-
Something wrong with this record ?
β-Arrestin 2 and ERK1/2 Are Important Mediators Engaged in Close Cooperation between TRPV1 and µ-Opioid Receptors in the Plasma Membrane
B. Melkes, V. Markova, L. Hejnova, J. Novotny
Language English Country Switzerland
Document type Journal Article
Grant support
790217
Grantová Agentura, Univerzita Karlova
1196120
Grantová Agentura, Univerzita Karlova
SVV-260434/2020
Charles University, Faculty of Science
CZ.1.05/4.1.00/16.0347
European Regional Development Fund
CZ.2.16/3.1.00/21515
State Budget of the Czech Republic
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
32610605
DOI
10.3390/ijms21134626
Knihovny.cz E-resources
- MeSH
- Arrestins metabolism MeSH
- beta-Arrestin 2 metabolism physiology MeSH
- beta-Arrestins metabolism MeSH
- Cell Membrane metabolism physiology MeSH
- Phosphorylation MeSH
- HEK293 Cells MeSH
- TRPV Cation Channels metabolism physiology MeSH
- Humans MeSH
- MAP Kinase Signaling System physiology MeSH
- Morphine metabolism MeSH
- Analgesics, Opioid metabolism MeSH
- Receptors, Opioid, mu metabolism physiology MeSH
- Receptors, Opioid metabolism MeSH
- Signal Transduction MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
The interactions between TRPV1 and µ-opioid receptors (MOR) have recently attracted much attention because these two receptors play important roles in pain pathways and can apparently modulate each other's functioning. However, the knowledge about signaling interactions and crosstalk between these two receptors is still limited. In this study, we investigated the mutual interactions between MOR and TRPV1 shortly after their activation in HEK293 cells expressing these two receptors. After activation of one receptor we observed significant changes in the other receptor's lateral mobility and vice versa. However, the changes in receptor movement within the plasma membrane were not connected with activation of the other receptor. We also observed that plasma membrane β-arrestin 2 levels were altered after treatment with agonists of both these receptors. Knockdown of β-arrestin 2 blocked all changes in the lateral mobility of both receptors. Furthermore, we found that β-arrestin 2 can play an important role in modulating the effectiveness of ERK1/2 phosphorylation after activation of MOR in the presence of TRPV1. These data suggest that β-arrestin 2 and ERK1/2 are important mediators between these two receptors and their signaling pathways. Collectively, MOR and TRPV1 can mutually affect each other's behavior and β-arrestin 2 apparently plays a key role in the bidirectional crosstalk between these two receptors in the plasma membrane.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21012443
- 003
- CZ-PrNML
- 005
- 20210507102620.0
- 007
- ta
- 008
- 210420s2020 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms21134626 $2 doi
- 035 __
- $a (PubMed)32610605
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Melkes, Barbora $u Department of Physiology, Faculty of Science, Charles University, 128 00 Prague, Czech Republic
- 245 10
- $a β-Arrestin 2 and ERK1/2 Are Important Mediators Engaged in Close Cooperation between TRPV1 and µ-Opioid Receptors in the Plasma Membrane / $c B. Melkes, V. Markova, L. Hejnova, J. Novotny
- 520 9_
- $a The interactions between TRPV1 and µ-opioid receptors (MOR) have recently attracted much attention because these two receptors play important roles in pain pathways and can apparently modulate each other's functioning. However, the knowledge about signaling interactions and crosstalk between these two receptors is still limited. In this study, we investigated the mutual interactions between MOR and TRPV1 shortly after their activation in HEK293 cells expressing these two receptors. After activation of one receptor we observed significant changes in the other receptor's lateral mobility and vice versa. However, the changes in receptor movement within the plasma membrane were not connected with activation of the other receptor. We also observed that plasma membrane β-arrestin 2 levels were altered after treatment with agonists of both these receptors. Knockdown of β-arrestin 2 blocked all changes in the lateral mobility of both receptors. Furthermore, we found that β-arrestin 2 can play an important role in modulating the effectiveness of ERK1/2 phosphorylation after activation of MOR in the presence of TRPV1. These data suggest that β-arrestin 2 and ERK1/2 are important mediators between these two receptors and their signaling pathways. Collectively, MOR and TRPV1 can mutually affect each other's behavior and β-arrestin 2 apparently plays a key role in the bidirectional crosstalk between these two receptors in the plasma membrane.
- 650 _2
- $a opioidní analgetika $x metabolismus $7 D000701
- 650 _2
- $a arrestiny $x metabolismus $7 D019390
- 650 _2
- $a buněčná membrána $x metabolismus $x fyziologie $7 D002462
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a MAP kinasový signální systém $x fyziologie $7 D020935
- 650 _2
- $a morfin $x metabolismus $7 D009020
- 650 _2
- $a fosforylace $7 D010766
- 650 _2
- $a receptory opiátové $x metabolismus $7 D011957
- 650 _2
- $a receptory opiátové mu $x metabolismus $x fyziologie $7 D017450
- 650 _2
- $a signální transdukce $7 D015398
- 650 _2
- $a kationtové kanály TRPV $x metabolismus $x fyziologie $7 D050916
- 650 _2
- $a beta arrestin 2 $x metabolismus $x fyziologie $7 D000071560
- 650 _2
- $a beta arrestiny $x metabolismus $7 D000071557
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Markova, Vendula $u Department of Physiology, Faculty of Science, Charles University, 128 00 Prague, Czech Republic
- 700 1_
- $a Hejnova, Lucie $u Department of Physiology, Faculty of Science, Charles University, 128 00 Prague, Czech Republic
- 700 1_
- $a Novotny, Jiri $u Department of Physiology, Faculty of Science, Charles University, 128 00 Prague, Czech Republic
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 21, č. 13 (2020)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32610605 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210420 $b ABA008
- 991 __
- $a 20210507102620 $b ABA008
- 999 __
- $a ok $b bmc $g 1650751 $s 1132822
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 21 $c 13 $e 20200629 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a 790217 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a 1196120 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a SVV-260434/2020 $p Charles University, Faculty of Science
- GRA __
- $a CZ.1.05/4.1.00/16.0347 $p European Regional Development Fund
- GRA __
- $a CZ.2.16/3.1.00/21515 $p State Budget of the Czech Republic
- LZP __
- $a Pubmed-20210420