Transmembrane semaphorin signalling controls laminar stratification in the mammalian retina (original) (raw)
- Letter
- Published: 10 February 2011
- Kim T. Nguyen-Ba-Charvet4,5,6,
- Aijaz Parray4,5,6,
- Tudor C. Badea2,3 nAff7,
- Alain Chédotal4,5,6 &
- …
- Alex L. Kolodkin1,3
Nature volume 470, pages 259–263 (2011)Cite this article
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Abstract
In the vertebrate retina, establishment of precise synaptic connections among distinct retinal neuron cell types is critical for processing visual information and for accurate visual perception. Retinal ganglion cells (RGCs), amacrine cells and bipolar cells establish stereotypic neurite arborization patterns to form functional neural circuits in the inner plexiform layer (IPL)1,2,3, a laminar region that is conventionally divided into five major parallel sublaminae1,2. However, the molecular mechanisms governing distinct retinal subtype targeting to specific sublaminae within the IPL remain to be elucidated. Here we show that the transmembrane semaphorin Sema6A signals through its receptor PlexinA4 (PlexA4) to control lamina-specific neuronal stratification in the mouse retina. Expression analyses demonstrate that Sema6A and PlexA4 proteins are expressed in a complementary fashion in the developing retina: Sema6A in most ON sublaminae and PlexA4 in OFF sublaminae of the IPL. Mice with null mutations in PlexA4 or Sema6A exhibit severe defects in stereotypic lamina-specific neurite arborization of tyrosine hydroxylase (TH)-expressing dopaminergic amacrine cells, intrinsically photosensitive RGCs (ipRGCs) and calbindin-positive cells in the IPL. Sema6A and PlexA4 genetically interact in vivo for the regulation of dopaminergic amacrine cell laminar targeting. Therefore, neuronal targeting to subdivisions of the IPL in the mammalian retina is directed by repulsive transmembrane guidance cues present on neuronal processes.
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10 February 2011
Three labels were corrected in Fig. 4.
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Acknowledgements
We thank K.-W. Yau for the C-terminal melanopsin antibody, F. Suto for the PlexA4 antibody, B. Howell for the Dab-1 antibody, Y. Yoshida for the _PlexA1_−/− eyes, P. Mombaerts for the _PlexB1_−/− and _PlexB3_−/− mice (unpublished), C. Gu for the PlexD1 -/flox ;nestin cre (unpublished) eyes and M. Tessier-Lavigne for the _PlexA4_−/− mice. We also thank J. Nathans, S. Hattar, K. Mandai and M. Riccomagno for comments on the manuscript and discussions, and members of the Kolodkin laboratory for assistance. This work was supported by R01 NS35165 to A.L.K., a predoctoral fellowship from the Nakajima Foundation to R.L.M., the Fondation pour la Recherche Médicale (Programme équipe FRM) to A.C., the Fondation Retina France to K.T.N.-B.-C., and a PhD fellowship from the Paris School of Neuroscience (ENP) to A.P. A.L.K. is an investigator of the Howard Hughes Medical Institute.
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Author notes
- Tudor C. Badea
Present address: Present address: Retinal Circuit Development & Genetics Unit, Neurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, Bethesda, Maryland 20892, USA .,
Authors and Affiliations
- The Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, 21205, Maryland, USA
Ryota L. Matsuoka & Alex L. Kolodkin - Department of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, 21205, Maryland, USA
Tudor C. Badea - Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, 21205, Maryland, USA
Ryota L. Matsuoka, Tudor C. Badea & Alex L. Kolodkin - Institut National de la Santé et de la Recherche Médicale (INSERM), UMR S968, Institut de la Vision, F-75012 Paris, France ,
Kim T. Nguyen-Ba-Charvet, Aijaz Parray & Alain Chédotal - Université Pierre et Marie Curie (UPMC) Paris VI, UMR S968, Institut de la Vision, F-75012 Paris, France ,
Kim T. Nguyen-Ba-Charvet, Aijaz Parray & Alain Chédotal - Centre National de la Recherche Scientifique (CNRS) UMR 7210, Institut de la Vision, F-75012 Paris, France ,
Kim T. Nguyen-Ba-Charvet, Aijaz Parray & Alain Chédotal
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Contributions
R.L.M., A.C. and A.L.K. conceived and designed the experiments; R.L.M. performed most of the experiments and data analysis; K.T.N.-B.-C., A.P. and A.C. participated in the phenotypic analyses of Sema6A mutant mice and provided _PlexA2_−/− and _PlexB2_−/− mutants; T.C.B. performed cholera toxin injections and provided suggestions and reagents; R.L.M. and A.L.K. wrote the paper.
Corresponding author
Correspondence toAlex L. Kolodkin.
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The authors declare no competing financial interests.
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Matsuoka, R., Nguyen-Ba-Charvet, K., Parray, A. et al. Transmembrane semaphorin signalling controls laminar stratification in the mammalian retina.Nature 470, 259–263 (2011). https://doi.org/10.1038/nature09675
- Received: 03 September 2010
- Revised: 17 November 2010
- Accepted: 26 January 2011
- Published: 10 February 2011
- Issue Date: 10 February 2011
- DOI: https://doi.org/10.1038/nature09675
Editorial Summary
Molecular cue in the developing retina
The retina is a laminated structure made up of several different cellular subtypes, interconnected according to a precise architecture that is vital for proper visual perception. Matsuoka et al. shed new light on the molecular mechanisms governing the development of these circuits. Transmembrane molecules — typically most active as repulsive signals during axonal guidance — exhibit specific expression patterns within the retina that promote appropriate connectivity between cell types. Mutant mice lacking specific isoforms of these semaphorin or plexin molecular families display significant defects in retinal circuitry. Thus, repulsive cues present on the neuronal processes themselves drive proper wiring between lamina within the retina.