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Circadian expression of tryptophan hydroxylase mRNA in the chicken retina

Producción científica: Article › revisión exhaustiva

53 Citas (Scopus)

Resumen

Many aspects of retinal physiology are controlled by a circadian clock located within the eye. This clock controls the rhythmic synthesis of melatonin, which results in elevated levels during the night and low levels during the day. The rate-limiting enzyme in melatonin biosynthesis in retina appears to be tryptophan hydroxylase (TPH)[G.M. Cahill and J.C. Besharse, Circadian regulation of melatonin in the retina of Xenopus laevis: Limitation by serotonin availability, J. Neurochem. 54 (1990) 716-719]. In this report, we found that TPH mRNA is strongly expressed in the photoreceptor layer and the vitread portion of the inner nuclear layer; the message is also expressed, but to a lesser extent, in the ganglion cell layer. The abundance of retinal TPH mRNA exhibits a circadian rhythm which persists in constant light or constant darkness. The phase of the rhythm can be reversed by reversing the light:dark cycle. In parallel experiments we found a similar pattern of expression in the chicken pineal gland. However, whereas a pulse of light at midnight suppressed retinal TPH mRNA by 25%, it did not alter pineal TPH mRNA, suggesting that there are tissue-specific differences in photic regulation of TPH mRNA. In retinas treated with kainic acid to destroy serotonin-containing amacrine and bipolar cells, a high amplitude rhythm of TPH mRNA was observed indicating that melatonin-synthesizing photoreceptors are the primary source of the rhythmic message. These observations provide the first evidence that chick retinal TPH mRNA is under control of a circadian clock. Copyright (C) 1998 Elsevier Science B.V.

Idioma originalEnglish
Páginas (desde-hasta)243-250
Número de páginas8
PublicaciónMolecular Brain Research
Volumen61
N.º1-2
DOI
EstadoPublished - oct 30 1998

Nota bibliográfica

Funding Information:
The authors wish to thank Leo Goe and Rashidul Haque (Emory University School of Medicine) for excellent technical assistance. This research was supported in part by NIH grant EY04864.

Financiación

The authors wish to thank Leo Goe and Rashidul Haque (Emory University School of Medicine) for excellent technical assistance. This research was supported in part by NIH grant EY04864.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Eye Institute (NEI)R01EY004864

    ASJC Scopus subject areas

    • Molecular Biology
    • Cellular and Molecular Neuroscience

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