Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Apr 24;104(8):987-94.
doi: 10.1161/CIRCRESAHA.108.189530. Epub 2009 Mar 19.

Endothelium-dependent cerebral artery dilation mediated by TRPA1 and Ca2+-Activated K+ channels

Affiliations

Endothelium-dependent cerebral artery dilation mediated by TRPA1 and Ca2+-Activated K+ channels

Scott Earley et al. Circ Res. .

Abstract

Although it is well established that changes in endothelial intracellular [Ca(2+)] regulate endothelium-dependent vasodilatory pathways, the molecular identities of the ion channels responsible for Ca(2+) influx in these cells are not clearly defined. The sole member of the ankyrin (A) transient receptor potential (TRP) subfamily, TRPA1, is a Ca(2+)-permeable nonselective cation channel activated by electrophilic compounds such as acrolein (tear gas), allicin (garlic), and allyl isothiocyanate (AITC) (mustard oil). The present study examines the hypothesis that Ca(2+) influx via TRPA1 causes endothelium-dependent vasodilation. The effects of TRPA1 activity on vascular tone were examined using isolated, pressurized cerebral arteries. AITC induced concentration-dependent dilation of pressurized vessels with myogenic tone that was accompanied by a corresponding decrease in smooth muscle intracellular [Ca(2+)]. AITC-induced dilation was attenuated by disruption of the endothelium and when the TRPA1 channel blocker HC-030031 was present in the arterial lumen. TRPA1 channels were found to be present in native endothelial cells, localized to endothelial cell membrane projections proximal to vascular smooth muscle cells. AITC-induced dilation was insensitive to nitric oxide synthase or cyclooxygenase inhibition but was blocked by luminal administration of the small and intermediate conductance Ca(2+)-activated K(+) channel blockers apamin and TRAM34. BaCl(2), a blocker of inwardly rectifying K(+) channels, also inhibited AITC-induced dilation. AITC-induced smooth muscle cell hyperpolarization was blocked by apamin and TRAM34. We conclude that Ca(2+) influx via endothelial TRPA1 channels elicits vasodilation of cerebral arteries by a mechanism involving endothelial cell Ca(2+)-activated K(+) channels and inwardly rectifying K(+) channels in arterial myocytes.

