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Phosphatidylinositol Transfer Protein-1 Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in Caenorhabditis elegans
Yen-Hung Lin, Yun-Hsun Liao, Sin-Bo Liao, Tzu‐Yu Lin, Muniesh Muthaiyan Shanmugam, P. J. Hsu, Chang‐Shi Chen, Tsui‐Ting Ching, Oliver Ingvar Wagner, Chiou‐Hwa Yuh, Horng‐Dar Wang
bioRxiv (Cold Spring Harbor Laboratory) · 2025
Abstract
Abstract Background 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. Methods 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. Results 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. Conclusion 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.
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- 10.1101/2025.11.28.691094
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- 2026-10-08 MST
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APA
Lin, Y., Liao, Y., Liao, S., Lin, T., Shanmugam, M.M., Hsu, P.J., Chen, C., Ching, T., Wagner, O.I., Yuh, C., & Wang, H. (2025). Phosphatidylinositol Transfer Protein-1 Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in Caenorhabditis elegans. <em>bioRxiv (Cold Spring Harbor Laboratory)</em>. https://doi.org/10.1101/2025.11.28.691094
Vancouver
Lin Y, Liao Y, Liao S, Lin T, Shanmugam MM, Hsu PJ, et al. Phosphatidylinositol Transfer Protein-1 Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in Caenorhabditis elegans. bioRxiv (Cold Spring Harbor Laboratory). 2025. doi:10.1101/2025.11.28.691094.
BibTeX
@unpublished{yenhung2025Phosph,
title = {Phosphatidylinositol Transfer Protein-1 Integrates Insulin/IGF-1 and TOR Signaling to Negatively Regulate Lifespan and Healthspan in Caenorhabditis elegans},
author = {Yen-Hung Lin and Yun-Hsun Liao and Sin-Bo Liao and Tzu‐Yu Lin and Muniesh Muthaiyan Shanmugam and P. J. Hsu and Chang‐Shi Chen and Tsui‐Ting Ching and Oliver Ingvar Wagner and Chiou‐Hwa Yuh and Horng‐Dar Wang},
journal = {bioRxiv (Cold Spring Harbor Laboratory)},
year = {2025},
doi = {10.1101/2025.11.28.691094},
}
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Phosphatidylinositol transfer protein-1 integrates insulin/IGF-1 and TOR signaling to negatively regulate lifespan and healthspan in Caenorhabditis elegans
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Additional file 6 of Phosphatidylinositol transfer protein-1 integrates insulin/IGF-1 and TOR signaling to negatively regulate lifespan and healthspan in Caenorhabditis elegans
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