TY - JOUR
T1 - Developmental Coordination during Olfactory Circuit Remodeling in Drosophila
AU - Mayseless, Oded
AU - Berns, Dominic S.
AU - Yu, Xiaomeng M.
AU - Riemensperger, Thomas
AU - Fiala, Andre
AU - Schuldiner, Oren
N1 - We thank A.S. Chiang, G. Miesenböck, G.M. Rubin, and the Kyoto (DGRC) and Bloomington Stock Centers for reagents. We thank Chris Potter for providing us with the QUAS-TNT and QUAS-Kir2.1 transgenic lines, O. Golani for assistance with image analysis, and R. Rotkopf for help with statistical analysis. We thank A. Yaron and the members of the Schuldiner lab—especially I. Alyagor, B. Bornstein, and S. Yaniv—for discussions and critical readings of the manuscript. Monoclonal antibodies were obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by the University of Iowa. D.S.B. and X.M.Y. were supported by L. Luo at Stanford university and HHMI during the initial stages of this study. This work was supported by Volkswagen Stiftung (joint Lower Saxony – Israel) grant #A112379 to A.F., T.R., and O.S.; the Israel Science Foundation (ISF) grant #1100/16 to O.S.; a European Research Council (ERC), consolidator grant “AxonGrowth” to O.S.; and an EMBO short term fellowship #382-2016 to O.M. Fly food for this project was funded by the Women Health Research Center.
PY - 2018/9/19
Y1 - 2018/9/19
N2 - Developmental neuronal remodeling is crucial for proper wiring of the adult nervous system. While remodeling of individual neuronal populations has been studied, how neuronal circuits remodel—and whether remodeling of synaptic partners is coordinated—is unknown. We found that the Drosophila anterior paired lateral (APL) neuron undergoes stereotypic remodeling during metamorphosis in a similar time frame as the mushroom body (MB) ɣ-neurons, with whom it forms a functional circuit. By simultaneously manipulating both neuronal populations, we found that cell-autonomous inhibition of ɣ-neuron pruning resulted in the inhibition of APL pruning in a process that is mediated, at least in part, by Ca 2+-Calmodulin and neuronal activity dependent interaction. Finally, ectopic unpruned MB ɣ axons display ectopic connections with the APL, as well as with other neurons, at the adult, suggesting that inhibiting remodeling of one neuronal type can affect the functional wiring of the entire micro-circuit. Developmental remodeling is crucial for stereotypic neural circuit formation. Mayseless et al. describe a neural circuit in Drosophila that undergoes coordinated remodeling. They show that neurons within the same circuit interact via neuronal activity and Ca 2+/Calmodulin signaling to coordinate remodeling.
AB - Developmental neuronal remodeling is crucial for proper wiring of the adult nervous system. While remodeling of individual neuronal populations has been studied, how neuronal circuits remodel—and whether remodeling of synaptic partners is coordinated—is unknown. We found that the Drosophila anterior paired lateral (APL) neuron undergoes stereotypic remodeling during metamorphosis in a similar time frame as the mushroom body (MB) ɣ-neurons, with whom it forms a functional circuit. By simultaneously manipulating both neuronal populations, we found that cell-autonomous inhibition of ɣ-neuron pruning resulted in the inhibition of APL pruning in a process that is mediated, at least in part, by Ca 2+-Calmodulin and neuronal activity dependent interaction. Finally, ectopic unpruned MB ɣ axons display ectopic connections with the APL, as well as with other neurons, at the adult, suggesting that inhibiting remodeling of one neuronal type can affect the functional wiring of the entire micro-circuit. Developmental remodeling is crucial for stereotypic neural circuit formation. Mayseless et al. describe a neural circuit in Drosophila that undergoes coordinated remodeling. They show that neurons within the same circuit interact via neuronal activity and Ca 2+/Calmodulin signaling to coordinate remodeling.
UR - http://www.scopus.com/inward/record.url?scp=85056658940&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.neuron.2018.07.050
DO - https://doi.org/10.1016/j.neuron.2018.07.050
M3 - مقالة
SN - 0896-6273
VL - 99
SP - 1204
EP - 1215
JO - Neuron
JF - Neuron
IS - 6
ER -