z-logo
Premium
The Light‐Induced FOS Response in Melanopsin Expressing HEK ‐293 Cells is Correlated with Melanopsin Quantity and Dependent on Light Duration and Irradiance
Author(s) -
Georg Birgitte,
Rask Lene,
Hannibal Jens,
Fahrenkrug Jan
Publication year - 2014
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/php.12298
Subject(s) - melanopsin , messenger rna , biology , hek 293 cells , microbiology and biotechnology , blue light , chemistry , cell culture , neuroscience , retina , biochemistry , photopigment , physics , optics , genetics , gene
Abstract We established a cell line (HEK‐ hM el) expressing melanopsin in a tetracycline dependent manner to elucidate new aspects of melanopsin's light response. Different light stimuli were evaluated using FOS expression as response parameter. Immunoblotting was used to evaluate expression of melanopsin and FOS and qPCR to quantify FOS mRNA responses. The magnitude of the FOS response was found to correlate with the amount of melanopsin expressed by the cells, and a transient FOS mRNA induction followed by FOS protein still elevated after 24 h of illumination was revealed. Exposing the cells to darkness after light resulted in reduction of the response compared to exposure to light solely showing dependency on continuous light. Increasing irradiances of blue light (480 nm) up to 10 11 quanta cm −2  s −1 elicited steep increases in FOS mRNA , while increases between 10 12 and 5 × 10 13 quanta  cm −2  s −1 resulted in equally high FOS expression. The HEK‐ hM el cells were used to characterize facets of melanopsin's light‐induced FOS response not approachable in vivo . Novel information such as dependency of the FOS response on both melanopsin amount and light intensity in addition to a detailed time‐course of both FOS mRNA and protein were revealed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here