A role for astrocytes in cerebellar deficits in frataxin deficiency: Protection by insulin-like growth factor I

Franco, C. and Genis, L. and Navarro, J. A. and Perez-Domper, P. and Fernandez, A. M. and Schneuwly, S. and Torres Aleman, I. (2017) A role for astrocytes in cerebellar deficits in frataxin deficiency: Protection by insulin-like growth factor I. MOLECULAR AND CELLULAR NEUROSCIENCE, 80. pp. 100-110. ISSN 1044-7431, 1095-9327

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Abstract

Inherited neurodegenerative diseases such as Friedreich's ataxia (FRDA), produced by deficiency of the mitochondrial chaperone frataxin (Fxn), shows specific neurological deficits involving different subset of neurons even though deficiency of Fxn is ubiquitous. Because astrocytes are involved in neurodegeneration, we analyzed whether they are also affected by frataxin deficiency and contribute to the disease. We also tested whether insulin-like growth factor I (IGF-I), that has proven effective in increasing frataxin levels both in neurons and in astrocytes, also exerts in vivo protective actions. Using the GFAP promoter expressed by multipotential stem cells during development and mostly by astrocytes in the adult, we ablated Fxn in a time-dependent manner in mice (FGKO mice) and found severe ataxia and early death when Fxn was eliminated during development, but not when deleted in the adult. Analysis of underlying mechanisms revealed that Fxn deficiency elicited growth and survival impairments in developing cerebellar astrocytes, whereas forebrain astrocytes grew normally. A similar time-dependent effect of frataxin deficiency in astrocytes was observed in a fly model. In addition, treatment of FGKO mice with IGF-I improved their motor performance, reduced cerebellar atrophy, and increased survival. These observations indicate that a greater vulnerability of developing cerebellar astrocytes to Fxn deficiency may contribute to cerebellar deficits in this inherited disease. Our data also confirm a therapeutic benefit of IGF-I in early FRDA deficiency. (C) 2017 Elsevier Inc. All rights reserved.

Item Type: Article
Uncontrolled Keywords: GAA TRIPLET-REPEAT; FRIEDREICH ATAXIA; GENE-EXPRESSION; TRANSGENIC MICE; MOUSE MODELS; NEURODEGENERATION; EXPANSION; CORTEX; CELLS; CALCINEURIN; Frataxin deficiency; Astrocytes; Brain development; Insulin-like growth factor I
Subjects: 500 Science > 590 Zoological sciences
Divisions: Biology, Preclinical Medicine > Institut für Zoologie > Entwicklungsbiologie (Prof. Dr. Stephan Schneuwly)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 14 Dec 2018 13:11
Last Modified: 19 Feb 2019 12:50
URI: https://pred.uni-regensburg.de/id/eprint/1087

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