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Extracellular adenosine-induced Rac1 activation in pulmonary endothelium: Molecular mechanisms and barrier-protective role

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

We have previously shown that Gs-coupled adenosine receptors (A2a) are primarily involved in adenosine-induced human pulmonary artery endothelial cell (HPAEC) barrier enhancement. However, the downstream events that mediate the strengthening of the endothelial cell (EC) barrier via adenosine signaling are largely unknown. In the current study, we tested the overall hypothesis that adenosine-induced Rac1 activation and EC barrier enhancement is mediated by Gs-dependent stimulation of cAMP-dependent Epac1-mediated signaling cascades. Adenoviral transduction of HPAEC with constitutively-active (C/A) Rac1 (V12Rac1) significantly increases transendothelial electrical resistance (TER) reflecting an enhancement of the EC barrier. Conversely, expression of an inactive Rac1 mutant (N17Rac1) decreases TER reflecting a compromised EC barrier. The adenosine-induced increase in TER was accompanied by activation of Rac1, decrease in contractility (MLC dephosphorylation), but not Rho inhibition. Conversely, inhibition of Rac1 activity attenuates adenosine-induced increase in TER. We next examined the role of cAMP-activated Epac1 and its putative downstream targets Rac1, Vav2, Rap1, and Tiam1. Depletion of Epac1 attenuated the adenosine-induced Rac1 activation and the increase in TER. Furthermore, silencing of Rac1 specific guanine nucleotide exchange factors (GEFs), Vav2 and Rap1a expression significantly attenuated adenosine-induced increases in TER and activation of Rac1. Depletion of Rap1b only modestly impacted adenosine-induced increases in TER and Tiam1 depletion had no effect on adenosine-induced Rac1 activation and TER. Together these data strongly suggest that Rac1 activity is required for adenosine-induced EC barrier enhancement and that the activation of Rac1 and ability to strengthen the EC barrier depends, at least in part, on cAMP-dependent Epac1/Vav2/Rap1-mediated signaling.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 5736-5746 (11 pages)

Journal (Volume, Issue Number)

Journal of Cellular Physiology (Volume 233, Issue 8)

Publication milestones

  • Accepted/In press - 01/01/2018
  • Published - 08/2018

Publication status

Published - 08/2018

ISSN

0021-9541

Publication IDs

  • Scopus: 85043390623
  • PubMed: 29168172

Publication metrics

Metrics

SciVal
FWCI
0.81
SciVal
Author count
6
SciVal
citations
7
SciVal
Paper percentile
74
Fractional count
2
Fractional count
0.33
Fractional count
4
Fractional count
0.67
Fractional count
2
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
15
Captures
11

Funding Details

This work was supported by the NIH HL101902. AK-K, PhD, was responsible for study design, performing the majority of experiments, analysis, and interpretation of data, design of the figures, and writing of the manuscript's drafts, KMK, PhD, was responsible for adenoviral ECIS experiments, MC-S, PhD, performed experiments with pharmacological inhibitors, SMB, PhD, was involved in the design and troubleshooting of adenoviral experiments and involved in manuscript writing, DJF, PhD, was responsible for generation of adenoviral constructs and involved in manuscript writing, ADV, PhD, was responsible for overall design of the study and writing of the final version of the manuscript.
FundersFunding numbers
NIH
-
NHLBI
P01HL134610, P01HL101902