Acute Stressor Exposure Modifies Plasma Exosome-Associated Heat Shock Protein 72 (Hsp72) and microRNA ( miR-142-5p and miR-203)

作者：Beninson, Lida A.; Brown, Peter N.; Loughridge, Alice B.; Saludes, Jonel P.; Maslanik, Thomas; Hills, Abigail K.; Woodworth, Tyler; Craig, Wendy; Yin, Hang; Fleshner, Monika^*

来源：PLos One, 2014, 9(9): e108748.

DOI：10.1371/journal.pone.0108748

• EXTRACELLULAR HSP72
• CELLS
• INDUCTION
• IMMUNITY
• PATHWAY
• HEAT-SHOCK-PROTEIN-70
• ACTIVATION
• RESISTANCE
• MEMBRANE
• ALPHA

Exosomes, biologically active nanoparticles (40-100 nm) released by hematopoietic and non-hematopoietic cells, contain a variety of proteins and small, non-coding RNA known as microRNA (miRNA). Exposure to various pathogens and disease states modifies the composition and function of exosomes, but there are no studies examining in vivo exosomal changes evoked by the acute stress response. The present study reveals that exposing male Fisher 344 rats to an acute stressor modulates the protein and miRNA profile of circulating plasma exosomes, specifically increasing surface heat shock protein 72 (Hsp72) and decreasing miR-142-5p and -203. The selected miRNAs and Hsp72 are associated with immunomodulatory functions and are likely a critical component of stress-evoked modulation of immunity. Further, we demonstrate that some of these stress-induced modifications in plasma exosomes are mediated by sympathetic nervous system (SNS) activation of alpha-1 adrenergic receptors (ADRs), since drug-mediated blockade of the receptors significantly attenuates the stress-induced modifications of exosomal Hsp72 and miR-142-5p. Together, these findings demonstrate that activation of the acute stress response modifies the proteomic and miRNA profile of exosomes released into the circulation.

• 出版日期2014-9-26
• 单位清华大学