TPM4 condensates glycolytic enzymes and facilitates actin reorganization under hyperosmotic stress

Actin homeostasis is fundamental for cell structure and consumes a large portion of cellular ATP. It has been documented in the literature that certain glycolytic enzymes can interact with actin, indicating an intricate interplay between the cytoskeleton and cellular metabolism. Here we report that hyperosmotic stress triggers actin severing and subsequent phase separation of the actin-binding protein tropomyosin 4 (TPM4). TPM4 condensates recruit glycolytic enzymes such as HK2, PFKM, and PKM2, while wetting actin filaments. Notably, the condensates of TPM4 and glycolytic enzymes are enriched of NADH and ATP, suggestive of their functional importance in cell metabolism. At cellular level, actin filament assembly is enhanced upon hyperosmotic stress and TPM4 condensation, while depletion of TPM4 impairs osmolarity-induced actin reorganization. At tissue level, colocalized condensates of TPM4 and glycolytic enzymes are observed in renal tissues subjected to hyperosmotic stress. Together, our findings suggest that stress-induced actin perturbation may act on TPM4 to organize glycolytic hubs that tether energy production to cytoskeletal reorganization.

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Publication Details

Journal
Cell Discovery
Published
2024-12-03
DOI
https://doi.org/10.1038/s41421-024-00744-2
Citations
13
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
3.04
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article

TPM4 condensates glycolytic enzymes and facilitates actin reorganization under hyperosmotic stress

Congying Wu, Geyao Liu, Yan Wang, Yuan Wang et al.
13 citations
Cell Discovery
RNA Research and Splicing
3.04
article

TPM4 condensates glycolytic enzymes and facilitates actin reorganization under hyperosmotic stress

Congying Wu, Geyao Liu, Yan Wang, Yuan Wang, Wudao Yang
article en
13 citations

Abstract

Actin homeostasis is fundamental for cell structure and consumes a large portion of cellular ATP. It has been documented in the literature that certain glycolytic enzymes can interact with actin, indicating an intricate interplay between the cytoskeleton and cellular metabolism. Here we report that hyperosmotic stress triggers actin severing and subsequent phase separation of the actin-binding protein tropomyosin 4 (TPM4). TPM4 condensates recruit glycolytic enzymes such as HK2, PFKM, and PKM2, while wetting actin filaments. Notably, the condensates of TPM4 and glycolytic enzymes are enriched of NADH and ATP, suggestive of their functional importance in cell metabolism. At cellular level, actin filament assembly is enhanced upon hyperosmotic stress and TPM4 condensation, while depletion of TPM4 impairs osmolarity-induced actin reorganization. At tissue level, colocalized condensates of TPM4 and glycolytic enzymes are observed in renal tissues subjected to hyperosmotic stress. Together, our findings suggest that stress-induced actin perturbation may act on TPM4 to organize glycolytic hubs that tether energy production to cytoskeletal reorganization.

Cell DiscoveryVol. 10(1)
Peking University (CN), Peking University Cancer Hospital (CN), Ministry of Education (SA), Capital Institute of Pediatrics (CN), Peking University International Hospital (CN)
Affordable and clean energy
Openalex Percentile: Top 8%
RNA Research and Splicing
3.04
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