PubMed Disclaimer

Figures

Figure 1
Figure 1. The TRPA1 Agonist AITC Elicits Vasodilation of Cerebral Arteries
A: Representative recording of AITC (30 μM)-induced dilation and decrease in vessel wall [Ca2+] of an isolated cerebral artery with myogenic tone (70 mmHg). B: Vasodilation (normalized to passive diameter recorded under Ca2+-free conditions) in response to increasing concentrations of AITC. n=5–11 per concentration. C: Decrease in vessel wall [Ca2+] (expressed as change in 340/380 ratio) in response to increasing concentrations of AITC. n=6–11 per concentration. D: Concentration response data normalized to maximum vasodilation. EC50 = 16.4 μM.
Figure 2
Figure 2. Endothelial Cell TRPA1 Channels Mediate AITC-Induced Vasodilation
A: Vasodilation in response to AITC (100 μM) before and after disruption of endothelial cell function. B: Summary data of the effects of endothelium disruption on AITC-induced vasodilation. n=3. *P≤0.05 vs. Control. C: Vasodilation in response to AITC (100 μM) before and after luminal administration of the TRPA1 blocker HC-030031 (3 μM). D: Summary data for the effects of luminal HC-030031 on AITC-induced vasodilation. n=5. *P≤0.05 vs. Control.
Figure 3
Figure 3. TRPA1 is Present in Endothelial Cells Isolated from Rat Cerebral Arteries
A: RT-PCR for TRPA1 using total RNA from freshly-isolated rat cerebral artery endothelial cells (EC). NT = No template control, −RT = no reverse transcriptase control. Data are representative of RNA isolated from three rats. B–H: Localization of TRPA1 and KCa3.1 channels in cerebral artery endothelial cell membrane projections. Images show immunostaining for TRPA1 (red) (C–E) and KCa3.1 (red) (F–H). The level of the internal elastic lamina (IEL) is shown in green. Black holes (arrow) in the IEL indicate endothelial cell membrane projections in the direction of vascular smooth muscle cells (C and F). Superimposed images demonstrate that TRPA1 channels and KCa3.1 channels are abundant in the holes in the IEL (E, H). Bar = 20 μm. I: Z-stack image showing projection of TRPA1 immunostaining though the IEL. Bar =10 μm. I–L: Co-immunostaining for TRPA1 and KCa3.1 in cerebral artery endothelial cell membrane projections. The level of the internal elastic lamina (IEL) is shown in green (I). Black holes (arrow) in the IEL indicate endothelial cell membrane projections in the direction of vascular smooth muscle cells. J: Immunostaining for TRPA1 (red) K: Immunostaining for KCa3.1 (blue). L: Superimposed images demonstrate that TRPA1 channels and KCa3.1 channels co-localize in black holes in the IEL. Bar = 25 μm. All immunostaing data are representative of arteries isolated from at least three animals.
Figure 4
Figure 4. TRPA1-Dependent Vasodilation Requires KCa and KIR Channels
A: Representative recordings of vasodilation in response to AITC (10 μM) before and after luminal administration of the SKCa blocker apamin (1 μM) and the KCa3.1 blocker TRAM34 (1 μM). B: Summary of the effects of KCa3.1 blockade on AITC-induced dilation. n=5. C: Summary of the effects of SKCa/KCa3.1 blockade on AITC-induced vasodilation. n=5. *P≤0.05 vs. Control. D: Representative recording of vasodilation in response to AITC (10 μM) in the presence of the KIR blocker BaCl2 (30 μM). E: Summary of the effects BaCl2 on AITC-induced vasodilation. n=5. *P≤0.05 vs. Control.
Figure 5
Figure 5. TRPA1 Channel Activation Hyperpolarizes Cerebral Artery Myocytes
AC: Representative membrane potential recordings of smooth muscle cells in pressurized (70 mmHg) cerebral arteries under control conditions (A), in the presence of AITC (30 μM) (B), and in the presence of AITC (30 μM) following luminal administration apamin (1 μM) and TRAM34 (1 μM) (C). D: Summary data for the effects of AITC (30 μM) on smooth muscle cell membrane potential. Data are from tissue isolated from three animals. n= 7 cells for each group. *P≤0.05 vs. Control. E: Summary data for the effects of AITC (30 μM) on smooth muscle cell membrane potential when apamin (1 μM) and TRAM34 (1 μM) was present in the arterial lumen. Data are from tissue isolated from three animals. n=5–7 cells per group. There were no significant differences.
Figure 6
Figure 6. Proposed Signaling Pathway for TRPA1-Mediated Vasodilation of Cerebral Arteries
EC, endothelial cell; VSMC, vascular smooth muscle cell; IEL, internal elastic lamina; MEGJ, myoendothelial gap junction; AITC, Ally isothiocyanate; KCa3.1, intermediate conductance Ca2+-activated K+ channel; KCa2.3, small conductance Ca2+-activated K+ channel; KIR, inwardly rectifying K+ channel.

Similar articles

Cited by

References

    1. Bredt DS, Snyder SH. Isolation of nitric oxide synthetase, a calmodulin-requiring enzyme. Proc Natl Acad Sci U S A. 1990;87:682–685. - PMC - PubMed
    1. Brotherton AF, Hoak JC. Role of Ca2+ and cyclic AMP in the regulation of the production of prostacyclin by the vascular endothelium. Proc Natl Acad Sci U S A. 1982;79:495–499. - PMC - PubMed
    1. Coleman HA, Tare M, Parkington HC. K+ currents underlying the action of endothelium-derived hyperpolarizing factor in guinea-pig, rat and human blood vessels. J Physiol. 2001;531:359–373. - PMC - PubMed
    1. Taylor MS, Bonev AD, Gross TP, Eckman DM, Brayden JE, Bond CT, Adelman JP, Nelson MT. Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure. Circ Res. 2003;93:124–131. - PubMed
    1. Edwards G, Dora KA, Gardener MJ, Garland CJ, Weston AH. K+ is an endothelium-derived hyperpolarizing factor in rat arteries. Nature. 1998;396:269–272. - PubMed

Publication types

MeSH terms