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Coexpression of MT1 and ROR α1 melatonin receptors in the Syrian hamster Harderian gland.

Authors :
Tomás-Zapico, Cristina
Boga, José Antonio
Caballero, Beatriz
Vega-Naredo, Ignacio
Sierra, Verónica
Álvarez-García, Óscar
Tolivia, Delio
Rodríguez-Colunga, María Josefa
Coto-Montes, Ana
Source :
Journal of Pineal Research; Aug2005, Vol. 39 Issue 1, p21-26, 6p, 2 Diagrams, 1 Chart
Publication Year :
2005

Abstract

Melatonin acts through several specific receptors, including membrane receptors (MT<subscript>1</subscript> and MT<subscript>2</subscript>) and members of the RZR/ROR nuclear receptors family, which have been identified in a large variety of mammalian and nonmammalian cells types. Both membrane and nuclear melatonin receptors have been partially characterized in Harderian gland of the Syrian hamster. Nevertheless, the identities of these receptors were unknown until this study, where the coexistence of MT<subscript>1</subscript> and ROR α<subscript>1</subscript> in this gland was determined by nested RT-PCR followed by amplicon sequencing and Western-blot. Furthermore, the cellular localization of both receptors was determined by immunohistochemistry. Thus, MT<subscript>1</subscript> receptor was localized exclusively at the basal side of the cell acini, supporting the hypothesis that this receptor is activated by the pineal-synthesized melatonin. On the contrary, although a ROR α<subscript>1</subscript>-immunoreactivity was observed in nuclei of epithelial cells of both sexes, an extranuclear specific staining, which was more frequently among those cells of males, was also seen. The implication of this possible nuclear exclusion of ROR α<subscript>1</subscript> on the role of this indoleamine against oxidative stress is discussed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07423098
Volume :
39
Issue :
1
Database :
Complementary Index
Journal :
Journal of Pineal Research
Publication Type :
Academic Journal
Accession number :
17400697
Full Text :
https://doi.org/10.1111/j.1600-079X.2005.00210.x