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Biology subjects

Jiang, O.

Publications and source records attributed to Jiang, O..

2 recordsLinked to original sources

Sialin2 Senses Nitrate to Activate Endosomal PI3K-AKT-NOS Signaling

Nitrate functions as a signaling molecule beyond its metabolic intermediate role. Despite progress in plants, the mechanisms underlying mammalian nitrate sensing and signaling remain unclear. The accompanying study identifies Sialin2--a proteolytic fragment of nitrate transporter Sialin--as a mammalian nitrate sensor mediating cellular responses. Here, we demonstrate that nitrate triggers endocytosis, inducing Sialin proteolysis and Sialin2 generation. Nitrate-induced Sialin2 scaffolds Lyn kinase with epidermal growth factor receptor (EGFR) at endosomes, activating phosphatidylinositol 3-kinase (PI3K)-AKT-nitric oxide synthase (NOS) pathway to stimulate localized nitric oxide (NO) production, enhancing angiogenesis and cell survival. In hypertensive rats, nitrate supplementation restores endothelial function and reduces blood pressure through AKT/eNOS-dependent signaling. Unlike the classical nitrate-nitrite-NO pathway, the Sialin2-PI3K-AKT-NOS axis confines NO synthesis to endosomal microdomains, enabling spatiotemporally precise vasodilation. By establishing Sialin2 as a mammalian nitrate sensor, this study unveils a novel paradigm in nitrogen homeostasis and provides targeted therapeutic strategies for vascular disorders.

cell biology↗

Sialin2 Functions as a Mammalian Nitrate Sensor to Sustain Mitochondrial Homeostasis

Nitrogen homeostasis is fundamental for cellular physiology, yet mammalian nitrate (NO3-) sensing mechanisms remain elusive. Here, we identify Sialin2--a proteolytic fragment of the nitrate transporter Sialin generated by cathepsin B (CTSB) cleavage-- as the first mammalian nitrate sensor. Microscale thermophoresis (MST) reveals Sialin2 as a high-affinity nitrate sensor, while Cryo-Electron Microscopy (Cryo-EM) uncovers its structural basis for signaling. We show that Sialin2 localizes to mitochondria and scaffolds liver kinase B1 (LKB1)-AMP-activated protein kinase (AMPK) complexes to drive organelle-specific metabolic adaptation via spatiotemporally controlled AMPK activation, enhancing mitochondrial biogenesis, ATP production, and cell survival. Real-time tracking using the sCiSiNiS biosensor demonstrates nitrate signaling dynamics at physiological levels. This signaling axis redefines nitrate as a direct ligand activating receptor-like cascades, independent of classical nitric oxide synthesis. Our findings establish a paradigm of "inorganic salt signaling biology", wherein anions co-opt trafficking systems to achieve signaling specificity, offering therapeutic avenues for mitochondrial disorders.

cell biology↗