Decoding Angiotensin Receptors: TOMAHAQ-Based Detection and Quantification of Angiotensin Type-1 and Type-2 Receptors.
TOMAHAQ (triggered by offset
accurate mass
and absolute quantification)
angiotensin
angiotensin type‐1 receptor
angiotensin type‐2 receptor
brain
high resolution
multiplexed
Journal
Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524
Informations de publication
Date de publication:
19 09 2023
19 09 2023
Historique:
medline:
20
9
2023
pubmed:
8
9
2023
entrez:
8
9
2023
Statut:
ppublish
Résumé
Background The renin-angiotensin system plays a crucial role in human physiology, and its main hormone, angiotensin, activates 2 G-protein-coupled receptors, the angiotensin type-1 and type-2 receptors, in almost every organ. However, controversy exists about the location, distribution, and expression levels of these receptors. Concerns have been raised over the low sensitivity, low specificity, and large variability between lots of commercially available antibodies for angiotensin type-1 and type-2 receptors, which makes it difficult to reconciliate results of different studies. Here, we describe the first non-antibody-based sensitive and specific targeted quantitative mass spectrometry assay for angiotensin receptors. Methods and Results Using a technique that allows targeted analysis of multiple peptides across multiple samples in a single mass spectrometry analysis, known as TOMAHAQ (triggered by offset, multiplexed, accurate mass, high resolution, and absolute quantification), we have identified and validated specific human tryptic peptides that permit identification and quantification of angiotensin type-1 and type-2 receptors in biological samples. Several peptide sequences are conserved in rodents, making these mass spectrometry assays amenable to both preclinical and clinical studies. We have used this method to quantify angiotensin type-1 and type-2 receptors in postmortem frontal cortex samples of older adults (n=28) with Alzheimer dementia. We correlated levels of angiotensin receptors to biomarkers classically linked to renin-angiotensin system activation, including oxidative stress, inflammation, amyloid-β load, and paired helical filament-tau tangle burden. Conclusions These robust high-throughput assays will not only catalyze novel mechanistic studies in the angiotensin research field but may also help to identify patients with an unbalanced angiotensin receptor distribution who would benefit from angiotensin receptor blocker treatment.
Identifiants
pubmed: 37681524
doi: 10.1161/JAHA.123.030791
pmc: PMC10547273
doi:
Substances chimiques
Angiotensins
0
Receptors, Angiotensin
0
Angiotensin Receptor Antagonists
0
Antibodies
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e030791Subventions
Organisme : NIA NIH HHS
ID : P30 AG021334
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG046441
Pays : United States
Organisme : NIA NIH HHS
ID : K23 AG035005
Pays : United States
Références
Front Aging. 2023 Jan 23;4:1117502
pubmed: 36756193
Cell Mol Neurobiol. 2012 Nov;32(8):1353-65
pubmed: 22843099
Proc Natl Acad Sci U S A. 2011 Sep 6;108(36):14849-54
pubmed: 21852574
Anal Chem. 2012 Sep 4;84(17):7469-78
pubmed: 22880955
Front Neurosci. 2020 Sep 30;14:586314
pubmed: 33117127
Pharmacol Rev. 2000 Sep;52(3):415-72
pubmed: 10977869
Rejuvenation Res. 2010 Apr-Jun;13(2-3):195-201
pubmed: 20370487
Geroscience. 2023 Feb;45(1):371-384
pubmed: 35969296
Nature. 2017 Apr 20;544(7650):327-332
pubmed: 28379944
Int J Mol Sci. 2020 Dec 16;21(24):
pubmed: 33339432
J Gerontol A Biol Sci Med Sci. 2021 Jan 18;76(2):211-215
pubmed: 32585682
J Gerontol A Biol Sci Med Sci. 2022 Dec 29;77(12):2356-2366
pubmed: 35511890
J Alzheimers Dis. 2018;62(3):1319-1335
pubmed: 29562533
J Leukoc Biol. 2002 Aug;72(2):233-8
pubmed: 12149413
J Gerontol A Biol Sci Med Sci. 2022 Apr 1;77(4):664-672
pubmed: 34914835
Hypertension. 2013 Apr;61(4):e32
pubmed: 23607135
Front Pharmacol. 2020 Aug 03;11:1179
pubmed: 32848782
Mol Cell. 2017 Jan 19;65(2):361-370
pubmed: 28065596
Am J Physiol Heart Circ Physiol. 2019 Jun 1;316(6):H1426-H1438
pubmed: 30978131
Cell. 2009 Aug 21;138(4):795-806
pubmed: 19664813
Clin Res Cardiol. 2008 Jul;97(7):418-31
pubmed: 18454336
PLoS One. 2013 Jul 01;8(7):e69234
pubmed: 23840911
J Neuroinflammation. 2019 Dec 10;16(1):261
pubmed: 31822279
Nat Med. 2018 Sep;24(9):1418-1429
pubmed: 30038218
Circ Res. 2005 Oct 14;97(8):772-80
pubmed: 16151022
Anal Chem. 2015 Nov 3;87(21):10830-8
pubmed: 26451657
Cell Death Dis. 2016 Oct 20;7(10):e2427
pubmed: 27763643
Nature. 2000 Sep 7;407(6800):94-8
pubmed: 10993080
Brain Res. 1971 Oct 29;33(2):557-9
pubmed: 4332505
Curr Alzheimer Res. 2012 Jul;9(6):646-63
pubmed: 22471867
Mol Neurobiol. 2019 Nov;56(11):7408-7419
pubmed: 31037647
Endocrine. 2011 Jun;39(3):242-50
pubmed: 21484513
Nat Commun. 2015 Jan 12;6:5924
pubmed: 25581283
Clin Geriatr Med. 2011 Feb;27(1):53-65
pubmed: 21093722
Proc Natl Acad Sci U S A. 2012 Sep 18;109(38):15395-400
pubmed: 22949669
J Neuroinflammation. 2020 Aug 17;17(1):243
pubmed: 32807174
Peptides. 2012 Dec;38(2):437-45
pubmed: 23032352
Front Physiol. 2014 Nov 24;5:439
pubmed: 25505418
Pharmacol Rev. 2011 Dec;63(4):901-37
pubmed: 21969326
Int J Mol Sci. 2018 Mar 15;19(3):
pubmed: 29543776
Nat Med. 2001 Sep;7(9):1003-9
pubmed: 11533702
Mol Cell Proteomics. 2012 Nov;11(11):1475-88
pubmed: 22865924
Pharmacol Rev. 2022 Oct;74(4):1051-1135
pubmed: 36180112
Proteomics. 2020 Jun;20(11):e1900105
pubmed: 32032464
Brain Res. 2019 Sep 1;1718:46-52
pubmed: 31054884
Brain Behav Immun. 2020 Jul;87:256-271
pubmed: 31863823
Proteomics. 2005 Nov;5(17):4510-24
pubmed: 16222721