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Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells

The ectopic distribution of synaptic ribbons in dendrites of mouse retinal bipolar cells was examined by using genetic ablation of metabotropic glutamate receptor subtype 6 (mGluR6), electron microscopy, and immunocytochemistry. Ectopic ribbons were observed in dendrites of rod and ON-cone bipolar c...

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Autores principales: Ishii, Masaaki, Morigiwa, Katsuko, Takao, Motoharu, Nakanishi, Shigetada, Fukuda, Yutaka, Mimura, Osamu, Tsukamoto, Yoshihiko
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779389/
https://www.ncbi.nlm.nih.gov/pubmed/19859741
http://dx.doi.org/10.1007/s00441-009-0880-0
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author Ishii, Masaaki
Morigiwa, Katsuko
Takao, Motoharu
Nakanishi, Shigetada
Fukuda, Yutaka
Mimura, Osamu
Tsukamoto, Yoshihiko
author_facet Ishii, Masaaki
Morigiwa, Katsuko
Takao, Motoharu
Nakanishi, Shigetada
Fukuda, Yutaka
Mimura, Osamu
Tsukamoto, Yoshihiko
author_sort Ishii, Masaaki
collection PubMed
description The ectopic distribution of synaptic ribbons in dendrites of mouse retinal bipolar cells was examined by using genetic ablation of metabotropic glutamate receptor subtype 6 (mGluR6), electron microscopy, and immunocytochemistry. Ectopic ribbons were observed in dendrites of rod and ON-cone bipolar cells in the mGluR6-deficient mouse but not in those of wild-type mice. The number of rod spherules facing the ectopic ribbons in mGluR6-deficient rod bipolar dendrites increased gradually during early growth and reached a plateau level of about 20% at 12 weeks. These ectopic ribbons were immunopositive for RIBEYE, a ribbon-specific protein, but the associated vesicles were immunonegative for synaptophysin, a synaptic-vesicle-specific protein. The presence of ectopic ribbons was correlated with an increase in the roundness of the invaginating dendrites of the rod bipolar cells. We further confirmed ectopic ribbons in dendrites of OFF-cone bipolar cells in wild-type retinas. Of the four types of OFF-cone bipolar cells (T1–T4), only the T2-type, which had a greater number of synaptic ribbons at the axon terminal and a thicker axon cylinder than the other types, had ectopic ribbons. Light-adapted experiments revealed that, in wild-type mice under enhanced-light adaptation (considered similar to the mGluR6-deficient state), the roundness in the invaginating dendrites and axon terminals of rod bipolar cells increased, but no ectopic ribbons were detected. Based on these findings and known mechanisms for neurotransmitter release and protein trafficking, the possible mechanisms underlying the ectopic ribbons are discussed on the basis of intracellular transport for the replenishment of synaptic proteins.
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spelling pubmed-27793892009-11-23 Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells Ishii, Masaaki Morigiwa, Katsuko Takao, Motoharu Nakanishi, Shigetada Fukuda, Yutaka Mimura, Osamu Tsukamoto, Yoshihiko Cell Tissue Res Regular Article The ectopic distribution of synaptic ribbons in dendrites of mouse retinal bipolar cells was examined by using genetic ablation of metabotropic glutamate receptor subtype 6 (mGluR6), electron microscopy, and immunocytochemistry. Ectopic ribbons were observed in dendrites of rod and ON-cone bipolar cells in the mGluR6-deficient mouse but not in those of wild-type mice. The number of rod spherules facing the ectopic ribbons in mGluR6-deficient rod bipolar dendrites increased gradually during early growth and reached a plateau level of about 20% at 12 weeks. These ectopic ribbons were immunopositive for RIBEYE, a ribbon-specific protein, but the associated vesicles were immunonegative for synaptophysin, a synaptic-vesicle-specific protein. The presence of ectopic ribbons was correlated with an increase in the roundness of the invaginating dendrites of the rod bipolar cells. We further confirmed ectopic ribbons in dendrites of OFF-cone bipolar cells in wild-type retinas. Of the four types of OFF-cone bipolar cells (T1–T4), only the T2-type, which had a greater number of synaptic ribbons at the axon terminal and a thicker axon cylinder than the other types, had ectopic ribbons. Light-adapted experiments revealed that, in wild-type mice under enhanced-light adaptation (considered similar to the mGluR6-deficient state), the roundness in the invaginating dendrites and axon terminals of rod bipolar cells increased, but no ectopic ribbons were detected. Based on these findings and known mechanisms for neurotransmitter release and protein trafficking, the possible mechanisms underlying the ectopic ribbons are discussed on the basis of intracellular transport for the replenishment of synaptic proteins. Springer-Verlag 2009-10-27 2009 /pmc/articles/PMC2779389/ /pubmed/19859741 http://dx.doi.org/10.1007/s00441-009-0880-0 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Regular Article
Ishii, Masaaki
Morigiwa, Katsuko
Takao, Motoharu
Nakanishi, Shigetada
Fukuda, Yutaka
Mimura, Osamu
Tsukamoto, Yoshihiko
Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title_full Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title_fullStr Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title_full_unstemmed Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title_short Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells
title_sort ectopic synaptic ribbons in dendrites of mouse retinal on- and off-bipolar cells
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779389/
https://www.ncbi.nlm.nih.gov/pubmed/19859741
http://dx.doi.org/10.1007/s00441-009-0880-0
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