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Mechanoregulation of p38 activity enhances endoplasmic reticulum stress‐mediated inflammation by arterial endothelium
Author(s) -
Bailey Keith A.,
Moreno Emily,
Haj Fawaz G.,
Simon Scott I.,
Passerini Anthony G.
Publication year - 2019
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.201900236r
Subject(s) - xbp1 , endoplasmic reticulum , endothelium , unfolded protein response , microbiology and biotechnology , inflammation , endothelial activation , p38 mitogen activated protein kinases , transcription factor , cell adhesion molecule , chemistry , biology , signal transduction , endocrinology , immunology , biochemistry , mapk/erk pathway , rna , rna splicing , gene
Endothelial up‐regulation of VCAM‐1 at susceptible sites in arteries modulates the recruitment efficiency of inflammatory monocytes that initiates atherosclerotic lesion formation. We reported that hydrodynamic shear stress (SS) mechanoregulates inflammation in human aortic endothelial cells through endoplasmic reticulum (ER) stress via activation of the transcription factor x‐box binding protein 1 (XBP1). Here, a microfluidic flow channel that produces a linear gradient of SS along a continuous monolayer of endothelium was used to delve the mechanisms underlying transcriptional regulation of TNF‐α‐stimulated VCAM‐1 expression. High‐resolution immunofluorescence imaging enabled continuous detection of platelet endothelial cell adhesion molecule 1 (PECAM‐1)‐dependent, outside‐in signaling as a function of SS magnitude. Differential expression of VCAM‐1 and intercellular adhesion molecule 1 (ICAM‐1) was regulated by the spatiotemporal activation of MAPKs, ER stress markers, and transcription factors, which was dependent on the mechanosensing of SS through PECAM‐1 and PI3K. Inhibition of p38 specifically abrogated the rise to peak VCAM‐1 at low SS (2 dyn/cm 2 ), whereas inhibition of ERK1/2 attenuated peak ICAM‐1 at high SS (12 dyn/cm 2 ). A shear stress‐regulated temporal rise in p38 phosphorylation activated the nuclear translocation of XBP1, which together with the transcription factor IFN regulatory factor 1, promoted maximum VCAM‐1 expression. These data reveal a mechanism by which SS sensitizes the endothelium to a cytokine‐induced ER stress response to spatially regulate inflammation promoting atherosclerosis.—Bailey, K. A., Moreno, E., Haj, F. G., Simon, S. I., Passerini, A. G. Mechanoregulation of p38 activity enhances endoplasmic reticulum stress‐mediated inflammation by arterial endothelium. FASEB J. 33, 12888–12899 (2019). www.fasebj.org