Axon Death Pathways Converge on Axundead to Promote Functional and Structural Axon Disassembly

作者：Neukomm Lukas J^*; Burdett Thomas C; Seeds Andrew M; Hampel Stefanie; Coutinho Budd Jaeda C; Farley Jonathan E; Wong Jack; Karadeniz Yonca B; Osterloh Jeannette M; Sheehan Amy E; Freeman Marc R^*

来源：Neuron, 2017, 95(1): 78-+.

DOI：10.1016/j.neuron.2017.06.031

Axon degeneration is a hallmark of neurodegenerative disease and neural injury. Axotomy activates an intrinsic pro-degenerative axon death signaling cascade involving loss of the NAD(+) biosynthetic enzyme Nmnat/Nmnat2 in axons, activation of dSarm/Sarm1, and subsequent Sarm-dependent depletion of NAD(+). Here we identify Axundead (Axed) as a mediator of axon death. axed mutants suppress axon death in several types of axons for the lifespan of the fly and block the pro-degenerative effects of activated dSarm in vivo. Neurodegeneration induced by loss of the sole fly Nmnat ortholog is also fully blocked by axed, but not dsarm, mutants. Thus, pro-degenerative pathwaysactivatedby dSarm signaling or Nmnat elimination ultimately converge on Axed. Remarkably, severed axons morphologically preserved by axon death pathway mutations remain integrated in circuits and able to elicit complex behaviors after stimulation, indicating that blockade of axon death signaling results in long-term functional preservation of axons.

• 出版日期2017-7-5