Involvement of Rab28 in NF-κB nuclear transport in endothelial cells

• Published in: PloS one 2013-02, Vol.8 (2), p.e56076-e56076
• Main Authors: Jiang, Jun, Qi, Ying-Xin, Zhang, Ping, Gu, Wen-Tian, Yan, Zhi-Qiang, Shen, Bao-Rong, Yao, Qing-Ping, Kong, Han, Chien, Shu, Jiang, Zong-Lai
• Format: Article
• Language: English
• Subjects: Active Transport, Cell Nucleus; Angiotensin; Angiotensin II; Animals; Aorta; Apoptosis; Arteries; Biology; Biotechnology; Blood vessels; Carotid arteries; Carotid artery; Cell Proliferation; Cells, Cultured; Coronary vessels; Cytoplasm; Endothelial cells; Endothelial Cells - cytology; Endothelial Cells - metabolism; Engineering; Gene Expression; Gene Knockdown Techniques; Homeostasis; Hypertension; Immunofluorescence; Immunoprecipitation; Kidneys; Kinases; Life sciences; Mammalian cells; Medicine; Muscle, Smooth, Vascular - cytology; Muscle, Smooth, Vascular - metabolism; Muscles; NF-kappa B - analysis; NF-kappa B - metabolism; NF-κB protein; Nuclear transport; Paracrine signalling; Physiology; rab GTP-Binding Proteins - analysis; rab GTP-Binding Proteins - genetics; rab GTP-Binding Proteins - metabolism; Rats; Rats, Sprague-Dawley; Receptor, Angiotensin, Type 1 - metabolism; Smooth muscle; Translocation; Transport
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0056076

Our previous proteomic analysis revealed the expression of Rab28 in arteries of rats. However, the function of Rab28 in mammalian cells, and its role in vessels are still unknown. Coarctation of abdominal aorta above left kidney artery in rat was used as hypertensive animal model. FX-4000 cyclic strain loading system was used to mimic the mechanical condition on vascular cells during hypertension in vitro. Immunofluorescence and co-immunoprecipitation (Co-IP) were used to identify distribution and interaction of Rab28 and nuclear factor kappa B (NF-κB). Rab28 expression was significantly increased in carotid arteries of hypertensive rats. High cyclic strain induced Rab28 expression of endothelial cells (ECs) through a paracrine control of vascular smooth muscles cells (VSMCs), which at least partly via angiotensin II (Ang II). Rab28 knockdown decreased proliferation of ECs, while increased apoptosis and migration. Immunofluorescence revealed that Ang II stimulated the co-translocation of Rab28 and NF-κB from cytoplasm into nucleus. Knockdown of Rab28 attenuated NF-κB activation. Co-IP of NF-κB p65 and Rab28 indicated their interaction. Our results revealed that Rab28, as a novel regulator of NF-κB nuclear transport, might participate in the disturbance of EC homeostasis.