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An uncoupling protein (UCP) is a mitochondrial inner membrane protein that is a regulated proton channel or transporter. An uncoupling protein is thus capable of dissipating the proton gradient generated by NADH-powered pumping of protons from the mitochondrial matrix to the mitochondrial intermembrane space. The energy lost in dissipating the proton gradient via UCPs is not used to do biochemical work. Instead, heat is generated. This is what links UCP to thermogenesis. UCPs are positioned in the same membrane as the ATP synthase, which is also a proton channel. The two proteins thus work in parallel with one generating heat and the other generating ATP from ADP and inorganic phosphate, the last step in oxidative phosphorylation. Mitochondria respiration is coupled to ATP synthesis (ADP phosphorylation) but is regulated by UCPs.

Uncoupling proteins play a role in normal physiology, as in cold exposure or hibernation, because the energy is used to generate heat (see thermogenesis) instead of producing ATP. Some plants species use the heat generated by uncoupling proteins for special purposes. Skunk cabbage, for example, keeps the temperature of its spikes as much as 20° higher than the environment, spreading odor and attracting insects that fertilize the flowers. However, other substances, such as 2,4-dinitrophenol and carbonyl cyanide m-chlorophenyl hydrazone, also serve the same uncoupling function. Salicylic acid is also an uncoupling agent (chiefly in plants) and will decrease production of ATP and increase body temperature if taken in extreme excess. Uncoupling proteins are increased by thyroid hormone, norepinephrine, epinephrine, and leptin.

History

Scientists observed the thermogenic activity in brown adipose tissue, which eventually led to the discovery of UCP₁, initially known as "Uncoupling Protein". The brown tissue revealed elevated levels of mitochondria respiration and another respiration not coupled to ATP synthesis, which symbolized strong thermogenic activity. UCP₁ was the protein discovered responsible for activating a proton pathway that was not coupled to ADP phosphorylation (ordinarily done through ATP Synthase).

In mammals

There are five UCP homologs known in mammals. While each of these performs unique functions, certain functions are performed by several of the homologs. The homologs are as follows:

• UCP1, also known as thermogenin
• UCP2
• UCP3
• SLC25A27, also known as "UCP4"
• SLC25A14, also known as "UCP5"

Maintaining body temperature

The first uncoupling protein discovered, UCP₁, was discovered in the brown adipose tissues of hibernators and small rodents, which provide non-shivering heat to these animals. These brown adipose tissues are essential to maintaining the body temperature of small rodents, and studies with (UCP₁)-knockout mice show that these tissues do not function correctly without functioning uncoupling proteins. In fact, these studies revealed that cold-acclimation is not possible for these knockout mice, indicating that UCP₁ is an essential driver of heat production in these brown adipose tissues.

Elsewhere in the body, uncoupling protein activities are known to affect the temperature in micro-environments. This is believed to affect other proteins' activity in these regions, though work is still required to determine the true consequences of uncoupling-induced temperature gradients within cells.

Role in ATP concentrations

The effect of UCP₂ and UCP₃ on ATP concentrations varies depending on cell type. For example, pancreatic beta cells experience a decrease in ATP concentration with increased activity of UCP_2. This is associated with cell degeneration, decreased insulin secretion, and type II diabetes. Conversely, UCP₂ in hippocampus cells and UCP₃ in muscle cells stimulate production of mitochondria. The larger number of mitochondria increases the combined concentration of ADP and ATP, actually resulting in a net increase in ATP concentration when these uncoupling proteins become coupled (i.e. the mechanism to allow proton leaking is inhibited).

Maintaining concentration of reactive oxygen species

The entire list of functions of UCP₂ and UCP₃ is not known. However, studies indicate that these proteins are involved in a negative-feedback loop limiting the concentration of reactive oxygen species (ROS). Current scientific consensus states that UCP₂ and UCP₃ perform proton transportation only when activation species are present. Among these activators are fatty acids, ROS, and certain ROS byproducts that are also reactive. Therefore, higher levels of ROS directly and indirectly cause increased activity of UCP₂ and UCP₃. This, in turn, increases proton leak from the mitochondria, lowering the proton-motive force across mitochondrial membranes, activating the electron transport chain. therefore, limiting ROS production. This theory is supported by independent studies which show increased ROS production in both UCP₂ and UCP₃ knockout mice.

