Key result
Endothelial PDK4 worsens thoracic aortic dissection via pathological EndoMT activation in mice.
Why the study?
The role of endothelial-to-mesenchymal transition (EndoMT) and the functional contribution of PDK4 in thoracic aortic dissection (TAD) remain poorly defined.
Does PDK4 modulation mitigate the development of thoracic aortic dissection in preclinical models?
Does PDK4 modulation mitigate the development of thoracic aortic dissection in preclinical models?
PDK4 drives endothelial-to-mesenchymal transition via lactate accumulation, and its inhibition with dichloroacetate attenuates thoracic aortic dissection progression in mice, highlighting a potential therapeutic target.
BACKGROUND: Thoracic aortic dissection (TAD) is a life-threatening acute vascular condition with high morbidity and mortality. Endothelial cells (ECs) are critical for maintaining vascular homeostasis, yet the role of endothelial-to-mesenchymal transition (EndoMT), a key cell-fate process in vascular development and disease, in TAD remains poorly defined. Furthermore, the functional role of PDK4 (pyruvate dehydrogenase kinase 4) as a driver of this pathological cell-fate transition has not been elucidated. METHODS: To delineate the mechanistic contribution of EndoMT to TAD, we integrated transcriptomic profiling and immunofluorescence analysis in human aortic specimens and a β-aminopropionitrile–induced murine model. Following the identification of PDK4 as a critical downstream effector of EndoMT signaling via RNA-sequencing and chromatin immunoprecipitation assays, its functional role was validated using conditional EC-specific knockout mice and adeno-associated virus–mediated endothelial gene modulation. Serum samples were collected, and ELISA was used to measure levels of endothelial injury markers for assessing EC-dysfunction. In addition, therapeutic potential was assessed using dichloroacetate, a small-molecule PDK4 inhibitor. RESULTS: A robust activation of the EndoMT gene program was observed in both human TAD specimens and murine aortic tissues, characterized by the loss of endothelial identity and acquisition of mesenchymal traits. Transcriptomic screening pinpointed PDK4 as a critical mediator upregulated during EndoMT. Mechanistically, we demonstrated that the transcription factor SNAI1 directly binds to the PDK4 promoter to activate its expression. In turn, excessive PDK4 promotes EndoMT via lactate accumulation, establishing a PDK4-EndoMT positive feedback loop that sustains pathological remodeling in TAD. In vivo, EC-specific Pdk4 overexpression induced spontaneous aortic dissection and rupture. Conversely, EC- Pdk4 -knockdown or pharmacological inhibition with dichloroacetate attenuated TAD progression, preserved vascular integrity, and improved survival. CONCLUSIONS: Our findings demonstrate that the pathological EndoMT program is activated in ECs by PDK4, which aggravates TAD development in β-aminopropionitrile–induced mouse models, highlighting PDK4 as a promising therapeutic target for TAD.
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Cao et al. (2026) studied Thoracic aortic dissection. PDK4 modulation (knockdown or dichloroacetate) was evaluated on Development and progression of thoracic aortic dissection. Endothelial-specific PDK4 knockdown or pharmacological inhibition with dichloroacetate attenuated thoracic aortic dissection progression, preserved vascular integrity, and improved survival in mice.
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