Cargando…
Proteomic screen reveals diverse protein transport between connected neurons in the visual system
Intercellular transfer of toxic proteins between neurons is thought to contribute to neurodegenerative disease, but whether direct interneuronal protein transfer occurs in the healthy brain is not clear. To assess the prevalence and identity of transferred proteins and the cellular specificity of tr...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906846/ https://www.ncbi.nlm.nih.gov/pubmed/35081342 http://dx.doi.org/10.1016/j.celrep.2021.110287 |
_version_ | 1784665475120103424 |
---|---|
author | Schiapparelli, Lucio M. Sharma, Pranav He, Hai-Yan Li, Jianli Shah, Sahil H. McClatchy, Daniel B. Ma, Yuanhui Liu, Han-Hsuan Goldberg, Jeffrey L. Yates, John R. Cline, Hollis T. |
author_facet | Schiapparelli, Lucio M. Sharma, Pranav He, Hai-Yan Li, Jianli Shah, Sahil H. McClatchy, Daniel B. Ma, Yuanhui Liu, Han-Hsuan Goldberg, Jeffrey L. Yates, John R. Cline, Hollis T. |
author_sort | Schiapparelli, Lucio M. |
collection | PubMed |
description | Intercellular transfer of toxic proteins between neurons is thought to contribute to neurodegenerative disease, but whether direct interneuronal protein transfer occurs in the healthy brain is not clear. To assess the prevalence and identity of transferred proteins and the cellular specificity of transfer, we biotinylated retinal ganglion cell proteins in vivo and examined biotinylated proteins transported through the rodent visual circuit using microscopy, biochemistry, and mass spectrometry. Electron microscopy demonstrated preferential transfer of biotinylated proteins from retinogeniculate inputs to excitatory lateral geniculate nucleus (LGN) neurons compared with GABAergic neurons. An unbiased mass spectrometry-based screen identified 200 transneuronally transported proteins (TNTPs) isolated from the visual cortex. The majority of TNTPs are present in neuronal exosomes, and virally expressed TNTPs, including tau and β-synuclein, were detected in isolated exosomes and postsynaptic neurons. Our data demonstrate transfer of diverse endogenous proteins between neurons in the healthy intact brain and suggest that TNTP transport may be mediated by exosomes. |
format | Online Article Text |
id | pubmed-8906846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-89068462022-03-09 Proteomic screen reveals diverse protein transport between connected neurons in the visual system Schiapparelli, Lucio M. Sharma, Pranav He, Hai-Yan Li, Jianli Shah, Sahil H. McClatchy, Daniel B. Ma, Yuanhui Liu, Han-Hsuan Goldberg, Jeffrey L. Yates, John R. Cline, Hollis T. Cell Rep Article Intercellular transfer of toxic proteins between neurons is thought to contribute to neurodegenerative disease, but whether direct interneuronal protein transfer occurs in the healthy brain is not clear. To assess the prevalence and identity of transferred proteins and the cellular specificity of transfer, we biotinylated retinal ganglion cell proteins in vivo and examined biotinylated proteins transported through the rodent visual circuit using microscopy, biochemistry, and mass spectrometry. Electron microscopy demonstrated preferential transfer of biotinylated proteins from retinogeniculate inputs to excitatory lateral geniculate nucleus (LGN) neurons compared with GABAergic neurons. An unbiased mass spectrometry-based screen identified 200 transneuronally transported proteins (TNTPs) isolated from the visual cortex. The majority of TNTPs are present in neuronal exosomes, and virally expressed TNTPs, including tau and β-synuclein, were detected in isolated exosomes and postsynaptic neurons. Our data demonstrate transfer of diverse endogenous proteins between neurons in the healthy intact brain and suggest that TNTP transport may be mediated by exosomes. 2022-01-25 /pmc/articles/PMC8906846/ /pubmed/35081342 http://dx.doi.org/10.1016/j.celrep.2021.110287 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license. |
spellingShingle | Article Schiapparelli, Lucio M. Sharma, Pranav He, Hai-Yan Li, Jianli Shah, Sahil H. McClatchy, Daniel B. Ma, Yuanhui Liu, Han-Hsuan Goldberg, Jeffrey L. Yates, John R. Cline, Hollis T. Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title | Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title_full | Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title_fullStr | Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title_full_unstemmed | Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title_short | Proteomic screen reveals diverse protein transport between connected neurons in the visual system |
title_sort | proteomic screen reveals diverse protein transport between connected neurons in the visual system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906846/ https://www.ncbi.nlm.nih.gov/pubmed/35081342 http://dx.doi.org/10.1016/j.celrep.2021.110287 |
work_keys_str_mv | AT schiapparelliluciom proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT sharmapranav proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT hehaiyan proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT lijianli proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT shahsahilh proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT mcclatchydanielb proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT mayuanhui proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT liuhanhsuan proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT goldbergjeffreyl proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT yatesjohnr proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem AT clinehollist proteomicscreenrevealsdiverseproteintransportbetweenconnectedneuronsinthevisualsystem |