scholarly journals Bone Morphogenetic Protein-2/-4 Upregulation Promoted by Endothelial Cells in Coculture Enhances Mouse Embryoid Body Differentiation

2013 ◽  
Vol 22 (24) ◽  
pp. 3252-3260 ◽  
Author(s):  
Dodanim Talavera-Adame ◽  
Ankur Gupta ◽  
Silvia Kurtovic ◽  
Kira L. Chaiboonma ◽  
Vaithilingaraja Arumugaswami ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Bone Morphogenetic Protein ◽  
Embryoid Body ◽  
Bone Morphogenetic Protein 2 ◽  
Morphogenetic Protein ◽  
Embryoid Body Differentiation

scholarly journals Bone Morphogenetic Protein-2 Induces Non-Canonical Inflammatory and Oxidative Pathways in Human Retinal Endothelial Cells

2021 ◽  
Vol 11 ◽  
Author(s):  
Mohamed Al-Shabrawey ◽  
Khaled Hussein ◽  
Fang Wang ◽  
Ming Wan ◽  
Khaled Elmasry ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Endothelial Cell ◽  
Bone Morphogenetic Protein ◽  
P38 Mapk ◽  
High Glucose ◽  
Bone Morphogenetic Protein 2 ◽  
Barrier Dysfunction ◽  
Retinal Endothelial Cells ◽  
Bmp Receptors ◽  
Morphogenetic Protein

The mechanisms of diabetic retinopathy (DR), are not yet fully understood. We previously demonstrated an upregulation of retinal bone morphogenetic protein-2 (BMP2) in experimental diabetes and in retinas of diabetic human subjects. The purpose of current study was to investigate the role of non-canonical inflammatory pathway in BMP2-induced retinal endothelial cell (REC) barrier dysfunction. For this purpose, we used RT-PCR and western blotting to evaluate the levels of BMP2 signaling components (BMP2, BMP4, BMP receptors), VEGF, phosphorylated p38 MAPK and NFκB, and oxidative stress markers in cultured human retinal endothelial cells (HRECs) subjected to BMP2 (50ng/ml) for up to 24 h. Also, effect of high glucose (HG, 30mM D-glucose) on the expression of BMP2 and its downstream genes was examined in HRECs. H2-DCF is a fluorogenic dye that measures the levels of cellular reactive oxygen species (ROS) was used to measure the pro-oxidative effect of BMP2. Moreover, we evaluated the effect of inhibiting p38 and VEGF signaling on BMP2-induced HRECs barrier dysfunction by measuring the trans-endothelial cell electrical resistance (TER) using electric cell-substrate impedance sensing (ECIS). We also tested the effect of HG on the integrity of HRECs barrier in the presence or absence of inhibitors of BMP2 signaling. Our data reveals that BMP2 and high glucose upregulates BMP components of the BMP signaling pathway (SMAD effectors, BMP receptors, and TGFβ ligand itself) and induces phosphorylation of p38 MAPK and NFκB with nuclear translocation of NFκB. Inhibition of p38 or NFκB attenuated BMP2-induced VEGF expression and barrier dysfunction in HRECs. Also, inhibition of VEGFR2 attenuated BMP2-induced barrier dysfunction. Moreover, BMP2 induces generation of ROS and endothelial nitric oxide synthase (eNOS) expression and activity in HRECs. Finally, HG upregulated BMP2 and its downstream genes (SMAD, BMP4, ALKs, and TGF-β) in HRECs and BMP2 inhibitors attenuated HG-induced HRECs barrier dysfunction. Our results suggest that in addition to the regular canonical SMAD signaling BMP2 induces non-canonical inflammatory pathway in HRECs via activation of p38/NFκB pathway that causes the upregulation of VEGF and the disruption of HRECs. Inhibition of BMP2 signaling is a potential therapeutic intervention to preserve endothelial cell barrier function in DR.

scholarly journals Regulation of Bone Morphogenetic Protein-2 Expression in Endothelial Cells

Circulation ◽  
2005 ◽  
Vol 111 (18) ◽  
pp. 2364-2372 ◽  
Author(s):  
Anna Csiszar ◽  
Kira E. Smith ◽  
Akos Koller ◽  
Gabor Kaley ◽  
John G. Edwards ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Bone Morphogenetic Protein ◽  
Bone Morphogenetic Protein 2 ◽  
Morphogenetic Protein
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