Journal Article

DZNE-2026-00950

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png The Maintenance of Dysmyelinated Small-Diameter Axons by 14-3-3s in the Central Nervous System.

Yamada, N. ; Saito, H. ; Takahashi, R. ; Fujisato, M. ; Hosoda, Y. ; Sasaki, B. ; Yamada, M. ; Abe, S. ; Hayashi, C. ; Yoshimoto, A. ; Ohkawa, R. ; Matt, T. J. ; M Bareyre, F. ; Berghoff, S.DZNE* ; Simons, M.DZNE* ; Suzuki, N.

2026
Wiley-Liss Bognor Regis [u.a.]

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Please use a persistent id in citations: doi:10.1002/glia.70221

Abstract: In the central nervous system, myelin formed around nerve axons by oligodendrocyte enables efficient conduction of action potentials and maintains axonal homeostasis. Therefore, in demyelinating diseases, such as multiple sclerosis (MS), axonal degeneration and loss, particularly in small-diameter axons, are observed. Teneurin-4 deficient (Ten-4 -/-) mice exhibit severe dysmyelination of small-diameter axons, but survive for over a year. Here, we aimed to elucidate the mechanism of the survival of small-diameter axons without myelin using Ten-4 -/- mice. An immunohistochemical analysis showed abnormally diffused and intense staining of neurofilament. Further, the immunohistochemical signal of nonphosphorylated neurofilament and amyloid precursor protein was higher in Ten-4 -/- mice. An electron microscopy analysis unexpectedly revealed that small-diameter axons in Ten-4 -/- mice survived at the age of 1 year, despite the absence of compact myelin. To elucidate the molecular mechanism, we performed a proteomics analysis in the Ten-4 -/- tissue by mass spectrometry. The result indicated that four of the seven 14-3-3 isoforms were highly expressed in Ten-4 -/- small-diameter axons. Finally, when the function of 14-3-3s in Ten-4 -/- mice was inhibited by 14-3-3 inhibitors, BV02 and difopein, the progression of small-diameter axon damage was observed. Altogether, 14-3-3s are among the pro-survival factors in dysmyelinated small-diameter axons. Our findings may be useful for better understanding the pathogenesis of demyelinating diseases, such as MS, as well as for the development of new treatments.

Keyword(s): Animals (MeSH) ; 14-3-3 Proteins: metabolism (MeSH) ; 14-3-3 Proteins: genetics (MeSH) ; Axons: metabolism (MeSH) ; Axons: pathology (MeSH) ; Axons: ultrastructure (MeSH) ; Myelin Sheath: metabolism (MeSH) ; Myelin Sheath: pathology (MeSH) ; Mice (MeSH) ; Mice, Knockout (MeSH) ; Demyelinating Diseases: pathology (MeSH) ; Demyelinating Diseases: metabolism (MeSH) ; Central Nervous System: metabolism (MeSH) ; Central Nervous System: pathology (MeSH) ; Nerve Tissue Proteins: genetics (MeSH) ; Nerve Tissue Proteins: metabolism (MeSH) ; Nerve Tissue Proteins: deficiency (MeSH) ; Mice, Inbred C57BL (MeSH) ; 14‐3‐3 ; axon ; myelin ; 14-3-3 Proteins ; Nerve Tissue Proteins

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Contributing Institute(s):

1. Molecular Neurobiology (AG Simons)

Research Program(s):

1. 351 - Brain Function (POF4-351) (POF4-351)

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Database coverage:
; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Wiley ; Essential Science Indicators ; IF >= 5 ; JCR ; Nationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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