Department of Medical Biophysics, Schulich School of Medicine and Dentistry, University of Western Ontario, 1151 Richmond St. N., London, ON N6A 3K7, Canada.
Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON N6A 3K7, Canada.
Int J Mol Sci. 2024 Mar 31;25(7):3913. doi: 10.3390/ijms25073913.
Endothelial autophagy plays an important role in the regulation of endothelial function. The inhibition of endothelial autophagy is associated with the reduced expression of (); however, its role in endothelial cells is not known. Here, we report that endothelial cell-specific loss of PDIA-4 leads to impaired autophagic flux accompanied by loss of endothelial function and apoptosis. Endothelial cell-specific loss of PDIA-4 also induced marked changes in endothelial cell architecture, accompanied by the loss of endothelial markers and the gain of mesenchymal markers consistent with endothelial-to-mesenchymal transition (EndMT). The loss of PDIA-4 activated TGFβ-signaling, and inhibition of TGFβ-signaling suppressed EndMT in -silenced endothelial cells in vitro. Our findings help elucidate the role of PDIA-4 in endothelial autophagy and endothelial function and provide a potential target to modulate endothelial function and/or limit autophagy and EndMT in (patho-)physiological conditions.
内皮细胞自噬在调节内皮功能方面发挥着重要作用。内皮细胞自噬的抑制与 ()的表达减少有关;然而,其在内皮细胞中的作用尚不清楚。在这里,我们报告内皮细胞特异性缺失 PDIA-4 导致自噬通量受损,伴有内皮功能障碍和细胞凋亡。内皮细胞特异性缺失 PDIA-4 也诱导内皮细胞结构的显著变化,伴随着内皮标志物的丢失和间充质标志物的获得,这与内皮-间充质转化(EndMT)一致。PDIA-4 的缺失激活了 TGFβ 信号通路,并且 TGFβ 信号通路的抑制抑制了体外沉默 PDIA-4 的内皮细胞中的 EndMT。我们的发现有助于阐明 PDIA-4 在内皮细胞自噬和内皮功能中的作用,并为调节内皮功能和/或在(病理)生理条件下限制自噬和 EndMT 提供了一个潜在的靶点。