Characterization of retinal ganglion cell, horizontal cell, and amacrine cell types expressing the neurotrophic receptor tyrosine kinase Ret.
Characterization of retinal ganglion cell, horizontal cell, and amacrine cell types expressing the neurotrophic receptor tyrosine kinase Ret.
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DOI:
10.1002/cne.24367
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发表时间:
2018-03-01
期刊:
影响因子:
--
通讯作者:
Badea TC
中科院分区:
文献类型:
--
作者:
Parmhans N;Sajgo S;Niu J;Luo W;Badea TC
We report the retinal expression pattern of Ret, a receptor tyrosine kinase for the glial derived neurotrophic factor (GDNF) family ligands (GFLs), during development and in the adult mouse. Ret is initially expressed in retinal ganglion cells (RGCs), followed by horizontal cells (HCs) and amacrine cells (ACs), beginning with the early stages of postmitotic development. Ret expression persists in all three classes of neurons in the adult. Using RNA sequencing, immunostaining and random sparse recombination, we show that Ret is expressed in at least three distinct types of ACs, and ten types of RGCs. Using intersectional genetics, we describe the dendritic arbor morphologies of RGC types expressing Ret in combination with each of the three members of the POU4f/Brn3 family of transcription factors. Ret expression overlaps with Brn3a in 4 RGC types, with Brn3b in 5 RGC types, and with Brn3c in one RGC type, respectively. Ret+ RGCs project to the lateral geniculate nucleus (LGN), pretectal area (PTA) and superior colliculus (SC), and avoid the suprachiasmatic nucleus and accessory optic system. Brn3a+ Ret+ and Brn3c+ Ret+ RGCs project preferentially to contralateral retinorecipient areas, while Brn3b+ Ret+ RGCs shows minor ipsilateral projections to the olivary pretectal nucleus and the LGN. Our findings establish intersectional genetic approaches for the anatomic and developmental characterization of individual Ret+ RGC types. In addition, they provide necessary information for addressing the potential interplay between GDNF neurotrophic signaling and transcriptional regulation in RGC type specification.
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DOI:
10.1523/jneurosci.1218-09.2009
发表时间:
2009-07-01
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Crook JD;Davenport CM;Peterson BB;Packer OS;Detwiler PB;Dacey DM
通讯作者:
Dacey DM
影响因子:
3.7
作者:
Badea TC;Hua ZL;Smallwood PM;Williams J;Rotolo T;Ye X;Nathans J
通讯作者:
Nathans J
DOI:
10.1523/jneurosci.2555-10.2011
发表时间:
2011-05-18
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Cherry TJ;Wang S;Bormuth I;Schwab M;Olson J;Cepko CL
通讯作者:
Cepko CL
影响因子:
5.5
作者:
CLELAND, BG;LEVICK, WR
通讯作者:
LEVICK, WR
影响因子:
64.8
作者:
DACEY, DM;LEE, BB
通讯作者:
LEE, BB