TY - JOUR
T1 - Optical control of erk and akt signaling promotes axon regeneration and functional recovery of pns and cns in drosophila
AU - Wang, Qin
AU - Fan, Huaxun
AU - Li, Feng
AU - Skeeters, Savanna S.
AU - Krishnamurthy, Vishnu V.
AU - Song, Yuanquan
AU - Zhang, Kai
N1 - Funding Information:
This work was supported by NIH grants 1R01NS107392 (YS) and 1R01GM132438 (KZ).
PY - 2020/10
Y1 - 2020/10
N2 - Neuroregeneration is a dynamic process synergizing the functional outcomes of multiple signaling circuits. Channelrhodopsin-based optogenetics shows the feasibility of stimulating neural repair but does not pin down specific signaling cascades. Here, we utilized optogenetic systems, optoRaf and optoAKT, to delineate the contribution of the ERK and AKT signaling pathways to neuroregeneration in live Drosophila larvae. We showed that optoRaf or optoAKT activation not only enhanced axon regeneration in both regeneration-competent and-incompetent sensory neurons in the peripheral nervous system but also allowed temporal tuning and proper guidance of axon regrowth. Furthermore, optoRaf and optoAKT differ in their signaling kinetics during regeneration, showing a gated versus graded response, respectively. Importantly in the central nervous system, their activation promotes axon regrowth and functional recovery of the thermonociceptive behavior. We conclude that non-neuronal optogenetics targets damaged neurons and signaling subcircuits, providing a novel strategy in the intervention of neural damage with improved precision.
AB - Neuroregeneration is a dynamic process synergizing the functional outcomes of multiple signaling circuits. Channelrhodopsin-based optogenetics shows the feasibility of stimulating neural repair but does not pin down specific signaling cascades. Here, we utilized optogenetic systems, optoRaf and optoAKT, to delineate the contribution of the ERK and AKT signaling pathways to neuroregeneration in live Drosophila larvae. We showed that optoRaf or optoAKT activation not only enhanced axon regeneration in both regeneration-competent and-incompetent sensory neurons in the peripheral nervous system but also allowed temporal tuning and proper guidance of axon regrowth. Furthermore, optoRaf and optoAKT differ in their signaling kinetics during regeneration, showing a gated versus graded response, respectively. Importantly in the central nervous system, their activation promotes axon regrowth and functional recovery of the thermonociceptive behavior. We conclude that non-neuronal optogenetics targets damaged neurons and signaling subcircuits, providing a novel strategy in the intervention of neural damage with improved precision.
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U2 - 10.7554/eLife.57395
DO - 10.7554/eLife.57395
M3 - Article
C2 - 33021199
SN - 2050-084X
VL - 9
SP - 1
EP - 29
JO - eLife
JF - eLife
M1 - e57395
ER -