4.7 Article

GDF10 is a signal for axonal sprouting and functional recovery after stroke

Journal

NATURE NEUROSCIENCE
Volume 18, Issue 12, Pages 1737-1745

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nn.4146

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Funding

  1. US National Institutes of Health [NS085019, NS086431]
  2. American Heart Association [09SDG2310180]
  3. Richard Merkin Foundation for Neural Repair at UCLA
  4. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
  5. Edwin W. and Catherine Davis Foundation

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Stroke produces a limited process of neural repair. Axonal sprouting in cortex adjacent to the infarct is part of this recovery process, but the signal that initiates axonal sprouting is not known. Growth and differentiation factor 10 (GDF10) is induced in pen-infarct neurons in mice, non-human primates and humans. GDF10 promotes axonal outgrowth in vitro in mouse, rat and human neurons through TGF beta R1 and TGF beta RII signaling. Using pharmacogenetic gain- and loss-of-function studies, we found that GDF10 produced axonal sprouting and enhanced functional recovery after stroke; knocking down GDF10 blocked axonal sprouting and reduced recovery. RNA sequencing from pen-infarct cortical neurons revealed that GDF10 downregulated PTEN, upregulated PI3 kinase signaling and induced specific axonal guidance molecules. Using unsupervised genome-wide association analysis of the GDF10 transcriptome, we found that it was not related to neurodevelopment, but may partially overlap with other CNS injury patterns. Thus, GDF10 is a stroke-induced signal for axonal sprouting and functional recovery.

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