Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/118206
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dc.creatorMoreira, D
dc.creatorSilvestre, R
dc.creatorCordeiro-da-Silva, A
dc.creatorEstaquier, J
dc.creatorForetz, M
dc.creatorViollet, B
dc.date.accessioned2019-01-08T10:27:09Z-
dc.date.available2019-01-08T10:27:09Z-
dc.date.issued2016
dc.identifier.issn1389-4501
dc.identifier.urihttps://repositorio-aberto.up.pt/handle/10216/118206-
dc.description.abstractIntracellular pathogens are known to manipulate host cell regulatory pathways to establish an optimal environment for their growth and survival. Pathogens employ active mechanisms to hijack host cell metabolism and acquire existing nutrient and energy store. The role of the cellular energy sensor AMP-activated protein kinase (AMPK) in the regulation of cellular energy homeostasis is well documented. Here, we highlight recent advances showing the importance of AMPK signaling in pathogen-host interactions. Pathogens interact with AMPK by a variety of mechanisms aimed at reprogramming host cell metabolism to their own benefit. Stimulation of AMPK activity provides an efficient process to rapidly adapt pathogen metabolism to the major nutritional changes often encountered during the different phases of infection. However, inhibition of AMPK is also used by pathogens to manipulate innate host response, indicating that AMPK appears relevant to restriction of pathogen infection. We also document the effects of pharma cological AMPK modulators on pathogen proliferation and survival. This review illustrates intricate pathogen-AMPK interactions that may be exploited to the development of novel anti-pathogen therapies.
dc.description.sponsorshipThis work was supported by grants from INSERM, CNRS and Université Paris Descartes. BV and MF are working in the Département Hospitalo-Universitaire (DHU) AUToimmune and HORmonal diseaseS. JE acknowledges the support of the Canada Research Chair program. JE and ABC received funding from the European Community's Seventh Framework Programme under grant agreement No. 602773 (Project KINDRED). DM is supported by SFRH/ BD/91543/2012. RS thank FCT -Foundation for Science and Technology- for their Investigator FCT Grant (IF/00021/2014).
dc.language.isoeng
dc.publisherBentham Science Publishers
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F91543%2F2012/PT
dc.relation.ispartofCurrent Drug Targets, vol.17(8), p. 942-953
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/
dc.subject.meshAMP-Activated Protein Kinases/antagonists & inhibitors
dc.subject.meshAMP-Activated Protein Kinases/chemistry
dc.subject.meshAMP-Activated Protein Kinases/metabolism
dc.subject.meshAnimals
dc.subject.meshAnti-Infective Agents/pharmacology
dc.subject.meshBacterial Physiological Phenomena/drug effects
dc.subject.meshCommunicable Diseases/enzymology
dc.subject.meshCommunicable Diseases/microbiology
dc.subject.meshCommunicable Diseases/parasitology
dc.subject.meshEnergy Metabolism
dc.subject.meshEnzyme Activation
dc.subject.meshHomeostasis
dc.subject.meshHost-Pathogen Interactions
dc.subject.meshHumans
dc.subject.meshImmunity, Innate
dc.subject.meshParasites/drug effects
dc.subject.meshParasites/physiology
dc.subject.meshPhosphorylation
dc.subject.meshProtein Interaction Maps
dc.subject.meshSignal Transduction
dc.subject.meshVirus Physiological Phenomena/drug effects
dc.titleAMP-activated protein kinase as a target for pathogens: Friends or foes?
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.2174/1389450116666150416120559
dc.relation.publisherversionhttp://www.eurekaselect.com/130416/article
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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