G protein-coupled receptor systems and their lipid environment in health disorders during aging
- PMID: 17070497
- DOI: 10.1016/j.bbamem.2006.09.024
G protein-coupled receptor systems and their lipid environment in health disorders during aging
Abstract
Cells, tissues and organs undergo phenotypic changes and deteriorate as they age. Cell growth arrest and hyporesponsiveness to extrinsic stimuli are all hallmarks of senescent cells. Most such external stimuli received by a cell are processed by two different cell membrane systems: receptor tyrosine kinases (RTKs) and G protein-coupled receptors (GPCRs). GPCRs form the largest gene family in the human genome and they are involved in most relevant physiological functions. Given the changes observed in the expression and activity of GPCRs during aging, it is possible that these receptors are directly involved in aging and certain age-related pathologies. On the other hand, both GPCRs and G proteins are associated with the plasma membrane and since lipid-protein interactions regulate their activity, they can both be considered to be sensitive to the lipid environment. Changes in membrane lipid composition and structure have been described in aged cells and furthermore, these membrane changes have been associated with alterations in GPCR mediated signaling in some of the main health disorders in elderly subjects. Although senescence could be considered a physiologic process, not all aging humans develop the same health disorders. Here, we review the involvement of GPCRs and their lipid environment in the development of the major human pathologies associated with aging such as cancer, neurodegenerative disorders and cardiovascular pathologies.
Similar articles
-
Lipid-protein interactions in GPCR-associated signaling.Biochim Biophys Acta. 2007 Apr;1768(4):836-52. doi: 10.1016/j.bbamem.2006.09.001. Epub 2006 Sep 16. Biochim Biophys Acta. 2007. PMID: 17067547 Review.
-
Lipid modulation of early G protein-coupled receptor signalling events.Biochim Biophys Acta. 2015 Nov;1848(11 Pt A):2889-97. doi: 10.1016/j.bbamem.2015.08.004. Epub 2015 Aug 11. Biochim Biophys Acta. 2015. PMID: 26275588
-
Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs.Curr Med Chem. 2013;20(1):22-38. Curr Med Chem. 2013. PMID: 23151000 Review.
-
G Protein-Coupled Receptor Systems and Their Role in Cellular Senescence.Comput Struct Biotechnol J. 2019 Aug 23;17:1265-1277. doi: 10.1016/j.csbj.2019.08.005. eCollection 2019. Comput Struct Biotechnol J. 2019. PMID: 31921393 Free PMC article. Review.
-
Crosstalk coregulation mechanisms of G protein-coupled receptors and receptor tyrosine kinases.Methods Mol Biol. 2006;332:51-77. doi: 10.1385/1-59745-048-0:51. Methods Mol Biol. 2006. PMID: 16878685 Review.
Cited by
-
Oleic acid content is responsible for the reduction in blood pressure induced by olive oil.Proc Natl Acad Sci U S A. 2008 Sep 16;105(37):13811-6. doi: 10.1073/pnas.0807500105. Epub 2008 Sep 4. Proc Natl Acad Sci U S A. 2008. PMID: 18772370 Free PMC article.
-
Modulation of the interaction between neurotensin receptor NTS1 and Gq protein by lipid.J Mol Biol. 2012 Mar 16;417(1-2):95-111. doi: 10.1016/j.jmb.2012.01.023. Epub 2012 Jan 27. J Mol Biol. 2012. PMID: 22306739 Free PMC article.
-
Cholesterol modulates the dimer interface of the β₂-adrenergic receptor via cholesterol occupancy sites.Biophys J. 2014 Mar 18;106(6):1290-300. doi: 10.1016/j.bpj.2014.02.002. Biophys J. 2014. PMID: 24655504 Free PMC article.
-
Downregulation of thromboxane A2 and angiotensin II type 1 receptors associated with aging-related decrease in internal anal sphincter tone.Sci Rep. 2019 May 1;9(1):6759. doi: 10.1038/s41598-019-42894-4. Sci Rep. 2019. PMID: 31043680 Free PMC article.
-
Pheromone sensing regulates Caenorhabditis elegans lifespan and stress resistance via the deacetylase SIR-2.1.Proc Natl Acad Sci U S A. 2013 Apr 2;110(14):5522-7. doi: 10.1073/pnas.1214467110. Epub 2013 Mar 18. Proc Natl Acad Sci U S A. 2013. PMID: 23509272 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical