Developmental decline in neuronal regeneration by the progressive change of two intrinsic timers.
basic_science · Level V
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- Record sourced from PubMed, PMID 23599497.
- Also identified by DOI 10.1126/science.1231321 and PMC identifier 4074024.
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Abstract
Like mammalian neurons, Caenorhabditis elegans neurons lose axon regeneration ability as they age, but it is not known why. Here, we report that let-7 contributes to a developmental decline in anterior ventral microtubule (AVM) axon regeneration. In older AVM axons, let-7 inhibits regeneration by down-regulating LIN-41, an important AVM axon regeneration-promoting factor. Whereas let-7 inhibits lin-41 expression in older neurons through the lin-41 3' untranslated region, lin-41 inhibits let-7 expression in younger neurons through Argonaute ALG-1. This reciprocal inhibition ensures that axon regeneration is inhibited only in older neurons. These findings show that a let-7-lin-41 regulatory circuit, which was previously shown to control timing of events in mitotic stem cell lineages, is reutilized in postmitotic neurons to control postdifferentiation events.
Medical subject headings
- Axons
- Caenorhabditis elegans
- Caenorhabditis elegans Proteins
- MicroRNAs
- Nerve Regeneration
- Neurons
- Transcription Factors