0000000000530924

AUTHOR

Tamara Lapeña-luzón

showing 4 related works from this author

Disarrangement of Endoplasmic reticulum-mitochondria communication impairs Ca2+ homeostasis in FRDA

2020

AbstractFriedreich ataxia (FRDA) is a neurodegenerative disorder characterized by neuromuscular and neurological manifestations. It is caused by mutations in gene FXN, which results in loss of the mitochondrial protein frataxin. Endoplasmic Reticulum-mitochondria associated membranes (MAMs) are inter-organelle structures involved in the regulation of essential cellular processes, including lipid metabolism and calcium signaling. In the present study, we have analyzed in both, unicellular and multicellular models of FRDA, an analysis of calcium management and of integrity of MAMs. We observed that function of MAMs is compromised in our cellular model of FRDA, which was improved upon treatmen…

0303 health sciencesbiologyEndoplasmic reticulumLipid metabolismMitochondrionbiology.organism_classification3. Good healthCell biology03 medical and health sciences0302 clinical medicineFrataxinbiology.proteinMitochondrial calcium uptakeCellular modelDrosophila melanogaster030217 neurology & neurosurgery030304 developmental biologyCalcium signaling
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Cofilin and Neurodegeneration: New Functions for an Old but Gold Protein

2021

Cofilin is an actin-binding protein that plays a major role in the regulation of actin dynamics, an essential cellular process. This protein has emerged as a crucial molecule for functions of the nervous system including motility and guidance of the neuronal growth cone, dendritic spine organization, axonal branching, and synaptic signalling. Recently, other important functions in cell biology such as apoptosis or the control of mitochondrial function have been attributed to cofilin. Moreover, novel mechanisms of cofilin function regulation have also been described. The activity of cofilin is controlled by complex regulatory mechanisms, with phosphorylation being the most important, since t…

0301 basic medicineDendritic spine organizationCellMotilityNeurosciences. Biological psychiatry. NeuropsychiatryReviewmacromolecular substancescofilinBiologyenvironment and public health03 medical and health sciences0302 clinical medicinemedicineneurodegenerative diseasescofilin–actin rodsGeneral Neurosciencemitochondrial fissionNeurodegenerationapoptosisCofilinmedicine.diseaseCell biologymicrotubule instability030104 developmental biologymedicine.anatomical_structurePhosphorylationMitochondrial fission030217 neurology & neurosurgeryFunction (biology)RC321-571Brain Sciences
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Role of Adenosine Receptors in Rare Neurodegenerative Diseases with Motor Symptoms

2021

: The approval of istradefylline, an adenosine 2A receptor (A2AR) antagonist, as an addon treatment in adult patients with Parkinson’s disease by the Food and Drug Administration (FDA) and European Medicines Agency (EMA), is the latest proof of the importance of the adenosinergic system in the nervous system. Adenosine is an endogenous purine nucleoside with a role as a modulator of both neurotransmission and the inflammatory response. As such, the expression pattern of the 4 adenosine receptors (A1R, A2AR, A2BR and A3R) and the extracellular adenosine levels have attracted great interest in the pathogenesis and possible treatment of rare neurodegenerative diseases with motor symptoms. The…

congenital hereditary and neonatal diseases and abnormalitiesbusiness.industryNeurodegenerationNeurodegenerative DiseasesCell BiologyGeneral MedicineAdenosinergicIstradefyllinemedicine.diseaseBioinformaticsBiochemistryAdenosine receptorAdenosinechemistry.chemical_compoundchemistrymedicineSpinocerebellar ataxiaAmyotrophic lateral sclerosisbusinessMolecular BiologyMachado–Joseph diseasemedicine.drugCurrent Protein & Peptide Science
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Oxidative stress modulates rearrangement of endoplasmic reticulum-mitochondria contacts and calcium dysregulation in a Friedreich's ataxia model

2020

Friedreich ataxia (FRDA) is a neurodegenerative disorder characterized by neuromuscular and neurological manifestations. It is caused by mutations in the FXN gene, which results in loss of the mitochondrial protein frataxin. Endoplasmic Reticulum-mitochondria associated membranes (MAMs) are inter-organelle structures involved in the regulation of essential cellular processes, including lipid metabolism and calcium signaling. In the present study, we have analyzed in both, unicellular and multicellular models of FRDA, calcium management and integrity of MAMs. We observed that function of MAMs is compromised in our cellular model of FRDA, which was improved upon treatment with antioxidants. I…

0301 basic medicineAtaxiaClinical BiochemistryLipid peroxidationchemistry.chemical_elementMitochondrionCalciumEndoplasmic ReticulumBiochemistry03 medical and health sciences0302 clinical medicineMAMsmedicineAnimalsVitamin EMitochondrial calcium uptakelcsh:QH301-705.5Calcium signalinglcsh:R5-920biologyFrataxinEndoplasmic reticulumOrganic ChemistryN-acetylcysteineMitochondriaCell biologyOxidative StressDrosophila melanogaster030104 developmental biologychemistrylcsh:Biology (General)Friedreich AtaxiaFrataxinbiology.proteinCalciummedicine.symptomCellular modellcsh:Medicine (General)030217 neurology & neurosurgeryResearch PaperRedox Biology
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