TY - JOUR
T1 - Presynaptic partner selection during retinal circuit reassembly varies with timing of neuronal regeneration in vivo
AU - Yoshimatsu, Takeshi
AU - D'Orazi, Florence D.
AU - Gamlin, Clare R.
AU - Suzuki, Sachihiro C.
AU - Suli, Arminda
AU - Kimelman, David
AU - Raible, David W.
AU - Wong, Rachel O.
N1 - Funding Information:
We thank Wong lab members for helpful discussions. This work was supported by the following grants (NIH EY14358 to R.O.W., the Vision Core Grant EY01730 to M. Neitz, Developmental Biology Training Grant HD07183 to F.D.D. and C.R.G., GM079203 to D.K. and DC011269 to D.W.R.).
PY - 2016/2/3
Y1 - 2016/2/3
N2 - Whether neurons can restore their original connectivity patterns during circuit repair is unclear. Taking advantage of the regenerative capacity of zebrafish retina, we show here the remarkable specificity by which surviving neurons reassemble their connectivity upon regeneration of their major input. H3 horizontal cells (HCs) normally avoid red and green cones, and prefer ultraviolet over blue cones. Upon ablation of the major (ultraviolet) input, H3 HCs do not immediately increase connectivity with other cone types. Instead, H3 dendrites retract and re-extend to contact new ultraviolet cones. But, if regeneration is delayed or absent, blue-cone synaptogenesis increases and ectopic synapses are made with red and green cones. Thus, cues directing synapse specificity can be maintained following input loss, but only within a limited time period. Further, we postulate that signals from the major input that shape the H3 HC's wiring pattern during development persist to restrict miswiring after damage.
AB - Whether neurons can restore their original connectivity patterns during circuit repair is unclear. Taking advantage of the regenerative capacity of zebrafish retina, we show here the remarkable specificity by which surviving neurons reassemble their connectivity upon regeneration of their major input. H3 horizontal cells (HCs) normally avoid red and green cones, and prefer ultraviolet over blue cones. Upon ablation of the major (ultraviolet) input, H3 HCs do not immediately increase connectivity with other cone types. Instead, H3 dendrites retract and re-extend to contact new ultraviolet cones. But, if regeneration is delayed or absent, blue-cone synaptogenesis increases and ectopic synapses are made with red and green cones. Thus, cues directing synapse specificity can be maintained following input loss, but only within a limited time period. Further, we postulate that signals from the major input that shape the H3 HC's wiring pattern during development persist to restrict miswiring after damage.
UR - http://www.scopus.com/inward/record.url?scp=84957598061&partnerID=8YFLogxK
U2 - 10.1038/ncomms10590
DO - 10.1038/ncomms10590
M3 - Article
C2 - 26838932
AN - SCOPUS:84957598061
SN - 2041-1723
VL - 7
JO - Nature communications
JF - Nature communications
M1 - 10590
ER -