This process is important to human health, as high-concentrations of ROS are believed to be involved in the development of degenerative diseases.

Functions in neurons

By detecting the associated mRNA, UCP₂, UCP₄, and UCP₅ were shown to reside in neurons throughout the human central nervous system. These proteins play key roles in neuronal function. While many study findings remain controversial, several findings are widely accepted.

For example, UCP's alter the free calcium concentrations in the neuron. Mitochondria are a major site of calcium storage in neurons, and the storage capacity increases with potential across mitochondrial membranes. Therefore, when the uncoupling proteins reduce potential across these membranes, calcium ions are released to the surrounding environment in the neuron. Due to the high concentrations of mitochondria near axon terminals, this implies UCP's play a role in regulating calcium concentrations in this region. Considering calcium ions play a large role neurotransmission, scientists predict that these UCP's directly affect neurotransmission.

As discussed above, neurons in the hippocampus experience increased concentrations of ATP in the presence of these uncoupling proteins. This leads scientists to hypothesize that UCP's improve synaptic plasticity and transmission.

References

1. Nedergaard J, Ricquier D, Kozak LP (2005). "Uncoupling proteins: current status and therapeutic prospects". EMBO Rep. 6 (10): 917–21. doi:10.1038/sj.embor.7400532. PMC 1369193. PMID 16179945.
2. ^ Rousset, Sophie; Alves-Guerra, Marie-Clotilde; Mozo, Julien; Miroux, Bruno; Cassard-Doulcier, Anne-Marie; Bouillaud, Frédéric; Ricquier, Daniel (2004-02-01). "The Biology of Mitochondrial Uncoupling Proteins". Diabetes. 53 (suppl 1): S130 – S135. doi:10.2337/diabetes.53.2007.S130. ISSN 0012-1797. PMID 14749278.
3. Garrett, Reginald H.; Grisham, Charles M. (2013). Biochemistry (Fifth Edition, International ed.). China: Mary Finch. p. 668. ISBN 978-1-133-10879-5.
4. "California Poison Control System: Salicylates". Archived from the original on 2014-08-02. {{cite web}}: Unknown parameter |deadurl= ignored (|url-status= suggested) (help)
5. Gong DW, He Y, Karas M, Reitman M (1997). "Uncoupling protein-3 is a mediator of thermogenesis regulated by thyroid hormone, β3-adrenergic agonists, and leptin". J Biol Chem. 272 (39): 24129–32. doi:10.1074/jbc.272.39.24129. PMID 9305858.{{cite journal}}: CS1 maint: unflagged free DOI (link)
6. ^ Ricquier, Daniel; Bouillaud, Frédéric; Cassard-Doulcier, Anne-Marie; Miroux, Bruno; Mozo, Julien; Alves-Guerra, Marie-Clotilde; Rousset, Sophie (2004-02-01). "The Biology of Mitochondrial Uncoupling Proteins". Diabetes. 53 (suppl 1): S130 – S135. doi:10.2337/diabetes.53.2007.S130. ISSN 1939-327X. PMID 14749278.
7. Hagen, T.; Vidal-Puig, A. (2002-2). "Mitochondrial uncoupling proteins in human physiology and disease". Minerva Medica. 93 (1): 41–57. ISSN 0026-4806. PMID 11850613. {{cite journal}}: Check date values in: |date= (help)
8. Feldmann, Helena M.; Golozoubova, Valeria; Cannon, Barbara; Nedergaard, Jan (2009-2). "UCP1 ablation induces obesity and abolishes diet-induced thermogenesis in mice exempt from thermal stress by living at thermoneutrality". Cell Metabolism. 9 (2): 203–209. doi:10.1016/j.cmet.2008.12.014. ISSN 1932-7420. PMID 19187776. {{cite journal}}: Check date values in: |date= (help)
