. doi: 10.1002/cne.902170302. [DOI] [PubMed] [Google Scholar]
  6. Kuljis R. O., Karten H. J. Regeneration of peptide-containing retinofugal axons into the optic tectum with reappearance of a substance P-containing lamina. J Comp Neurol. 1985 Oct 1;240(1):1–15. doi: 10.1002/cne.902400102. [DOI] [PubMed] [Google Scholar]
  7. Kuljis R. O., Krause J. E., Karten H. J. Peptide-like immunoreactivity in anuran optic nerve fibers. J Comp Neurol. 1984 Jun 20;226(2):222–237. doi: 10.1002/cne.902260206. [DOI] [PubMed] [Google Scholar]
  8. MATURANA H. R., LETTVIN J. Y., MCCULLOCH W. S., PITTS W. H. Anatomy and physiology of vision in the frog (Rana pipiens). J Gen Physiol. 1960 Jul;43(6):129–175. doi: 10.1085/jgp.43.6.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Maturana H. R., Lettvin J. Y., McCulloch W. S., Pitts W. H. Evidence That Cut Optic Nerve Fibers in a Frog Regenerate to Their Proper Places in the Tectum. Science. 1959 Dec 18;130(3390):1709–1710. doi: 10.1126/science.130.3390.1709. [DOI] [PubMed] [Google Scholar]
  10. McLean I. W., Nakane P. K. Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoelectron microscopy. J Histochem Cytochem. 1974 Dec;22(12):1077–1083. doi: 10.1177/22.12.1077. [DOI] [PubMed] [Google Scholar]
  11. Vandesande F. A critical review of immunocytochemical methods for light microscopy. J Neurosci Methods. 1979 Mar;1(1):3–23. doi: 10.1016/0165-0270(79)90003-7. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES