Tentonin 3 regulates the proliferation and migration of neural stem cells during embryonic brain development

BACKGROUND: Cell fate determination during brain development, encompassing both neural stem cells (NSCs) and immature neurons, is orchestrated by complex mechanical signals. While mechanical sensing during forebrain development is gaining recognition, the underlying regulatory genes remain underexplored. RESULTS: In this study, we present a comprehensive analysis of the expression patterns of the mechanosensitive channel Tentonin 3 (TMEM150C, TTN3) across critical stages of embryonic brain development (E12.5, E14.5, E16.5, and E18.5) using RNAscope technology. We investigated Ttn3 expression in NSCs and immature neurons through co-staining with Nestin, Eomesodermin, and Doublecortin probes. Ttn3 transcripts were detected across multiple embryonic brain regions and layers, with a higher expression in the superficial layers compared to the ventricular and subventricular zones. In addition, we demonstrate that TTN3 is involved in the proliferation and migration of progenitor cells. CONCLUSIONS: Our findings suggest that TTN3 may play a critical role in embryonic brain development, potentially contributing as a mechanotransduction mediator.

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Publication Details

Journal
BMC Biology
Published
2026-04-21
DOI
https://doi.org/10.1186/s12915-026-02604-9
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tentonin 3 regulates the proliferation and migration of neural stem cells during embryonic brain development

Gyu‐Sang Hong, Uhtaek Oh, Kyungmin Kim, Maria Al Nuilati et al.
BMC Biology
Cellular Mechanics and Interactions
article

Tentonin 3 regulates the proliferation and migration of neural stem cells during embryonic brain development

Gyu‐Sang Hong, Uhtaek Oh, Kyungmin Kim, Maria Al Nuilati, Jimin Kang, Min Suk Kim
article en

Abstract

BACKGROUND: Cell fate determination during brain development, encompassing both neural stem cells (NSCs) and immature neurons, is orchestrated by complex mechanical signals. While mechanical sensing during forebrain development is gaining recognition, the underlying regulatory genes remain underexplored. RESULTS: In this study, we present a comprehensive analysis of the expression patterns of the mechanosensitive channel Tentonin 3 (TMEM150C, TTN3) across critical stages of embryonic brain development (E12.5, E14.5, E16.5, and E18.5) using RNAscope technology. We investigated Ttn3 expression in NSCs and immature neurons through co-staining with Nestin, Eomesodermin, and Doublecortin probes. Ttn3 transcripts were detected across multiple embryonic brain regions and layers, with a higher expression in the superficial layers compared to the ventricular and subventricular zones. In addition, we demonstrate that TTN3 is involved in the proliferation and migration of progenitor cells. CONCLUSIONS: Our findings suggest that TTN3 may play a critical role in embryonic brain development, potentially contributing as a mechanotransduction mediator.

BMC Biology
Seoul National University of Science and Technology (KR), Seoul National University (KR), Korea Institute of Brain Science (KR), Korean Association Of Science and Technology Studies (KR), Bio-Medical Science (South Korea) (KR), Korea Institute of Science and Technology (KR), Korea University of Science and Technology (KR)
Korea Institute of Science and Technology, National Research Foundation of Korea
Openalex Percentile: Top 12%
Cellular Mechanics and Interactions
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