Expression of Hypoxia-inducible Factor-1 in the Cochlea of Newborn Rats
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Hypoxia/ischemia is a major pathogenetic factor in the development of hearing loss. An important transcription factor involved in the signaling and adaptation to hypoxia/ischemia is the hypoxia-inducible factor-1 (HIF-1). To study HIF-1 expression we used an in vitro hypoxia model of explant and dissociated cultures of the stria vascularis, the organ of Corti with limbus and the modiolus from the cochlea of 3-5-day-old Wistar rats. Hypoxia differentially increased HIF-1 activity as measured by a reporter gene. Twenty-four hour hypoxia increased HIF-1 activity 14.1+/-3.5-fold in the modiolus, 9.4+/-3.0-fold in the organ of Corti with limbus, and 6.4+/-1.5-fold in the stria vascularis. The HIF-1alpha mRNA level was measured by quantitative reverse transcription polymerase chain reaction and showed a lower expression in the modiolus (1.3+/-0.2 pg/microg RNA) than in both the organ of Corti with limbus and the stria vascularis (2.7-3.2+/-1.3, P<0.01). Hypoxia had no effect on the HIF-1alpha mRNA levels. The region-specific regulation of HIF-1 expression on the transcriptional and posttranslational levels may expand the possibilities for adaptation of the cochlea to hypoxia.
Liang S, Dong S, Liu W, Wang M, Tian S, Ai Y Front Mol Biosci. 2022; 8:806650.
PMID: 35096971 PMC: 8790562. DOI: 10.3389/fmolb.2021.806650.
Chang D, Brown Q, Tsui G, He Y, Liu J, Shi L Brain Sci. 2021; 11(7).
PMID: 34356178 PMC: 8304335. DOI: 10.3390/brainsci11070944.
Qiu J, Singh P, Pan G, De Paolis A, Champagne F, Liu J PLoS One. 2020; 15(8):e0237933.
PMID: 32822407 PMC: 7442246. DOI: 10.1371/journal.pone.0237933.
[Molecular networks of hypoxia and neuronal apoptosis in the cochlea].
Gross J, Olze H, Mazurek B HNO. 2018; 66(9):677-685.
PMID: 30043174 DOI: 10.1007/s00106-018-0539-9.
Direct phosphorylation events involved in HIF-α regulation: the role of GSK-3β.
Mennerich D, Dimova E, Kietzmann T Hypoxia (Auckl). 2014; 2:35-45.
PMID: 27774465 PMC: 5045055. DOI: 10.2147/HP.S60703.