Skip to content
Preprint via Europe PMC

<i>Phosphatidylinositol Transfer Protein-1</i> Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in <i>Caenorhabditis elegans</i>

Lin Y, Liao Y, Liao S, Lin T, Shanmugam MM, Hsu P, Chen C, Ching T, Wagner OI, Yuh C, Wang H.

· 2025

Abstract

<h4>Background</h4> Phosphatidylinositol transfer protein-1 ( pitp-1 ) is involved in phosphoinositide turnover. The role of pitp-1 in promoting healthy longevity remains unknown. Our previous work showed that the phosphoinositide turnover genes dagl-1 and dgk-5 regulates lifespan, as overexpression of dagl-1 or knockdown of dgk-5 prolongs lifespan and enhances oxidative stress resistance through TOR signaling. As pitp-1 is a key component of this pathway, we investigated its role in lifespan regulation and the underlying mechanisms, aiming to clarify whether it represents a critical regulator of healthy longevity and how it coordinates conserved signaling pathways to regulate aging. <h4>Methods</h4> C. elegans mutants, RNAi-mediated knockdown, and transgenic overexpression were applied to assess lifespan, motility, stress resistance. Temporal and tissue-specific RNAi were applied to identify the critical time window and tissue for pitp-1 -mediated lifespan regulation. TOR signaling was measured by phosphorylated S6 kinase and puromycin incorporation, and transcriptomic analysis identified affected pathways. <h4>Results</h4> pitp-1 negatively regulates lifespan and healthspan(definition) in Caenorhabditis elegans . Genetic deletion or RNAi-mediated knockdown of pitp-1 extends lifespan, attenuates age-related motility decline, and increases oxidative stress resistance. Temporal and spatial analyses reveal that suppression of pitp-1 in neurons during early adulthood is sufficient to promote healthy longevity. Mechanistically, these beneficial effects upon pitp-1 reduction are mediated by suppressing TOR signaling. Conversely, pitp-1 overexpression shortens lifespan and impairs healthspan via TOR activation. Moreover, pitp-1 is transcriptionally repressed by DAF-16 downstream of insulin/IGF-1 signaling (IIS), and contributes to IIS-mediated lifespan extension. <h4>Conclusion</h4> These findings identify pitp-1 as a novel regulator of healthy aging that integrates IIS and TOR pathways, providing new insights into conserved mechanisms for promoting healthy longevity.

◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:

Read at source →

Provenance

Source
Europe PMC
DOI
10.1101/2025.11.28.691094
Canonical
link ↗
Fetched
2026-07-02 MST

Cite this

APA
Y, L., Y, L., S, L., T, L., MM, S., P, H., C, C., T, C., OI, W., C, Y., &amp; H., W. (2025). <i>Phosphatidylinositol Transfer Protein-1</i> Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in <i>Caenorhabditis elegans</i>. https://doi.org/10.1101/2025.11.28.691094
Vancouver
Y L, Y L, S L, T L, MM S, P H, et al. <i>Phosphatidylinositol Transfer Protein-1</i> Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in <i>Caenorhabditis elegans</i>. 2025. doi:10.1101/2025.11.28.691094.
BibTeX
@unpublished{lin2025iPhosp, title = {<i>Phosphatidylinositol Transfer Protein-1</i> Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in <i>Caenorhabditis elegans</i>}, author = {Lin Y and Liao Y and Liao S and Lin T and Shanmugam MM and Hsu P and Chen C and Ching T and Wagner OI and Yuh C and Wang H.}, year = {2025}, doi = {10.1101/2025.11.28.691094}, }

Research neighborhood

References, citing works, and semantically nearest findings. Click a node to open it.