9. ^ Horvath, Tamas L.; Diano, Sabrina; Andrews, Zane B. (2005-11). "Mitochondrial uncoupling proteins in the cns: in support of function and survival". Nature Reviews Neuroscience. 6 (11): 829–840. doi:10.1038/nrn1767. ISSN 1471-0048. {{cite journal}}: Check date values in: |date= (help)
10. Horvath, T. L.; Warden, C. H.; Hajos, M.; Lombardi, A.; Goglia, F.; Diano, S. (1999-12-01). "Brain uncoupling protein 2: uncoupled neuronal mitochondria predict thermal synapses in homeostatic centers". The Journal of Neuroscience: The Official Journal of the Society for Neuroscience. 19 (23): 10417–10427. ISSN 0270-6474. PMID 10575039.
11. Zhang, Chen-Yu; Baffy, György; Perret, Pascale; Krauss, Stefan; Peroni, Odile; Grujic, Danica; Hagen, Thilo; Vidal-Puig, Antonio J.; Boss, Olivier (2001-06). "Uncoupling Protein-2 Negatively Regulates Insulin Secretion and Is a Major Link between Obesity, β Cell Dysfunction, and Type 2 Diabetes". Cell. 105 (6): 745–755. doi:10.1016/s0092-8674(01)00378-6. ISSN 0092-8674. {{cite journal}}: Check date values in: |date= (help)
12. ^ Horvath, Tamas L.; Barnstable, Colin J.; Beal, M. Flint; Yang, Lichuan; Patrylo, Peter; Matthews, Russell T.; Diano, Sabrina (2003-11-01). "Uncoupling Protein 2 Prevents Neuronal Death Including that Occurring during Seizures: A Mechanism for Preconditioning". Endocrinology. 144 (11): 5014–5021. doi:10.1210/en.2003-0667. ISSN 0013-7227.
13. ^ Brand, Martin D.; Treberg, Jason R.; Mookerjee, Shona; Divakaruni, Ajit S.; Jastroch, Martin (2010-06-14). "Mitochondrial proton and electron leaks". Essays In Biochemistry. 47: 53–67. doi:10.1042/bse0470053. ISSN 1744-1358. PMC 3122475. PMID 20533900.{{cite journal}}: CS1 maint: PMC format (link)
14. ^ "Uncoupling proteins and the control of mitochondrial reactive oxygen species production". Free Radical Biology and Medicine. 51 (6): 1106–1115. 2011-09-15. doi:10.1016/j.freeradbiomed.2011.06.022. ISSN 0891-5849.
15. ^ Brand, Martin D.; Esteves, Telma C. (2005-08). "Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3". Cell Metabolism. 2 (2): 85–93. doi:10.1016/j.cmet.2005.06.002. ISSN 1550-4131. {{cite journal}}: Check date values in: |date= (help)
16. ^ Brand, Martin D.; Esteves, Telma C. (2005-08). "Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3". Cell Metabolism. 2 (2): 85–93. doi:10.1016/j.cmet.2005.06.002. ISSN 1550-4131. {{cite journal}}: Check date values in: |date= (help)
17. Ricquier, D.; Sanchis, D.; Huang, Q.; Clavel, S.; Richard, D. (2001-11-01). "Uncoupling protein 2 in the brain: distribution and function". Biochemical Society Transactions. 29 (6): 812–817. doi:10.1042/bst0290812. ISSN 1470-8752. PMID 11709080.
18. Nicholls, David G.; Ward, Manus W. (2000-04). "Mitochondrial membrane potential and neuronal glutamate excitotoxicity: mortality and millivolts". Trends in Neurosciences. 23 (4): 166–174. doi:10.1016/s0166-2236(99)01534-9. ISSN 0166-2236. {{cite journal}}: Check date values in: |date= (help)

External links

• Uncoupling+Agents at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

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