Stable Flow-induced Expression of KLK10 Inhibits Endothelial Inflammation and Atherosclerosis

Williams, D.; Mahmoud, M.; Liu, R.; Andueza, A.; Kumar, S.; Kang, D.-W.; Zhang, J.; Tamargo, I.; Villa-Roel, N.; Baek, K.-I.; Lee, H.; An, Y.; Zhang, L.; Tate, E. W.; Bagchi, P.; Pohl, J.; Mosnier, L.; Diamandis, E. P.; Mihara, K.; Hollenberg, M.; Dai, Z.; Jo, H.

doi:10.1101/2021.08.10.455857

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bioRxiv · 10.1101/2021.08.10.455857

Stable Flow-induced Expression of KLK10 Inhibits Endothelial Inflammation and Atherosclerosis

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Abstract

IntroductionAtherosclerosis preferentially occurs in arterial regions exposed to disturbed blood flow (d-flow), while regions exposed to stable flow (s-flow) are protected. The proatherogenic and atheroprotective effects of d-flow and s-flow are mediated in part by the global changes in endothelial cell gene expression, which regulates endothelial dysfunction, inflammation, and atherosclerosis. Previously, we identified Kallikrein-Related Peptidase 10 (KLK10, a secreted serine protease) as a flow-sensitive gene in arterial endothelial cells, but its role in endothelial biology and atherosclerosis was unknown. Methods and ResultsHere, we show that KLK10 is upregulated under s-flow conditions and downregulated under d-flow conditions using in vivo mouse models and in vitro studies with cultured endothelial cells (ECs). Single-cell RNA sequencing (scRNAseq) and scATAC sequencing (scATACseq) study using the partial carotid ligation mouse model showed flow-regulated KLK10 expression at the epigenomic and transcription levels. Functionally, KLK10 protected against d-flow-induced inflammation and permeability dysfunction in human artery ECs (HAECs). Further, treatment of mice in vivo with rKLK10 decreased arterial endothelial inflammation in d-flow regions. Additionally, rKLK10 injection or ultrasound-mediated transfection of KLK10-expressing plasmids inhibited atherosclerosis in ApoE-/- mice. Studies using pharmacological inhibitors and siRNAs revealed that the anti-inflammatory effects of KLK10 were mediated by a Protease Activated Receptors (PAR1/2)-dependent manner. However, unexpectedly, KLK10 did not cleave the PARs. Through a proteomics study, we identified HTRA1 (High-temperature requirement A serine peptidase 1), which bound and cleaved KLK10. Further, siRNA knockdown of HTRA1 prevented KLK10s anti-inflammatory and barrier protective function in HAECs, suggesting that HTRA1 regulates KLK10 function. Moreover, KLK10 expression was significantly reduced in human coronary arteries with advanced atherosclerotic plaques compared to those with less severe plaques. ConclusionKLK10 is a flow-sensitive endothelial protein and, in collaboration with HTRA1, serves as an anti-inflammatory, barrier-protective, and anti-atherogenic factor.

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Williams, D., Mahmoud, M., Liu, R., Andueza, A., Kumar, S., Kang, D.-W., Zhang, J., Tamargo, I., Villa-Roel, N., Baek, K.-I., Lee, H., An, Y., Zhang, L., Tate, E. W., Bagchi, P., Pohl, J., Mosnier, L., Diamandis, E. P., Mihara, K., Hollenberg, M., Dai, Z., Jo, H.. 2021-08-10. Stable Flow-induced Expression of KLK10 Inhibits Endothelial Inflammation and Atherosclerosis. https://doi.org/10.1101/2021.08.10.455857

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