E-MEXP-3786 - Transcription profiling by array of mouse male retinas to investugate IGF-I-induced chronic gliosis and retinal stress

Released on 1 August 2013, last updated on 19 October 2015
Mus musculus
Samples (6)
Array (1)
Protocols (5)
IGF-I exert multiple effects in different retinal cell populations in both physiological and pathological conditions. Transgenic mice overexpressing IGF-I in the retina showed impaired electroretinographic responses at 6-7 months of age that worsen with age. This retinal neuronal dysfunction was correlated with the loss of rod photoreceptors, bipolar, ganglion and amacrines cells. Neuronal alterations were preceded by the overexpression of retinal stress markers, acute phase proteins and gliosis-related genes. IGF-I overexpression leads to chronic gliosis and microgliosis in TgIGF-I retinas, with mild oxidative stress, impaired recycling of glutamate and defective potassium buffering. These impaired supportive functions can contribute to neurodegeneration in TgIGF-I retinas, together with the increased production of pro-inflammatory cytokines, potential mediators of neuronal death.
Experiment types
transcription profiling by array, co-expression, genetic modification, replicate
Insulin-like Growth Factor 2 Overexpression Induces β-Cell Dysfunction and Increases Beta-cell Susceptibility to Damage. Casellas A, Mallol C, Salavert A, Jimenez V, Garcia M, Agudo J, Obach M, Haurigot V, Vilà L, Molas M, Lage R, Morró M, Casana E, Ruberte J, Bosch F. , Europe PMC 25971976
Investigation descriptionE-MEXP-3786.idf.txt
Sample and data relationshipE-MEXP-3786.sdrf.txt
Raw data (1)E-MEXP-3786.raw.1.zip
Array designA-AFFY-36.adf.txt