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Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant
In binocular animals that exhibit stereoscopic visual responses, the axons of retinal ganglion cells (RGCs) connect to brain areas bilaterally by forming a commissure called the optic chiasm (OC). Ventral anterior homeobox 1 (Vax1) contributes to the formation of the OC, acting endogenously in optic...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981622/ https://www.ncbi.nlm.nih.gov/pubmed/36737666 http://dx.doi.org/10.1038/s12276-023-00930-4 |
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author | Min, Kwang Wook Kim, Namsuk Lee, Jae Hoon Sung, Younghoon Kim, Museong Lee, Eun Jung Kim, Jong-Myeong Kim, Jae-Hyun Lee, Jaeyoung Cho, Wonjin Yang, Jee Myung Kim, Nury Kim, Jaehoon Lee, C. Justin Park, Young-Gyun Lee, Seung-Hee Lee, Han-Woong Kim, Jin Woo |
author_facet | Min, Kwang Wook Kim, Namsuk Lee, Jae Hoon Sung, Younghoon Kim, Museong Lee, Eun Jung Kim, Jong-Myeong Kim, Jae-Hyun Lee, Jaeyoung Cho, Wonjin Yang, Jee Myung Kim, Nury Kim, Jaehoon Lee, C. Justin Park, Young-Gyun Lee, Seung-Hee Lee, Han-Woong Kim, Jin Woo |
author_sort | Min, Kwang Wook |
collection | PubMed |
description | In binocular animals that exhibit stereoscopic visual responses, the axons of retinal ganglion cells (RGCs) connect to brain areas bilaterally by forming a commissure called the optic chiasm (OC). Ventral anterior homeobox 1 (Vax1) contributes to the formation of the OC, acting endogenously in optic pathway cells and exogenously in growing RGC axons. Here, we generated Vax1(AA/AA) mice expressing the Vax1(AA) mutant, which is incapable of intercellular transfer. We found that RGC axons cannot take up Vax1(AA) protein from the Vax1(AA/AA) mouse optic stalk (OS) and grow slowly to arrive at the hypothalamus at a late stage. The RGC axons of Vax1(AA/AA) mice connect exclusively to ipsilateral brain areas after failing to access the midline, resulting in reduced visual acuity and abnormal oculomotor responses. Overall, our study provides physiological evidence for the necessity of intercellular transfer of Vax1 and the importance of the bilateral RGC axon projection in proper visuomotor responses. |
format | Online Article Text |
id | pubmed-9981622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99816222023-03-04 Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant Min, Kwang Wook Kim, Namsuk Lee, Jae Hoon Sung, Younghoon Kim, Museong Lee, Eun Jung Kim, Jong-Myeong Kim, Jae-Hyun Lee, Jaeyoung Cho, Wonjin Yang, Jee Myung Kim, Nury Kim, Jaehoon Lee, C. Justin Park, Young-Gyun Lee, Seung-Hee Lee, Han-Woong Kim, Jin Woo Exp Mol Med Article In binocular animals that exhibit stereoscopic visual responses, the axons of retinal ganglion cells (RGCs) connect to brain areas bilaterally by forming a commissure called the optic chiasm (OC). Ventral anterior homeobox 1 (Vax1) contributes to the formation of the OC, acting endogenously in optic pathway cells and exogenously in growing RGC axons. Here, we generated Vax1(AA/AA) mice expressing the Vax1(AA) mutant, which is incapable of intercellular transfer. We found that RGC axons cannot take up Vax1(AA) protein from the Vax1(AA/AA) mouse optic stalk (OS) and grow slowly to arrive at the hypothalamus at a late stage. The RGC axons of Vax1(AA/AA) mice connect exclusively to ipsilateral brain areas after failing to access the midline, resulting in reduced visual acuity and abnormal oculomotor responses. Overall, our study provides physiological evidence for the necessity of intercellular transfer of Vax1 and the importance of the bilateral RGC axon projection in proper visuomotor responses. Nature Publishing Group UK 2023-02-03 /pmc/articles/PMC9981622/ /pubmed/36737666 http://dx.doi.org/10.1038/s12276-023-00930-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Min, Kwang Wook Kim, Namsuk Lee, Jae Hoon Sung, Younghoon Kim, Museong Lee, Eun Jung Kim, Jong-Myeong Kim, Jae-Hyun Lee, Jaeyoung Cho, Wonjin Yang, Jee Myung Kim, Nury Kim, Jaehoon Lee, C. Justin Park, Young-Gyun Lee, Seung-Hee Lee, Han-Woong Kim, Jin Woo Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title | Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title_full | Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title_fullStr | Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title_full_unstemmed | Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title_short | Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant |
title_sort | visuomotor anomalies in achiasmatic mice expressing a transfer-defective vax1 mutant |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981622/ https://www.ncbi.nlm.nih.gov/pubmed/36737666 http://dx.doi.org/10.1038/s12276-023-00930-4 |
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