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Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression

While the role of barrier function in establishing a protective, nutrient-rich, and ionically balanced environment for neurons has been appreciated for some time, little is known about how signaling cues originating in barrier-forming cells participate in maintaining barrier function and influence s...

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Autores principales: Calderon, Mario R., Mori, Megumi, Kauwe, Grant, Farnsworth, Jill, Ulian-Benitez, Suzana, Maksoud, Elie, Shore, Jordan, Haghighi, A. Pejmun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407389/
https://www.ncbi.nlm.nih.gov/pubmed/35969789
http://dx.doi.org/10.1073/pnas.2110097119
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author Calderon, Mario R.
Mori, Megumi
Kauwe, Grant
Farnsworth, Jill
Ulian-Benitez, Suzana
Maksoud, Elie
Shore, Jordan
Haghighi, A. Pejmun
author_facet Calderon, Mario R.
Mori, Megumi
Kauwe, Grant
Farnsworth, Jill
Ulian-Benitez, Suzana
Maksoud, Elie
Shore, Jordan
Haghighi, A. Pejmun
author_sort Calderon, Mario R.
collection PubMed
description While the role of barrier function in establishing a protective, nutrient-rich, and ionically balanced environment for neurons has been appreciated for some time, little is known about how signaling cues originating in barrier-forming cells participate in maintaining barrier function and influence synaptic activity. We have identified Delta/Notch signaling in subperineurial glia (SPG), a crucial glial type for Drosophila motor axon ensheathment and the blood–brain barrier, to be essential for controlling the expression of matrix metalloproteinase 1 (Mmp1), a major regulator of the extracellular matrix (ECM). Our genetic analysis indicates that Delta/Notch signaling in SPG exerts an inhibitory control on Mmp1 expression. In the absence of this inhibition, abnormally enhanced Mmp1 activity disrupts septate junctions and glial ensheathment of peripheral motor nerves, compromising neurotransmitter release at the neuromuscular junction (NMJ). Temporally controlled and cell type–specific transgenic analysis shows that Delta/Notch signaling inhibits transcription of Mmp1 by inhibiting c-Jun N-terminal kinase (JNK) signaling in SPG. Our results provide a mechanistic insight into the regulation of neuronal health and function via glial-initiated signaling and open a framework for understanding the complex relationship between ECM regulation and the maintenance of barrier function.
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spelling pubmed-94073892022-08-26 Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression Calderon, Mario R. Mori, Megumi Kauwe, Grant Farnsworth, Jill Ulian-Benitez, Suzana Maksoud, Elie Shore, Jordan Haghighi, A. Pejmun Proc Natl Acad Sci U S A Biological Sciences While the role of barrier function in establishing a protective, nutrient-rich, and ionically balanced environment for neurons has been appreciated for some time, little is known about how signaling cues originating in barrier-forming cells participate in maintaining barrier function and influence synaptic activity. We have identified Delta/Notch signaling in subperineurial glia (SPG), a crucial glial type for Drosophila motor axon ensheathment and the blood–brain barrier, to be essential for controlling the expression of matrix metalloproteinase 1 (Mmp1), a major regulator of the extracellular matrix (ECM). Our genetic analysis indicates that Delta/Notch signaling in SPG exerts an inhibitory control on Mmp1 expression. In the absence of this inhibition, abnormally enhanced Mmp1 activity disrupts septate junctions and glial ensheathment of peripheral motor nerves, compromising neurotransmitter release at the neuromuscular junction (NMJ). Temporally controlled and cell type–specific transgenic analysis shows that Delta/Notch signaling inhibits transcription of Mmp1 by inhibiting c-Jun N-terminal kinase (JNK) signaling in SPG. Our results provide a mechanistic insight into the regulation of neuronal health and function via glial-initiated signaling and open a framework for understanding the complex relationship between ECM regulation and the maintenance of barrier function. National Academy of Sciences 2022-08-15 2022-08-23 /pmc/articles/PMC9407389/ /pubmed/35969789 http://dx.doi.org/10.1073/pnas.2110097119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Calderon, Mario R.
Mori, Megumi
Kauwe, Grant
Farnsworth, Jill
Ulian-Benitez, Suzana
Maksoud, Elie
Shore, Jordan
Haghighi, A. Pejmun
Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title_full Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title_fullStr Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title_full_unstemmed Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title_short Delta/Notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
title_sort delta/notch signaling in glia maintains motor nerve barrier function and synaptic transmission by controlling matrix metalloproteinase expression
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407389/
https://www.ncbi.nlm.nih.gov/pubmed/35969789
http://dx.doi.org/10.1073/pnas.2110097119
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