» Articles » PMID: 28287632

A Mammalian Nervous-system-specific Plasma Membrane Proteasome Complex That Modulates Neuronal Function

Overview
Date 2017 Mar 14
PMID 28287632
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

In the nervous system, rapidly occurring processes such as neuronal transmission and calcium signaling are affected by short-term inhibition of proteasome function. It is unclear how proteasomes are able to acutely regulate such processes, as this action is inconsistent with their canonical role in proteostasis. Here we describe a mammalian nervous-system-specific membrane proteasome complex that directly and rapidly modulates neuronal function by degrading intracellular proteins into extracellular peptides that can stimulate neuronal signaling. This proteasome complex is closely associated with neuronal plasma membranes, exposed to the extracellular space, and catalytically active. Selective inhibition of the membrane proteasome complex by a cell-impermeable proteasome inhibitor blocked the production of extracellular peptides and attenuated neuronal-activity-induced calcium signaling. Moreover, we observed that membrane-proteasome-derived peptides were sufficient to induce neuronal calcium signaling. Our discoveries challenge the prevailing notion that proteasomes function primarily to maintain proteostasis, and highlight a form of neuronal communication that takes place through a membrane proteasome complex.

Citing Articles

Mechanisms of ubiquitin-independent proteasomal degradation and their roles in age-related neurodegenerative disease.

Church T, Margolis S Front Cell Dev Biol. 2025; 12:1531797.

PMID: 39990094 PMC: 11842346. DOI: 10.3389/fcell.2024.1531797.


Tracking proteasome degradation: A cross-organ analysis via intact degradomics mass spectrometry.

Zittlau K, Zachor-Movshovitz D, Leushkin Y, Schimmel Brener R, Morgenstern D, Ben-Nissan G Proc Natl Acad Sci U S A. 2025; 122(8):e2419607122.

PMID: 39964708 PMC: 11874349. DOI: 10.1073/pnas.2419607122.


Autoantibodies in the Pathogenesis of Podocytopathies.

Blume L, Meyer-Schwesinger C J Am Soc Nephrol. 2025; 36(3):336-338.

PMID: 39883526 PMC: 11888953. DOI: 10.1681/ASN.0000000624.


Localized molecular chaperone synthesis maintains neuronal dendrite proteostasis.

Alecki C, Rizwan J, Le P, Jacob-Tomas S, Comaduran M, Verbrugghe M Nat Commun. 2024; 15(1):10796.

PMID: 39737952 PMC: 11685665. DOI: 10.1038/s41467-024-55055-7.


ProEnd: a comprehensive database for identifying HbYX motif-containing proteins across the tree of life.

Salcedo-Tacuma D, Howells G, McHose C, Gutierrez-Diaz A, Schupp J, Smith D BMC Genomics. 2024; 25(1):951.

PMID: 39396964 PMC: 11475706. DOI: 10.1186/s12864-024-10864-4.


References
1.
Ben-Nissan G, Sharon M . Regulating the 20S proteasome ubiquitin-independent degradation pathway. Biomolecules. 2014; 4(3):862-84. PMC: 4192676. DOI: 10.3390/biom4030862. View

2.
Patel T, Man K, Firestein B, Meaney D . Automated quantification of neuronal networks and single-cell calcium dynamics using calcium imaging. J Neurosci Methods. 2015; 243:26-38. PMC: 5553047. DOI: 10.1016/j.jneumeth.2015.01.020. View

3.
Werner H, Dimou L, Klugmann M, Pfeiffer S, Nave K . Multiple splice isoforms of proteolipid M6B in neurons and oligodendrocytes. Mol Cell Neurosci. 2001; 18(6):593-605. DOI: 10.1006/mcne.2001.1044. View

4.
Pines J, Lindon C . Proteolysis: anytime, any place, anywhere?. Nat Cell Biol. 2005; 7(8):731-5. DOI: 10.1038/ncb0805-731. View

5.
Coux O, Tanaka K, GOLDBERG A . Structure and functions of the 20S and 26S proteasomes. Annu Rev Biochem. 1996; 65:801-47. DOI: 10.1146/annurev.bi.65.070196.004101. View