User:Jesse D. Kirkpatrick/Notebook/Nikki and Jesse Research Proposal

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(Project Description/Abstract)
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Members of the TRP family, specifically TRPM8 and TRPV4, regulate oxidative phosphorylation via uncoupling protein 1 (UCP1). TRPM8 positively regulates UCP1 and TRPV4 negatively regulates it via inhibition of PGC1-alpha. Uncoupling protein 1 is a major source of thermogenesis, and overexpression of this protein has provided hope for treating obesity and other metabolic conditions. However, the thermogenesis potential of this protein may itself be used as a local heating source, if overexpressed to an appropriate extent. We propose seeding bacteria in a cell and overexpressing UCP1 via TRPV4 inhibition and TRPM8 activation. We believe that this will increase heat production in bacteria, which can be used in a variety of applications.
Members of the TRP family, specifically TRPM8 and TRPV4, regulate oxidative phosphorylation via uncoupling protein 1 (UCP1). TRPM8 positively regulates UCP1 and TRPV4 negatively regulates it via inhibition of PGC1-alpha. Uncoupling protein 1 is a major source of thermogenesis, and overexpression of this protein has provided hope for treating obesity and other metabolic conditions. However, the thermogenesis potential of this protein may itself be used as a local heating source, if overexpressed to an appropriate extent. We propose seeding bacteria in a cell and overexpressing UCP1 via TRPV4 inhibition and TRPM8 activation. We believe that this will increase heat production in bacteria, which can be used in a variety of applications.
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==Background Information==
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TRPV4 negatively regulates UCP1[1]
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TRPM8 positively regulates UCP1[2]
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 +
==Project details and methods==
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Insert methods here
 +
 +
==Predicted Outcomes==
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Increased thermogenesis by activation of UCP1
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 +
==Needed Resources==
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Bacteria
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TRPV4 shRNA
==References==
==References==
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Ye et al. TRPV4 Is a Regulator of Adipose Oxidative Metabolism, Inflammation, and Energy Homeostasis.(2012) Cell Press.151(1): 96-110
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[1]Ye et al. TRPV4 Is a Regulator of Adipose Oxidative Metabolism, Inflammation, and Energy Homeostasis.(2012) Cell Press.151(1): 96-110
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Ma et al. Activation of the cold-sensing TRPM8 channel triggers UCPI-dependent thermogenesis and prevents obesity. (2012) Journal of Molecular Cell Biology. 4: 88-96
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[2]Ma et al. Activation of the cold-sensing TRPM8 channel triggers UCPI-dependent thermogenesis and prevents obesity. (2012) Journal of Molecular Cell Biology. 4: 88-96
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Revision as of 13:00, 7 May 2013

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Project Description/Abstract

This project will focus on harnessing the power of bacteria to generate heat by turning on and off gene expression and ultimately overepxressing one of the uncoupling proteins involved in deregulating oxidative phosphorylation.

Members of the TRP family, specifically TRPM8 and TRPV4, regulate oxidative phosphorylation via uncoupling protein 1 (UCP1). TRPM8 positively regulates UCP1 and TRPV4 negatively regulates it via inhibition of PGC1-alpha. Uncoupling protein 1 is a major source of thermogenesis, and overexpression of this protein has provided hope for treating obesity and other metabolic conditions. However, the thermogenesis potential of this protein may itself be used as a local heating source, if overexpressed to an appropriate extent. We propose seeding bacteria in a cell and overexpressing UCP1 via TRPV4 inhibition and TRPM8 activation. We believe that this will increase heat production in bacteria, which can be used in a variety of applications.

Background Information

TRPV4 negatively regulates UCP1[1] TRPM8 positively regulates UCP1[2]

Project details and methods

Insert methods here

Predicted Outcomes

Increased thermogenesis by activation of UCP1

Needed Resources

Bacteria TRPV4 shRNA

References

[1]Ye et al. TRPV4 Is a Regulator of Adipose Oxidative Metabolism, Inflammation, and Energy Homeostasis.(2012) Cell Press.151(1): 96-110

[2]Ma et al. Activation of the cold-sensing TRPM8 channel triggers UCPI-dependent thermogenesis and prevents obesity. (2012) Journal of Molecular Cell Biology. 4: 88-96

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