Identification of extraretinal photoreceptors in the teleost Phoxinus phoxinus

Histology and Histopathology

Volumn 19, Issue 2, 2004, Pages 487-494

  Alvarez Viejo M ^a   Cernuda Cernuda, R ^a   Alvarez Lopez C ^a   García Fernández, José M ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

Hypothalamus; Non visual photoreceptors; Opsin; Pineal complex; Teleost

Indexed keywords

ALPHA TRANSDUCIN; MONOCLONAL ANTIBODY; POLYCLONAL ANTISERUM; RETINA S ANTIGEN; RHODOPSIN; TRANSDUCIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ANTIBODY LABELING; ARTICLE; BRAIN NERVE CELL; DEEP BRAIN PHOTORECEPTOR; EPITHALAMUS; GIANT CELL; HABENULA; HYPOTHALAMUS; HYPOTHALAMUS HYPOPHYSIS SYSTEM; IMMUNOCYTOCHEMISTRY; IMMUNOREACTIVITY; NERVE PROJECTION; NONHUMAN; PHOTOPERIODICITY; PHOTORECEPTOR; PHOTOSENSITIVITY; PHOTOTRANSDUCTION; PINEALOCYTE; PREOPTIC NUCLEUS; RETINA CONE; RETINA ROD; TELENCEPHALON; TELEOST;

ANIMALS; BRAIN; EPITHALAMUS; FISHES; HYPOTHALAMUS; IMMUNOHISTOCHEMISTRY; LIGHT; MODELS, BIOLOGICAL; NEURONS; OPSIN; PHOTORECEPTORS; RETINA; RODS (RETINA); TRANSDUCIN;

ANIMALIA; PHOXINUS; PHOXINUS PHOXINUS; TELEOST FISH; TELEOSTEI; VERTEBRATA;

EID: 1842454334     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (45)

