Parallel Activation of Src and Hif1α Increases Localized Glycolytic ATP Generation for Re-assembly of Endothelial Adherens Junctions

Wang, L.; Gajwani, P.; Chaturvedi, P.; Hong, Z.; Ye, Z.; Schwarz, G.; Pohl-Avila, N.; Ray, A.-M.; Krantz, S.; Toth, P. T.; Leckband, D. E.; Karginov, A. V.; Rehman, J.

doi:10.1101/2022.11.11.516184

bioRxiv · 10.1101/2022.11.11.516184

Parallel Activation of Src and Hif1α Increases Localized Glycolytic ATP Generation for Re-assembly of Endothelial Adherens Junctions

Wang, L.·Gajwani, P.·Chaturvedi, P.·Hong, Z.·Ye, Z.·Schwarz, G.·Pohl-Avila, N.·Ray, A.-M.·Krantz, S.·Toth, P. T.·Leckband, D. E.·Karginov, A. V.·Rehman, J.

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Abstract

Endothelial adherens junctions (AJs) are critical for the regulation of vascular barrier integrity and undergo dis-assembly during inflammatory injury, thus causing vascular leakiness. AJ re-assembly is thus necessary for restoration of the endothelial barrier following the initial injury. Here we examine the metabolic underpinnings that drive restoration of vascular integrity. In response to inflammatory stimuli, the glycolysis regulatory enzyme PFKFB3 is activated, resulting in a rapid and sustained increase of intracellular glycolytic ATP, especially in the proximity of AJs at the plasma membrane. We engineered a novel chemo-genetic construct (RapT) which allowed for precise temporal control of PFKFB3 recruitment to the plasma membrane. Activation of RapT by rapamycin during the barrier restoration phase increased regional ATP and accelerated AJ re-assembly. Mechanistically, we observed that PFKFB3 is activated through two modes. Src-mediated post-translational phosphorylation rapidly increases PFKFB3 activity. Using another chemo-genetic approach to temporally control Src activity, we found that Src activates PFKFB3 by binding to and phosphorylating it at residues Y175, Y334, and Y363. Tyrosine-phospho-deficient mutants of PFKFB3 at these residues block the glycolytic activation upon inflammatory stimuli. In parallel, elevated reactive oxygen species generated during inflammatory stimulation create pockets of regional hypoxia and allow for increased Hif1-mediated transcription of PFKFB3, leading to sustained glycolytic activation. Moreover, inhibition of PFKFB3 delays AJ reassembly and restoration of vascular integrity both in vitro and in vivo. In conclusion, we show that while inflammatory activation acutely compromises the endothelial barrier, inflammatory signaling also concomitantly generates a metabolic milieu in anticipation of the subsequent re-assembly of AJs and restoration of the vascular barrier.

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Wang, L., Gajwani, P., Chaturvedi, P., Hong, Z., Ye, Z., Schwarz, G., Pohl-Avila, N., Ray, A.-M., Krantz, S., Toth, P. T., Leckband, D. E., Karginov, A. V., Rehman, J.. 2022-11-12. Parallel Activation of Src and Hif1α Increases Localized Glycolytic ATP Generation for Re-assembly of Endothelial Adherens Junctions. https://doi.org/10.1101/2022.11.11.516184

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