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A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans
Synaptic positions underlie precise circuit connectivity. Synaptic positions can be established during embryogenesis and sustained during growth. The mechanisms that sustain synaptic specificity during allometric growth are largely unknown. We performed forward genetic screens in C. elegans for regu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164957/ https://www.ncbi.nlm.nih.gov/pubmed/32255430 http://dx.doi.org/10.7554/eLife.55890 |
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author | Fan, Jiale Ji, Tingting Wang, Kai Huang, Jichang Wang, Mengqing Manning, Laura Dong, Xiaohua Shi, Yanjun Zhang, Xumin Shao, Zhiyong Colón-Ramos, Daniel A |
author_facet | Fan, Jiale Ji, Tingting Wang, Kai Huang, Jichang Wang, Mengqing Manning, Laura Dong, Xiaohua Shi, Yanjun Zhang, Xumin Shao, Zhiyong Colón-Ramos, Daniel A |
author_sort | Fan, Jiale |
collection | PubMed |
description | Synaptic positions underlie precise circuit connectivity. Synaptic positions can be established during embryogenesis and sustained during growth. The mechanisms that sustain synaptic specificity during allometric growth are largely unknown. We performed forward genetic screens in C. elegans for regulators of this process and identified mig-17, a conserved ADAMTS metalloprotease. Proteomic mass spectrometry, cell biological and genetic studies demonstrate that MIG-17 is secreted from cells like muscles to regulate basement membrane proteins. In the nematode brain, the basement membrane does not directly contact synapses. Instead, muscle-derived basement membrane coats one side of the glia, while glia contact synapses on their other side. MIG-17 modifies the muscle-derived basement membrane to modulate epidermal-glial crosstalk and sustain glia location and morphology during growth. Glia position in turn sustains the synaptic pattern established during embryogenesis. Our findings uncover a muscle-epidermis-glia signaling axis that sustains synaptic specificity during the organism’s allometric growth. |
format | Online Article Text |
id | pubmed-7164957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71649572020-04-20 A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans Fan, Jiale Ji, Tingting Wang, Kai Huang, Jichang Wang, Mengqing Manning, Laura Dong, Xiaohua Shi, Yanjun Zhang, Xumin Shao, Zhiyong Colón-Ramos, Daniel A eLife Neuroscience Synaptic positions underlie precise circuit connectivity. Synaptic positions can be established during embryogenesis and sustained during growth. The mechanisms that sustain synaptic specificity during allometric growth are largely unknown. We performed forward genetic screens in C. elegans for regulators of this process and identified mig-17, a conserved ADAMTS metalloprotease. Proteomic mass spectrometry, cell biological and genetic studies demonstrate that MIG-17 is secreted from cells like muscles to regulate basement membrane proteins. In the nematode brain, the basement membrane does not directly contact synapses. Instead, muscle-derived basement membrane coats one side of the glia, while glia contact synapses on their other side. MIG-17 modifies the muscle-derived basement membrane to modulate epidermal-glial crosstalk and sustain glia location and morphology during growth. Glia position in turn sustains the synaptic pattern established during embryogenesis. Our findings uncover a muscle-epidermis-glia signaling axis that sustains synaptic specificity during the organism’s allometric growth. eLife Sciences Publications, Ltd 2020-04-07 /pmc/articles/PMC7164957/ /pubmed/32255430 http://dx.doi.org/10.7554/eLife.55890 Text en © 2020, Fan et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Fan, Jiale Ji, Tingting Wang, Kai Huang, Jichang Wang, Mengqing Manning, Laura Dong, Xiaohua Shi, Yanjun Zhang, Xumin Shao, Zhiyong Colón-Ramos, Daniel A A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title_full | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title_fullStr | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title_full_unstemmed | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title_short | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
title_sort | muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in caenorhabditis elegans |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164957/ https://www.ncbi.nlm.nih.gov/pubmed/32255430 http://dx.doi.org/10.7554/eLife.55890 |
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