Abstract

Living cells obtain energy either by oxidizing reduced compounds of organic or mineral origin or by absorbing light. Whichever energy source is used, some of the energy released is conserved by converting adenosine diphosphate (ADP) to adenosine triphosphate (ATP), which are analogous to the chemicals in a rechargeable battery. The energy released by the conversion of ATP back to ADP is used to drive most energy-requiring processes, including cell growth, cell division, communication and movement. It is clearly essential to life that the production and consumption of ATP are always maintained in balance, and the AMP-activated protein kinase (AMPK) is one of the key cellular regulatory systems that ensures this. In eukaryotic cells (cells with nuclei and other internal membrane-bound structures, including human cells), most ATP is produced in mitochondria, which are thought to have been derived by the engulfment of oxidative bacteria by a host cell not previously able to use molecular oxygen. AMPK is activated by increasing AMP or ADP (AMP being generated from ADP whenever ADP rises) coupled with falling ATP. Relatives of AMPK are found in essentially all eukaryotes, and it may have evolved to allow the host cell to monitor the output of the newly acquired mitochondria and step their ATP production up or down according to the demand. Structural studies have illuminated how AMPK achieves the task of detecting small changes in AMP and ADP, despite the presence of much higher concentrations of ATP. Recently, it has been shown that AMPK can also sense the availability of glucose, the primary carbon source for most eukaryotic cells, via a mechanism independent of changes in AMP or ADP. Once activated by energy imbalance or glucose lack, AMPK modifies many target proteins by transferring phosphate groups to them from ATP. By this means, numerous ATP-producing processes are switched on (including the production of new mitochondria) and ATP-consuming processes are switched off, thus restoring energy homeostasis. Drugs that modulate AMPK have great potential in the treatment of metabolic disorders such as obesity and Type 2 diabetes, and even cancer. Indeed, some existing drugs such as metformin and aspirin, which were derived from traditional herbal remedies, appear to work, in part, by activating AMPK.

Highlights

  • Division of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, UK

  • AMPK is expressed universally in all eukaryotes, with the notable exception of certain parasites that mainly reproduce inside other eukaryotic cells, which may have been able to dispense with AMPK, because their host cell would provide it

  • The classical or canonical role of the AMPK system is a sensor of cellular energy status, and we speculate that it may have evolved quite soon after the endosymbiotic acquisition of aerobic bacteria into an archaeal host cell, which many people believe is the critical event that led to the development of the first eukaryote

Read more

Summary

Grahame Hardie

Division of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, UK. Relatives of AMPK are found in essentially all eukaryotes, and it may have evolved to allow the host cell to monitor the output of the newly acquired mitochondria and step their ATP production up or down according to the demand. It has been shown that AMPK can sense the availability of glucose, the primary carbon source for most eukaryotic cells, via a mechanism independent of changes in AMP or ADP. Once activated by energy imbalance or glucose lack, AMPK modifies many target proteins by transferring phosphate groups to them from ATP. By this means, numerous ATP-producing processes are switched on (including the production of new mitochondria) and ATP-consuming processes are switched off, restoring energy homeostasis. Some existing drugs such as metformin and aspirin, which were derived from traditional herbal remedies, appear to work, in part, by activating AMPK

Being alive requires a constant and rechargeable source of energy
Protein kinases and phosphatases act as molecular switches
AMPK is expressed in almost all eukaryotes
Eukaryotes that lack AMPK: intracellular parasites
Multiple forms of AMPK arose by whole genome duplication
Mechanism of energy-sensing by AMPK
Structure of the AMPK heterotrimer
Conformational changes upon AMP binding to AMPK
The CaMKK2 pathway and effects of hormones on AMPK
Glucose-sensing may be an ancient role of the AMPK system
Mechanism of glucose-sensing by AMPK
What is being sensed and what is the sensor?
Interplay between the AMPK and targetof-rapamycin pathways
Recognition of downstream targets by AMPK
AMPK activation causes a metabolic switch from anabolism to catabolism
Non-metabolic targets of AMPK
Uses of AMPK activators and inhibitors to treat human disease
Conclusion
Kunji ER et al 2016 The transport mechanism of the
45. Xiao B et al 2011 Structure of mammalian AMPK
48. Hawley SA et al 2012 The ancient drug salicylate
Findings
70. Hawley SA et al 2010 Use of cells expressing
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.