1. Álvarez-Viejo M., Cernuda-Cernuda R., DeGrip W.J., Álvarez-López C. and García-Fernández J.M. (2003). Co-localization of mesotocin and opsin immunoreactivity in the hypothalamic preoptic nucleus of Xenopus laevis. Brain Res. 969, 36-43.
2. Bailhache T., Arazam A., Klungland H., Alestrom P., Breton B. and Jego P. (1994). Localization of salmon gonadotropin-releasing hormone mRNA and peptide in the brain of Atlantic salmon and rainbow trout. J. Comp. Neurol. 347, 444-454.
3. Blackshaw S. and Snyder S.H. (1997). Parapinopsin, a novel catfish opsin localized to the parapineal organ, defines a new gene family. J. Neurosci. 17, 8083-8092.
4. Cantera R., von Schantz M., Chader G.J., Ehinger B., Sanyal S. and van Veen T. (1990). Postnatal development of photoreceptor-specific proteins in mice with hereditary retinal degeneration. An immunocytochemical study. Exp. Biol. 48, 305-312.
5. Demski L.S. and Northcutt R.G. (1983). The terminal nerve: A new chemosensory system in vertebrates? Science 220, 435-437.
6. Drivenes O., Soviknes A.M., Ebbesson L.O.E., Fjose A., Seo H.C. and Helvik J.V. (2003). Isolation and characterization of two teleost melanopsin genes and their differential expression within the inner retina and brain. J. Comp. Neurol. 456, 84-93.
7. Ekström P. and Meissl H. (1997). The pineal organ of teleost fishes. Rev. Fish. Biol. Fisheries 7, 199-284.
8. Ebbesson S.O., Bazer G.T., Reynolds J.B. and Bailey R.P. (1988). Retinal projections in sockeye salmon smolts (Oncorhynchus nerka). Cell Tissue Res. 252, 215-218.
9. Ekström P., Borg B. and van Veen T. (1983). Ontogenetic development of the pineal organ, parapineal organ, and retina of the three-spined stickleback, Gasterosteus aculeatus L. (Teleostei). Development of photoreceptors. Cell Tissue Res. 233, 593-609.
10. Ekström P., Foster R.G., Korf H-W. and Schalken J.J. (1987). Antibodies against retinal photoreceptor-specific proteins reveal axonal projections from the photosensory pineal organ of teleosts. J. Comp. Neurol. 265, 25-33.
11. Foster R.G. and Follet B.K. (1985). The involvement of a rhodopsin-like photopigment in the photoperiodic response of the Japanese quail. J. Comp. Physiol. [A] 157, 519-528.
12. Foster R.G., Follet B.K. and Lythgoe J.N. (1985). Rhodopsin-like sensitivity of extra-retinal photoreceptors mediating the photoperiodic response in quail. Nature 313, 50-52.
13. Foster R.G., Timmers A.M., Schalken J.J. and DeGrip W.J. (1989). A comparasion of some photoreceptor characteristics in the pineal and retina: II. The Djungarian Hamster (Phodopus sungorus). J. Comp. Physiol. [A] 165, 565-572.
14. Foster R.G., García-Fernández J.M., Provencio I. and DeGrip W.J. (1993). Opsin localization and chromophore retinoids identified within the basal brain of the lizard Anolis carolinensis. J. Comp. Physiol. [A] 172, 33-45.
15. Foster R.G., Grace M.S., Provencio I., DeGrip W.J. and García-Fernández J.M. (1994). Identification of vertebrate deep brain photoreceptors. Neurosci. Biobehav. Rev. 18, 541-546.
16. Frisch K. von (1911). Beiträge zur Physiologie der Pigmentzenllen in der Fischhaut. Pflügers Arch. Gesamte. Physiol. Menschen Tiere 138, 319-387.
17. García-Fernńdez J.M. and Foster R.G. (1994). Immunocytochemical identification of photoreceptors proteins in hypothalamic cerebrospinal fluid-contacting neurons of the larval lamprey (Petromyzon marinus). Cell Tissue Res. 275, 319-326.
18. García-Fernández J.M., Jiménez A.J., Gonzá lez B., Pombal M.A. and Foster R.G. (1997). An immunocytochemical study of encephalic photoreceptors in three species of lamprey. Cell Tissue Res. 288, 267-278.
19. Hattar S., Liao H.W., Takao M., Berson D.M. and Yau K.W. (2002). Melanopsin-containing retinal ganglion cells: Architecture, projections, and intrinsic photosensitivity. Science 295, 1065-1070.
20. Hicks D. and Molday R.S. (1986). Differential immunogold-dextran labelling of bovine and frog rod and cone cells using monoclonal antibodies against bovine rhodopsin. Exp. Eye Res. 42, 55-71.
21. Korf H.W., Oksche A., Ekström P., Gery I., Zigler J.J. and Klein D.C. (1986). Pinealocyte projections into the mammalian brain revealed by S-antigen antiserum. Science 231, 735-737.
22. Korf H.W., Sato T. and Oksche A. (1990). Complex relationships between the pineal organ and the medial habenular nucleus-pretectal region of the mouse as revealed by S-antigen inmmunocytochemistry. Cell Tissue Res. 262, 493-500.
23. Mano H., Kojima D. and Fukada Y. (1999). Exo-rhodopsin: A novel rhodopsin expressed in the zebrafish pineal gland. Brain Res. Mol. Brain Res. 73, 110-118.
24. Max M., McKinnon P.J., Seidenman K.J., Barrett R.K., Applebury M.L., Takahashi J.S. and Margolskee R.F. (1995). Pineal opsin: a nonvisual opsin expressed in chick pineal. Science 267, 1502-1506.
25. Okano T., Yoshizawa T. and Fukada Y. (1994). Pinopsin is a chicken pineal photoreceptive molecule. Nature 372, 94-97.
26. Okano K., Okano T.,Yoshikawa T., Masuda A., Fukada Y. and Oishi T. (2000) Diversity of opsin immunoreactivities in the extraretinal tissues of four anuran amphibians. J. Exp. Zool. 286, 136-1 42.
27. Peter R.E. and Fryer J.N. (1983). Endocrine functions of the hypothalamus of actinopterygians. In: Fish neurobiology. vol 2, Higher brain areas and functions. Davis R.E. and Northcutt R.G. (eds.). The University of Michigan Press. Ann Arbor. pp 165-201.
28. Philp A.R., García- Fernández J.M., Soni B.G., Lucas J.R. and Bellingham J., Foster R.G. (2000a). Vertebrate Ancient (VA) opsin and extraretinal photoreception in the Atlantic salmon (Salmo salar). Exp. Biol. 203, 1925-1936.
29. Philp A.R., Bellingham J., García-Fernández J.M. and Foster R.G. (2000b). A novel rod-like opsin isolated from extra-retinal photoreceptors of teleost fish. FEBS Lett 468, 181-188.
30. Provencio I., Jiang G., DeGrip W.J., Hayes W. and Rollag M.D. (1998). Melanopsin: An opsin in melanophores, brain, and eye. Proc. Natl. Acad. Sci. USA 95, 340-345.
31. Provencio I., Rollag M.D. and Castrucci A.M. (2002). Photoreceptive net in the mammalian retina. This mesh of cells may explain how some blind mice can still tell day from night. Nature 415, 493.
32. Rudeberg C. (1969). Structure of the parapineal organ of the adult rainbow trout, Salmo gairdneri Richardson. Z. Zellforsch Mikrosk. Anat. 93, 282-304.
33. Saldanha G.J., Leak R.K. and Silver R. (1994). Detection and transduction of daylength in birds. Psychoneuroendocrinology 19, 641-656. Review.
34. Saldanha C.J., Silverman A.J. and Silver R. (2001). Direct innervation of Gn-RH neurons by encephalic photoreceptors in birds. J. Biol. Rhythms 16, 39-49.
35. Schalken J.J. and DeGrip W.J. (1986). Enzyme-linked immunosorbent assay for quantitative determination of the visual pigment rhodopsin in total-eye extracts. Exp. Eye Res. 43, 431-439.
36. Scharrer E. (1928) Die Lichtempfindlichkeit blinder Elritzen I. Untersuchungen über Zwischenhirn der Fische. Z. Vergl. Physiol. 7, 1-38.
37. Scharrer E. (1964). Photoneuroendocrine systems: General concepts. Ann. N.Y. Acad. Sci. 117, 13-22.
38. Silver R., Witkovsky P., Alones V., Barnstable C.J. and Lehman M.N. (1988). Coexpression of opsin-and VIP-like-immunoreactivity in CFS-contacting neurons of the avian brain. Cell Tissue Res. 253, 189-198.
39. Soni B.G. and Foster R.G. (1997) A novel and ancient vertebrate opsin. FEBS. Letters 406, 279-283.
40. Vigh B., Manzano M.J., Zádori A., Frank C.L., Lukáts A., Röhlich P., Szél A. and Dávid C. (2002). Nonvisual photoreceptors of the deep brain, pineal organs and retina. Histol. Histopathol. 17, 555-590.
41. Vollrath L. (1981). The pineal organ. In: Handbuch der mikroskopischen anatomie des menschen. VI/7. Oksche A. and Vollrath L. (eds.). Springer. Berlin-Heidelberg-New York. Pp 1-665.
42. Yanez J. and Anadáon R. (1996). Afferent and efferent connections of the habenula in the rainbow trout (Oncorhynchus mykiss): an indocarbocyanine dye (Dil) study. J. Comp. Neurol. 372, 529-543.
43. Yanez J., Meissl H. and Anadón R. (1996). Central projections of the parapineal organ of the adult rainbow trout (Oncorhynchus mykiss). Cell Tissue Res. 285, 69-74.
44. Yoshikawa T., Okano T., Oishi T. and Fukada Y. (1998). A deep brain photoreceptive molecule in the toad hypothalamus. FEBS Lett- 424, 69-72.
45. Yoshikawa T., Yashiro Y., Oishi T., Kokame K. and Fukada Y. (1994). Immunoreactivities rhodopsin and rod/cone transducin antisera in the retina, pineal complex and deep brain of the bullfrog, Rana catesbeiana. Zoolog. Sci. 11, 675-80.