| Literature DB >> 32531201 |
Chaitali Mukherjee1, Tina Kling2, Belisa Russo3, Kerstin Miebach4, Eva Kess3, Martina Schifferer5, Liliana D Pedro1, Ulrich Weikert2, Maryam K Fard5, Nirmal Kannaiyan6, Moritz Rossner6, Marie-Louise Aicher7, Sandra Goebbels7, Klaus-Armin Nave7, Eva-Maria Krämer-Albers4, Anja Schneider8, Mikael Simons9.
Abstract
An evolutionarily conserved function of glia is to provide metabolic and structural support for neurons. To identify molecules generated by glia and with vital functions for neurons, we used Drosophila melanogaster as a screening tool, and subsequently translated the findings to mice. We found that a cargo receptor operating in the secretory pathway of glia was essential to maintain axonal integrity by regulating iron buffering. Ferritin heavy chain was identified as the critical secretory cargo, required for the protection against iron-mediated ferroptotic axonal damage. In mice, ferritin heavy chain is highly expressed by oligodendrocytes and secreted by employing an unconventional secretion pathway involving extracellular vesicles. Disrupting the release of extracellular vesicles or the expression of ferritin heavy chain in oligodendrocytes causes neuronal loss and oxidative damage in mice. Our data point to a role of oligodendrocytes in providing an antioxidant defense system to support neurons against iron-mediated cytotoxicity.Entities:
Keywords: axon-glia; ferritin; glia; iron; myelin; oligodendrocytes
Year: 2020 PMID: 32531201 PMCID: PMC7116799 DOI: 10.1016/j.cmet.2020.05.019
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287