TY - JOUR
T1 - Microarray analysis of the effect of dexamethasone on murine cochlear explants
AU - Maeda, Yukihide
AU - Fukushima, Kunihiro
AU - Hirai, Misato
AU - Kariya, Shin
AU - Smith, Richard J.H.
AU - Nishizaki, Kazunori
N1 - Funding Information:
This work was supported by a grant from the Ministry of Education, Culture Sports, Science and Technology of Japan (19591969) and in part by the NIH (NIDCD grant DC002842 (R.J.H.S.)). R.J.H.S. is the Sterba Hearing Research Professor, University of Iowa College of Medicine.
PY - 2010/12
Y1 - 2010/12
N2 - Conclusions: The microarray analysis identified 39 genes up- or down-regulated by dexamethasone in the cultured tissue of mice cochlea. Of the eight genes most highly affected, several are suggested to have protective effects in the traumatized inner ear (Fkbp5, Glucocorticoid-induced leucine zipper (Gilz), glutathione peroxidase 3) and for others, a plausible mechanism of action can be offered (claudin 10, glutamate-ammonia ligase). The present data may support the use of dexamethasone to treat acute sensorineural hearing loss. It is warrantable to test these results in the in vivo cochlea. Objectives: To identify genes whose expression is markedly up- or down-regulated by dexamethasone in the cochlear tissue. Methods: Murine cochlear tissue was cultured with or without dexamethasone for 48 h in vitro. The gene expression profiles were compared between the dexamethasone-treated and untreated cochlear tissue using a microarray that covers 33 696 transcripts (24 878 genes) of mice and quantitative real-time RT-PCR. Results: The microarray analysis identified 39 genes that are up- or down-regulated by more than twofold in the presence of dexamethasone in the cochlear culture. Genes up- or down-regulated by at least threefold include Fkbp5, Gilz, glutathione peroxidase 3, claudin 10, glutamate-ammonia ligase, proteoglycan 1, integrin beta-like 1, and alpha subunit of glycoprotein hormone.
AB - Conclusions: The microarray analysis identified 39 genes up- or down-regulated by dexamethasone in the cultured tissue of mice cochlea. Of the eight genes most highly affected, several are suggested to have protective effects in the traumatized inner ear (Fkbp5, Glucocorticoid-induced leucine zipper (Gilz), glutathione peroxidase 3) and for others, a plausible mechanism of action can be offered (claudin 10, glutamate-ammonia ligase). The present data may support the use of dexamethasone to treat acute sensorineural hearing loss. It is warrantable to test these results in the in vivo cochlea. Objectives: To identify genes whose expression is markedly up- or down-regulated by dexamethasone in the cochlear tissue. Methods: Murine cochlear tissue was cultured with or without dexamethasone for 48 h in vitro. The gene expression profiles were compared between the dexamethasone-treated and untreated cochlear tissue using a microarray that covers 33 696 transcripts (24 878 genes) of mice and quantitative real-time RT-PCR. Results: The microarray analysis identified 39 genes that are up- or down-regulated by more than twofold in the presence of dexamethasone in the cochlear culture. Genes up- or down-regulated by at least threefold include Fkbp5, Gilz, glutathione peroxidase 3, claudin 10, glutamate-ammonia ligase, proteoglycan 1, integrin beta-like 1, and alpha subunit of glycoprotein hormone.
KW - Gene expression
KW - Glucocorticoid
KW - Sensorineural hearing loss
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U2 - 10.3109/00016489.2010.498836
DO - 10.3109/00016489.2010.498836
M3 - Article
C2 - 20735180
AN - SCOPUS:78649273104
SN - 0001-6489
VL - 130
SP - 1329
EP - 1334
JO - Acta Oto-Laryngologica
JF - Acta Oto-Laryngologica
IS - 12
ER -